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390 results on '"Landström, Maréne"'

3. Fluorophore-conjugated Helicobacter pylori recombinant membrane protein (HopQ) labels primary colon cancer and metastases in orthotopic mouse models by binding CEA-related cell adhesion molecules

Author

Hollandsworth, Hannah M, Schmitt, Verena, Amirfakhri, Siamak, Filemoni, Filemoni, Schmidt, Alexej, Landström, Maréne, Lyndin, Mykola, Backert, Steffen, Gerhard, Markus, Wennemuth, Gunther, Hoffman, Robert M, Singer, Bernhard B, and Bouvet, Michael

Subjects
Cancer, Digestive Diseases, Biomedical Imaging, Colo-Rectal Cancer, Biotechnology, Biochemistry and Cell Biology, Clinical Sciences, Oncology and Carcinogenesis, Oncology & Carcinogenesis
Abstract

HopQ is an outer-membrane protein of Helicobacter pylori that binds to human carcinoembryonic antigen-related cell-adhesion molecules (CEACAMs) with high specificity. We aimed to investigate fluorescence targeting of CEACAM-expressing colorectal tumors in patient-derived orthotopic xenograft (PDOX) models with fluorescently labeled recombinant HopQ (rHopQ). Western blotting, flow cytometry and ELISA were performed to determine the efficiency of rHopQ binding to CEACAMs. rHopQ was conjugated to IR800DyeCW (rHopQ-IR800). Nude mice received orthotopic implantation of colon cancer tumors. Three weeks later, mice were administered 25 μg or 50 μg HopQ-IR800 and imaged 24 or 48 h later. Intravital images were analyzed for tumor-to-background ratio (TBR). Flow cytometry and ELISA demonstrated binding of HopQ to CEACAM1, 3 and 5. Dose-response intravital imaging in PDOX models demonstrated optimal results 48 h after administration of 50 μg rHopQ-IR800 (TBR = 3.576) in our protocol. Orthotopic models demonstrated clear tumor margins of primary tumors and small regional metastases with a mean TBR = 3.678 (SD ± 1.027). rHopQ showed specific binding to various CEACAMs in PDOX models. rHopQ may be useful for CEACAM-positive tumor and metastasis detection for pre-surgical diagnosis, intra-operative imaging and fluorescence-guided surgery.

Published
2020

4. Implementing precision medicine in a regionally organized healthcare system in Sweden

Author

Fioretos, Thoas, Wirta, Valtteri, Cavelier, Lucia, Berglund, Eva, Friedman, Mikaela, Akhras, Michael, Botling, Johan, Ehrencrona, Hans, Engstrand, Lars, Helenius, Gisela, Fagerqvist, Therese, Gisselsson, David, Gruvberger-Saal, Sofia, Gyllensten, Ulf, Heidenblad, Markus, Höglund, Kina, Jacobsson, Bo, Johansson, Maria, Johansson, Åsa, Soller, Maria Johansson, Landström, Maréne, Larsson, Pär, Levin, Lars-Åke, Lindstrand, Anna, Lovmar, Lovisa, Lyander, Anna, Melin, Malin, Nordgren, Ann, Nordmark, Gunnel, Mölling, Paula, Palmqvist, Lars, Palmqvist, Richard, Repsilber, Dirk, Sikora, Per, Stenmark, Bianca, Söderkvist, Peter, Stranneheim, Henrik, Strid, Tobias, Wheelock, Craig E., Wadelius, Mia, Wedell, Anna, Edsjö, Anders, and Rosenquist, Richard

Published
2022
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5. Human transforming growth factor β type I receptor in complex with kinase inhibitor SB505124.

Author

Rodriguez Buitrago, Jhon A., Landström, Maréne, and Wolf-Watz, Magnus

Subjects
*CELLULAR signal transduction, *HUMAN growth, *CANCER treatment, *KINASE inhibitors, *CRYSTAL structure
Abstract

The crystal structure of the intracellular domain of transforming growth factor β type I receptor (TβR1) in complex with the competitive inhibitor SB505124 is presented. The study provides insights into the structure and function of TβR1 in complex with SB505124, and as such offers molecular‐level understanding of the inhibition of this critical signalling pathway. The potential of SB505124 as an avenue for therapy in cancer treatment is discussed on basis of the results. [ABSTRACT FROM AUTHOR]

Published
2024
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6. Helicobacter pylori Adapts to Chronic Infection and Gastric Disease via pH-Responsive BabA-Mediated Adherence

Author

Bugaytsova, Jeanna A, Björnham, Oscar, Chernov, Yevgen A, Gideonsson, Pär, Henriksson, Sara, Mendez, Melissa, Sjöström, Rolf, Mahdavi, Jafar, Shevtsova, Anna, Ilver, Dag, Moonens, Kristof, Quintana-Hayashi, Macarena P, Moskalenko, Roman, Aisenbrey, Christopher, Bylund, Göran, Schmidt, Alexej, Åberg, Anna, Brännström, Kristoffer, Königer, Verena, Vikström, Susanne, Rakhimova, Lena, Hofer, Anders, Ögren, Johan, Liu, Hui, Goldman, Matthew D, Whitmire, Jeannette M, Ådén, Jörgen, Younson, Justine, Kelly, Charles G, Gilman, Robert H, Chowdhury, Abhijit, Mukhopadhyay, Asish K, Nair, G Balakrish, Papadakos, Konstantinos S, Martinez-Gonzalez, Beatriz, Sgouras, Dionyssios N, Engstrand, Lars, Unemo, Magnus, Danielsson, Dan, Suerbaum, Sebastian, Oscarson, Stefan, Morozova-Roche, Ludmilla A, Olofsson, Anders, Gröbner, Gerhard, Holgersson, Jan, Esberg, Anders, Strömberg, Nicklas, Landström, Maréne, Eldridge, Angela M, Chromy, Brett A, Hansen, Lori M, Solnick, Jay V, Lindén, Sara K, Haas, Rainer, Dubois, Andre, Merrell, D Scott, Schedin, Staffan, Remaut, Han, Arnqvist, Anna, Berg, Douglas E, and Borén, Thomas

Subjects
Medical Microbiology, Biomedical and Clinical Sciences, Biological Sciences, Emerging Infectious Diseases, Infectious Diseases, Prevention, Digestive Diseases, Digestive Diseases - (Peptic Ulcer), Biodefense, Vaccine Related, Adhesins, Bacterial, Bacterial Adhesion, Gastric Mucosa, Helicobacter Infections, Helicobacter pylori, Hydrogen-Ion Concentration, acid responsiveness, adaptation, blood group antigen-binding adhesion, diversity, gastric acidity, gastric cancer, multimerization, polymorphism, subpopulations, Microbiology, Immunology, Biochemistry and cell biology, Medical microbiology
Abstract

The BabA adhesin mediates high-affinity binding of Helicobacter pylori to the ABO blood group antigen-glycosylated gastric mucosa. Here we show that BabA is acid responsive-binding is reduced at low pH and restored by acid neutralization. Acid responsiveness differs among strains; often correlates with different intragastric regions and evolves during chronic infection and disease progression; and depends on pH sensor sequences in BabA and on pH reversible formation of high-affinity binding BabA multimers. We propose that BabA's extraordinary reversible acid responsiveness enables tight mucosal bacterial adherence while also allowing an effective escape from epithelial cells and mucus that are shed into the acidic bactericidal lumen and that bio-selection and changes in BabA binding properties through mutation and recombination with babA-related genes are selected by differences among individuals and by changes in gastric acidity over time. These processes generate diverse H. pylori subpopulations, in which BabA's adaptive evolution contributes to H. pylori persistence and overt gastric disease.

Published
2017

7. Changing smoking habits and the occurrence of lung cancer in Sweden : a population analysis

Author

Järvholm, Bengt, Hedman, Linnea, Landström, Maréne, Liv, Per, Burdorf, Alex, Toren, Kjell, Järvholm, Bengt, Hedman, Linnea, Landström, Maréne, Liv, Per, Burdorf, Alex, and Toren, Kjell

Abstract

Background: The objective is to estimate the importance of the decrease of smoking habits in Sweden for the occurrence of lung cancer. Methods: The change in smoking habits in the general population was retrieved from surveys and on taxation of sale of cigarettes. We used data from the Swedish Cancer Register on incidence of lung cancer between 1970 and 2021, stratified for sex, age and cell type, and compared the occurrence overtime in ages between 40 and 84 years. Results: The sale of cigarettes peaked in 1980 to 1800 cigarettes per person and decreased to 600 per person in 2021. The change in incidence rates of squamous cell cancer and other cell types varied over time, sex, and age in a pattern that partly seems to be explained by change in the prevalence of daily smokers. The incidence of adenocarcinoma was similar in men and women 1970–2021 and increased, e.g. for women and men 75–79 years of age from around 20 cases in early 1970s to around 120 cases per 100 000 person-years in the 2020s. Conclusions: Our data indicate that the risk of lung cancer several years after smoking cessation is less favourable than previously studies have indicated. There is a similar increase in the incidence of adenocarcinoma in men and women which is hard to explain only with changing smoking habits. The change from non-filter to filter cigarettes in the 1960s–1970s may be a contributing factor.

Published
2024
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9. TRAF6

Author

Sundar, Reshma, Landström, Maréne, and Choi, Sangdun, editor

Published
2018
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12. Exploring the impact of oral bacteria remnants on stem cells from the Apical papilla : mineralization potential and inflammatory response

Author

Zymovets, Valeriia, Rakhimova, Olena, Wadelius, Philip, Schmidt, Alexej, Brundin, Malin, Kelk, Peyman, Landström, Maréne, Romani Vestman, Nelly, Zymovets, Valeriia, Rakhimova, Olena, Wadelius, Philip, Schmidt, Alexej, Brundin, Malin, Kelk, Peyman, Landström, Maréne, and Romani Vestman, Nelly

Abstract

Introduction: Bacterial persistence is considered one of the main causal factors for regenerative endodontic treatment (RET) failure in immature permanent teeth. This interference is claimed to be caused by the interaction of bacteria that reside in the root canal with the stem cells that are one of the essentials for RET. The aim of the study was to investigate whether prolonged exposure of stem cells from the apical papilla (SCAP) to bacterial remnants of Fusobacterium nucleatum, Actinomyces gerensceriae, Slackia exigua, Enterococcus faecalis, Peptostreptococcaceae yurii, commonly found in infected traumatized root canals, and the probiotic bacteria Lactobacillus gasseri and Limosilactobacillus reuteri, can alter SCAP’s inflammatory response and mineralization potential. Methods: To assess the effect of bacterial remnants on SCAP, we used UV-C–inactivated bacteria (as cell wall-associated virulence factors) and bacterial DNA. Histochemical staining using Osteoimage Mineralization Assay and Alizarin Red analysis was performed to study SCAP mineralization, while inflammatory and osteo/odontogenic-related responses of SCAPs were assessed with Multiplex ELISA. Results: We showed that mineralization promotion was greater with UV C–inactivated bacteria compared to bacterial DNA. Immunofluorescence analysis detected that the early mineralization marker alkaline phosphatase (ALP) was increased by the level of E. coli lipopolysaccharide (LPS) positive control in the case of UV-C–inactivated bacteria; meanwhile, DNA treatment decreased the level of ALP compared to the positive control. SCAP’s secretome assessed with Multiplex ELISA showed the upregulation of pro-inflammatory factors IL-6, IL-8, GM-CSF, IL-1b, neurotrophic factor BDNF, and angiogenic factor VEGF, induced by UV-C–killed bacteria. Discussion: The results suggest that long term stimulation (for 21 days) of SCAP with UV-C–inactivated bacteria stimulate their mineralization and inflammatory response, while DNA in

Published
2023
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14. Trailblazing precision medicine in Europe: A joint view by Genomic Medicine Sweden and the Centers for Personalized Medicine, ZPM, in Germany

Author

Stenzinger, Albrecht, primary, Edsjö, Anders, additional, Ploeger, Carolin, additional, Friedman, Mikaela, additional, Fröhling, Stefan, additional, Wirta, Valtteri, additional, Seufferlein, Thomas, additional, Botling, Johan, additional, Duyster, Justus, additional, Akhras, Michael, additional, Thimme, Robert, additional, Fioretos, Thoas, additional, Bitzer, Michael, additional, Cavelier, Lucia, additional, Schirmacher, Peter, additional, Malek, Nisar, additional, Rosenquist, Richard, additional, Lindstrand, Anna, additional, Wedell, Anna, additional, Gisselsson, David, additional, Melén, Erik, additional, Helenius, Gisela, additional, Ehrencrona, Hans, additional, Engstrand, Lars, additional, Palmqvist, Lars, additional, Levin, Lars-Åke, additional, Lovmar, Lovisa, additional, Landström, Maréne, additional, Hallbeck, Martin, additional, Wadelius, Mia, additional, Sikora, Per, additional, Beer, Ambros J., additional, Illert, Anna L., additional, Budczies, Jan, additional, Nikolaou, Konstantin, additional, Kohlbacher, Oliver, additional, Horak, Peter, additional, Kuhn, Peter, additional, Schroeder, Christopher, additional, Boerries, Melanie, additional, Lassmann, Silke, additional, and Gaidzik, Verena I., additional

Published
2022
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18. TRAF6

Author

Sundar, Reshma, primary and Landström, Maréne, additional

Published
2016
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19. The Synergistic Cooperation between TGF-Cancer and Fibrosis

Author

Mallikarjuna, Pramod, Zhou, Yang, and Landström, Maréne

Subjects
TGF-β, Cancer och onkologi, hypoxia, Cancer and Oncology, fibrosis, cancer, HIF-1α/2α, TRAF6, Smad
Abstract

Transforming growth factor β (TGF-β) is a multifunctional cytokine regulating homeostasis and immune responses in adult animals and humans. Aberrant and overactive TGF-β signaling promotes cancer initiation and fibrosis through epithelial–mesenchymal transition (EMT), as well as the invasion and metastatic growth of cancer cells. TGF-β is a key factor that is active during hypoxic conditions in cancer and is thereby capable of contributing to angiogenesis in various types of cancer. Another potent role of TGF-β is suppressing immune responses in cancer patients. The strong tumor-promoting effects of TGF-β and its profibrotic effects make it a focus for the development of novel therapeutic strategies against cancer and fibrosis as well as an attractive drug target in combination with immune regulatory checkpoint inhibitors. TGF-β belongs to a family of cytokines that exert their function through signaling via serine/threonine kinase transmembrane receptors to intracellular Smad proteins via the canonical pathway and in combination with co-regulators such as the adaptor protein and E3 ubiquitin ligases TRAF4 and TRAF6 to promote non-canonical pathways. Finally, the outcome of gene transcription initiated by TGF-β is context-dependent and controlled by signals exerted by other growth factors such as EGF and Wnt. Here, we discuss the synergistic cooperation between TGF-β and hypoxia in development, fibrosis and cancer.

Published
2022

20. The type II TGF-β receptor phosphorylates Tyr182 in the type I receptor to activate downstream Src signaling.

Author

Yakymovych, Ihor, Yakymovych, Mariya, Hamidi, Anahita, Landström, Maréne, and Heldin, Carl-Henrik

Subjects
PROTEIN-tyrosine kinases, KINASES, FETAL tissues, EMBRYOLOGY, FIBRONECTINS, CELL migration, AUTOPHOSPHORYLATION, PROLINE, MYOFIBROBLASTS
Abstract

Transforming growth factor–β (TGF-β) signaling has important roles during embryonic development and in tissue homeostasis. TGF-β ligands exert cellular effects by binding to type I (TβRI) and type II (TβRII) receptors and inducing both SMAD-dependent and SMAD-independent intracellular signaling pathways, the latter of which includes the activation of the tyrosine kinase Src. We investigated the mechanism by which TGF-β stimulation activates Src in human and mouse cells. Before TGF-β stimulation, inactive Src was complexed with TβRII. Upon TGF-β1 stimulation, TβRII associated with and phosphorylated TβRI at Tyr182. Binding of Src to TβRI involved the interaction of the Src SH2 domain with phosphorylated Tyr182 and the interaction of the Src SH3 domain with a proline-rich region in TβRI and led to the activation of Src kinase activity and Src autophosphorylation. TGF-β1–induced Src activation required the kinase activities of TβRII and Src but not that of TβRI. Activated Src also phosphorylated TβRI on several tyrosine residues, which may stabilize the binding of Src to the receptor. Src activation was required for the ability of TGF-β to induce fibronectin production and migration in human breast carcinoma cells and to induce α–smooth muscle actin and actin reorganization in mouse fibroblasts. Thus, TGF-β induces Src activation by stimulating a direct interaction with TβRI that depends on tyrosine phosphorylation of TβRI by TβRII. How TGF-β activates Src: TGF-β signaling is critical for development and homeostasis, and its dysregulation contributes to various diseases. The binding of TGF-β ligands to their receptors, TβRI and TβRII, induces the activation of multiple intracellular signaling mediators, including the tyrosine kinase Src. Yakymovych et al. demonstrated that TGF-β1 stimulated Src activation through a mechanism that depended on tyrosine phosphorylation of TβRI by TβRII, leading to Src recruitment to TβRI and Src autophosphorylation. Activation of Src was required for the responses of human and mouse cells to TGF-β stimulation. These findings elucidate the mechanism by which TGF-β induces Src activation. [ABSTRACT FROM AUTHOR]

Published
2022
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21. Significance of PI3K Signalling pathway in clear cell renal cell carcinoma in relation to VHL and HIF status

Author

Tumkur Sitaram, Raviprakash, Landström, Maréne, Roos, Göran, Ljungberg, Börje, Tumkur Sitaram, Raviprakash, Landström, Maréne, Roos, Göran, and Ljungberg, Börje

Abstract

Renal cell carcinoma (RCC) includes diverse tumor types characterized by various genetic abnormalities. The genetic changes, like mutations, deletions, and epigenetic alterations, play a crucial role in the modification of signaling networks, tumor pathogenesis, and prognosis. The most prevalent RCC type, clear cell RCC (ccRCC), is asymptomatic in the early stages and has a poorer prognosis compared with the papillary and the chromophobe typesRCCs. Generally, ccRCC is refractory to chemotherapy and radiation therapy. Loss of VHL gene and upregulation of hypoxia-inducible factors (HIF), the signature of most sporadic ccRCC, promote multiple growth factors. Hence, VHL/HIF and a variety of pathways, including PTEN/PI3K/AKT, are closely connected and contribute to the ontogeny of ccRCC. In the recent decade, multiple targeting agents have been developed based on blocking major signaling pathways directly or indirectly involved in ccRCC tumor progression, metastasis, angiogenesis, and survival. However, most of these drugs have limitations; either metastatic ccRCC develops resistance to these agents, or despite blocking receptors, tumor cells utilize alternate signaling pathways. This review compiles the state of knowledge about the PI3K/AKT signaling pathway confined to ccRCC and their cross-talks with VHL/HIF pathways.

Published
2021
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23. Fluorophore-conjugated Helicobacter pylori recombinant membrane protein (HopQ) labels primary colon cancer and metastases in orthotopic mouse models by binding CEA-related cell adhesion molecules

Author

Hollandsworth, Hannah M., Schmitt, Verena, Amirfakhri, Siamak, Filemoni, Filemoni, Schmidt, Alexej, Landström, Maréne, Lyndin, Mykola, Backert, Steffen, Gerhard, Markus, Wennemuth, Gunther, Hoffman, Robert M., Singer, Bernhard B., Bouvet, Michael, Hollandsworth, Hannah M., Schmitt, Verena, Amirfakhri, Siamak, Filemoni, Filemoni, Schmidt, Alexej, Landström, Maréne, Lyndin, Mykola, Backert, Steffen, Gerhard, Markus, Wennemuth, Gunther, Hoffman, Robert M., Singer, Bernhard B., and Bouvet, Michael

Abstract

HopQ is an outer-membrane protein of Helicobacter pylori that binds to human carcinoembryonic antigen-related cell-adhesion molecules (CEACAMs) with high specificity. We aimed to investigate fluorescence targeting of CEACAM-expressing colorectal tumors in patient-derived orthotopic xenograft (PDOX) models with fluorescently labeled recombinant HopQ (rHopQ). Western blotting, flow cytometry and ELISA were performed to determine the efficiency of rHopQ binding to CEACAMs. rHopQ was conjugated to IR800DyeCW (rHopQ-IR800). Nude mice received orthotopic implantation of colon cancer tumors. Three weeks later, mice were administered 25 μg or 50 μg HopQ-IR800 and imaged 24 or 48 h later. Intravital images were analyzed for tumor-to-background ratio (TBR). Flow cytometry and ELISA demonstrated binding of HopQ to CEACAM1, 3 and 5. Dose-response intravital imaging in PDOX models demonstrated optimal results 48 h after administration of 50 μg rHopQ-IR800 (TBR = 3.576) in our protocol. Orthotopic models demonstrated clear tumor margins of primary tumors and small regional metastases with a mean TBR = 3.678 (SD ± 1.027). rHopQ showed specific binding to various CEACAMs in PDOX models. rHopQ may be useful for CEACAM-positive tumor and metastasis detection for pre-surgical diagnosis, intra-operative imaging and fluorescence-guided surgery.

Published
2020
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24. Role of Wnt Signaling Pathways in Clear Cell Renal Cell Carcinoma Pathogenesis in Relation to VHL and HIF Status

Author

Tumkur Sitaram, Raviprakash, Landström, Maréne, Roos, Göran, Ljungberg, Börje, Tumkur Sitaram, Raviprakash, Landström, Maréne, Roos, Göran, and Ljungberg, Börje

Abstract

Renal cell carcinoma (RCC) encompasses various tumor types characterized by a variety of genetic abnormalities. The genetic changes, like mutations, deletions, and epigenetic alterations, can affect the signaling components and signaling networks, causing the modification of tumor pathogenesis and prognosis of RCC. The most prevalent RCC, clear cell RCC (ccRCC), is asymptomatic in the early stages, refractory to chemotherapy and radiation therapy, and has a poorer prognosis compared with the papillary and chromophobe ccRCC types. Loss of the VHL gene and upregulation of oxygen sensors, hypoxia-inducible factor alphas (HIF-α), which promote different growth factors, is a signature of sporadic ccRCC. The VHL-HIF-α and Wnt/β-catenin pathways are closely connected and contribute to the ontogeny of ccRCC. This review confines to ccRCC and the role of the Wnt/β-catenin signaling pathways and its crosstalk with VHL/HIF.

Published
2020
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25. Cytokine Secretion, Viability, and Real-Time Proliferation of Apical-Papilla Stem Cells Upon Exposure to Oral Bacteria

Author

Rakhimova, Olena, Schmidt, Alexej, Landström, Maréne, Johansson, Anders, Kelk, Peyman, Romani Vestman, Nelly, Rakhimova, Olena, Schmidt, Alexej, Landström, Maréne, Johansson, Anders, Kelk, Peyman, and Romani Vestman, Nelly

Abstract

The use of stem cells from the apical papilla (SCAPs) has been proposed as a means of promoting root maturation in permanent immature teeth, and plays a significant role in regenerative dental procedures. However, the role of SCAPs may be compromised by microenvironmental factors, such as hypoxic conditions and the presence of bacteria from infected dental root canals. We aim to investigate oral bacterial modulation of SCAP in terms of binding capacity using flow cytometry and imaging, real-time cell proliferation monitoring, and cytokine secretion (IL-6, IL-8, and TGF-β isoforms) under anaerobic conditions. SCAPs were exposed to key species in dental root canal infection, namely Actinomyces gerensceriae, Slackia exigua, Fusobacterium nucleatum, and Enterococcus faecalis, as well as two probiotic strains, Lactobacillus gasseri strain B6 and Lactobacillus reuteri (DSM 17938). We found that A. gerensceriae, S. exigua, F. nucleatum, and E. faecalis, but not the Lactobacillus probiotic strains bind to SCAPs on anaerobic conditions. Enterococcus faecalis and F. nucleatum exhibited the strongest binding capacity, resulting in significantly reduced SCAP proliferation. Notably, F. nucleatum, but not E. faecalis, induce production of the proinflammatory chemokine IL-8 and IL-10 from SCAPs. Production of TGF-β1 and TGF-β2 by SCAPs was dependent on species, cell line, and time, but secretion of TGF-β3 did not vary significantly over time. In conclusion, SCAP response is compromised when exposed to bacterial stimuli from infected dental root canals in anaerobic conditions. Thus, stem cell-mediated endodontic regenerative studies need to include microenvironmental conditions, such as the presence of microorganisms to promote further advantage in the field.

Published
2020
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27. TMEM85 (Transmembrane Protein 85)

Author

Gonçalves, João, primary, Soares, Helena, additional, Eberhardt, Norman L., additional, Lummis, Sarah C. R., additional, Soto-Pantoja, David R., additional, Roberts, David D., additional, Maitra, Umadas, additional, Majumdar, Romit, additional, Biswas, Arunima, additional, Choudhuri, Avik, additional, Krishnan, Jayalakshmi, additional, Choi, Sangdun, additional, Atif, Shaikh M., additional, McSorley, Stephen J., additional, Greenwood, Michael T., additional, Butt, Aisha Qasim, additional, Miggin, Sinéad M., additional, Tuon, Felipe Francisco, additional, Shevlin, Enda, additional, Della-Franca, Austin, additional, Chen, Yuyan, additional, Byrne, Jennifer Anne, additional, Virla, Dimitra, additional, Tsatsanis, Christos, additional, Eliopoulos, Aristides G., additional, Landström, Maréne, additional, Sundar, Reshma, additional, Sung, Eun-Sil, additional, Kim, Yong-Sung, additional, Angyal, Adrienn, additional, Kiss-Toth, Endre, additional, and Harteneck, Christian, additional

Published
2012
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28. TRAIL-R2 (Tumor Necrosis Factor-Related Apoptosis-Inducing Ligand Receptor 2)

Author

Gonçalves, João, primary, Soares, Helena, additional, Eberhardt, Norman L., additional, Lummis, Sarah C. R., additional, Soto-Pantoja, David R., additional, Roberts, David D., additional, Maitra, Umadas, additional, Majumdar, Romit, additional, Biswas, Arunima, additional, Choudhuri, Avik, additional, Krishnan, Jayalakshmi, additional, Choi, Sangdun, additional, Atif, Shaikh M., additional, McSorley, Stephen J., additional, Greenwood, Michael T., additional, Butt, Aisha Qasim, additional, Miggin, Sinéad M., additional, Tuon, Felipe Francisco, additional, Shevlin, Enda, additional, Della-Franca, Austin, additional, Chen, Yuyan, additional, Byrne, Jennifer Anne, additional, Virla, Dimitra, additional, Tsatsanis, Christos, additional, Eliopoulos, Aristides G., additional, Landström, Maréne, additional, Sundar, Reshma, additional, Sung, Eun-Sil, additional, Kim, Yong-Sung, additional, Angyal, Adrienn, additional, Kiss-Toth, Endre, additional, and Harteneck, Christian, additional

Published
2012
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29. TOB2 (Transducer of ERBB2 2)

Author

Gonçalves, João, primary, Soares, Helena, additional, Eberhardt, Norman L., additional, Lummis, Sarah C. R., additional, Soto-Pantoja, David R., additional, Roberts, David D., additional, Maitra, Umadas, additional, Majumdar, Romit, additional, Biswas, Arunima, additional, Choudhuri, Avik, additional, Krishnan, Jayalakshmi, additional, Choi, Sangdun, additional, Atif, Shaikh M., additional, McSorley, Stephen J., additional, Greenwood, Michael T., additional, Butt, Aisha Qasim, additional, Miggin, Sinéad M., additional, Tuon, Felipe Francisco, additional, Shevlin, Enda, additional, Della-Franca, Austin, additional, Chen, Yuyan, additional, Byrne, Jennifer Anne, additional, Virla, Dimitra, additional, Tsatsanis, Christos, additional, Eliopoulos, Aristides G., additional, Landström, Maréne, additional, Sundar, Reshma, additional, Sung, Eun-Sil, additional, Kim, Yong-Sung, additional, Angyal, Adrienn, additional, Kiss-Toth, Endre, additional, and Harteneck, Christian, additional

Published
2012
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30. T16

Author

Gonçalves, João, primary, Soares, Helena, additional, Eberhardt, Norman L., additional, Lummis, Sarah C. R., additional, Soto-Pantoja, David R., additional, Roberts, David D., additional, Maitra, Umadas, additional, Majumdar, Romit, additional, Biswas, Arunima, additional, Choudhuri, Avik, additional, Krishnan, Jayalakshmi, additional, Choi, Sangdun, additional, Atif, Shaikh M., additional, McSorley, Stephen J., additional, Greenwood, Michael T., additional, Butt, Aisha Qasim, additional, Miggin, Sinéad M., additional, Tuon, Felipe Francisco, additional, Shevlin, Enda, additional, Della-Franca, Austin, additional, Chen, Yuyan, additional, Byrne, Jennifer Anne, additional, Virla, Dimitra, additional, Tsatsanis, Christos, additional, Eliopoulos, Aristides G., additional, Landström, Maréne, additional, Sundar, Reshma, additional, Sung, Eun-Sil, additional, Kim, Yong-Sung, additional, Angyal, Adrienn, additional, Kiss-Toth, Endre, additional, and Harteneck, Christian, additional

Published
2012
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31. TNFα (Tumor Necrosis Factor α)

Author

Gonçalves, João, primary, Soares, Helena, additional, Eberhardt, Norman L., additional, Lummis, Sarah C. R., additional, Soto-Pantoja, David R., additional, Roberts, David D., additional, Maitra, Umadas, additional, Majumdar, Romit, additional, Biswas, Arunima, additional, Choudhuri, Avik, additional, Krishnan, Jayalakshmi, additional, Choi, Sangdun, additional, Atif, Shaikh M., additional, McSorley, Stephen J., additional, Greenwood, Michael T., additional, Butt, Aisha Qasim, additional, Miggin, Sinéad M., additional, Tuon, Felipe Francisco, additional, Shevlin, Enda, additional, Della-Franca, Austin, additional, Chen, Yuyan, additional, Byrne, Jennifer Anne, additional, Virla, Dimitra, additional, Tsatsanis, Christos, additional, Eliopoulos, Aristides G., additional, Landström, Maréne, additional, Sundar, Reshma, additional, Sung, Eun-Sil, additional, Kim, Yong-Sung, additional, Angyal, Adrienn, additional, Kiss-Toth, Endre, additional, and Harteneck, Christian, additional

Published
2012
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32. TRIF: TIR Domain–Containing Adaptor-Inducing Interferon β

Author

Gonçalves, João, primary, Soares, Helena, additional, Eberhardt, Norman L., additional, Lummis, Sarah C. R., additional, Soto-Pantoja, David R., additional, Roberts, David D., additional, Maitra, Umadas, additional, Majumdar, Romit, additional, Biswas, Arunima, additional, Choudhuri, Avik, additional, Krishnan, Jayalakshmi, additional, Choi, Sangdun, additional, Atif, Shaikh M., additional, McSorley, Stephen J., additional, Greenwood, Michael T., additional, Butt, Aisha Qasim, additional, Miggin, Sinéad M., additional, Tuon, Felipe Francisco, additional, Shevlin, Enda, additional, Della-Franca, Austin, additional, Chen, Yuyan, additional, Byrne, Jennifer Anne, additional, Virla, Dimitra, additional, Tsatsanis, Christos, additional, Eliopoulos, Aristides G., additional, Landström, Maréne, additional, Sundar, Reshma, additional, Sung, Eun-Sil, additional, Kim, Yong-Sung, additional, Angyal, Adrienn, additional, Kiss-Toth, Endre, additional, and Harteneck, Christian, additional

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2012
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33. TEAD-4

Author

Gonçalves, João, primary, Soares, Helena, additional, Eberhardt, Norman L., additional, Lummis, Sarah C. R., additional, Soto-Pantoja, David R., additional, Roberts, David D., additional, Maitra, Umadas, additional, Majumdar, Romit, additional, Biswas, Arunima, additional, Choudhuri, Avik, additional, Krishnan, Jayalakshmi, additional, Choi, Sangdun, additional, Atif, Shaikh M., additional, McSorley, Stephen J., additional, Greenwood, Michael T., additional, Butt, Aisha Qasim, additional, Miggin, Sinéad M., additional, Tuon, Felipe Francisco, additional, Shevlin, Enda, additional, Della-Franca, Austin, additional, Chen, Yuyan, additional, Byrne, Jennifer Anne, additional, Virla, Dimitra, additional, Tsatsanis, Christos, additional, Eliopoulos, Aristides G., additional, Landström, Maréne, additional, Sundar, Reshma, additional, Sung, Eun-Sil, additional, Kim, Yong-Sung, additional, Angyal, Adrienn, additional, Kiss-Toth, Endre, additional, and Harteneck, Christian, additional

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2012
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34. Tripartite Motif Protein 23

Author

Gonçalves, João, primary, Soares, Helena, additional, Eberhardt, Norman L., additional, Lummis, Sarah C. R., additional, Soto-Pantoja, David R., additional, Roberts, David D., additional, Maitra, Umadas, additional, Majumdar, Romit, additional, Biswas, Arunima, additional, Choudhuri, Avik, additional, Krishnan, Jayalakshmi, additional, Choi, Sangdun, additional, Atif, Shaikh M., additional, McSorley, Stephen J., additional, Greenwood, Michael T., additional, Butt, Aisha Qasim, additional, Miggin, Sinéad M., additional, Tuon, Felipe Francisco, additional, Shevlin, Enda, additional, Della-Franca, Austin, additional, Chen, Yuyan, additional, Byrne, Jennifer Anne, additional, Virla, Dimitra, additional, Tsatsanis, Christos, additional, Eliopoulos, Aristides G., additional, Landström, Maréne, additional, Sundar, Reshma, additional, Sung, Eun-Sil, additional, Kim, Yong-Sung, additional, Angyal, Adrienn, additional, Kiss-Toth, Endre, additional, and Harteneck, Christian, additional

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2012
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35. Testis Determining Factor

Author

Gonçalves, João, primary, Soares, Helena, additional, Eberhardt, Norman L., additional, Lummis, Sarah C. R., additional, Soto-Pantoja, David R., additional, Roberts, David D., additional, Maitra, Umadas, additional, Majumdar, Romit, additional, Biswas, Arunima, additional, Choudhuri, Avik, additional, Krishnan, Jayalakshmi, additional, Choi, Sangdun, additional, Atif, Shaikh M., additional, McSorley, Stephen J., additional, Greenwood, Michael T., additional, Butt, Aisha Qasim, additional, Miggin, Sinéad M., additional, Tuon, Felipe Francisco, additional, Shevlin, Enda, additional, Della-Franca, Austin, additional, Chen, Yuyan, additional, Byrne, Jennifer Anne, additional, Virla, Dimitra, additional, Tsatsanis, Christos, additional, Eliopoulos, Aristides G., additional, Landström, Maréne, additional, Sundar, Reshma, additional, Sung, Eun-Sil, additional, Kim, Yong-Sung, additional, Angyal, Adrienn, additional, Kiss-Toth, Endre, additional, and Harteneck, Christian, additional

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2012
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36. TLR4, Toll-Like Receptor 4

Author

Gonçalves, João, primary, Soares, Helena, additional, Eberhardt, Norman L., additional, Lummis, Sarah C. R., additional, Soto-Pantoja, David R., additional, Roberts, David D., additional, Maitra, Umadas, additional, Majumdar, Romit, additional, Biswas, Arunima, additional, Choudhuri, Avik, additional, Krishnan, Jayalakshmi, additional, Choi, Sangdun, additional, Atif, Shaikh M., additional, McSorley, Stephen J., additional, Greenwood, Michael T., additional, Butt, Aisha Qasim, additional, Miggin, Sinéad M., additional, Tuon, Felipe Francisco, additional, Shevlin, Enda, additional, Della-Franca, Austin, additional, Chen, Yuyan, additional, Byrne, Jennifer Anne, additional, Virla, Dimitra, additional, Tsatsanis, Christos, additional, Eliopoulos, Aristides G., additional, Landström, Maréne, additional, Sundar, Reshma, additional, Sung, Eun-Sil, additional, Kim, Yong-Sung, additional, Angyal, Adrienn, additional, Kiss-Toth, Endre, additional, and Harteneck, Christian, additional

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2012
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37. Tyro4 (Rat)

Author

Gonçalves, João, primary, Soares, Helena, additional, Eberhardt, Norman L., additional, Lummis, Sarah C. R., additional, Soto-Pantoja, David R., additional, Roberts, David D., additional, Maitra, Umadas, additional, Majumdar, Romit, additional, Biswas, Arunima, additional, Choudhuri, Avik, additional, Krishnan, Jayalakshmi, additional, Choi, Sangdun, additional, Atif, Shaikh M., additional, McSorley, Stephen J., additional, Greenwood, Michael T., additional, Butt, Aisha Qasim, additional, Miggin, Sinéad M., additional, Tuon, Felipe Francisco, additional, Shevlin, Enda, additional, Della-Franca, Austin, additional, Chen, Yuyan, additional, Byrne, Jennifer Anne, additional, Virla, Dimitra, additional, Tsatsanis, Christos, additional, Eliopoulos, Aristides G., additional, Landström, Maréne, additional, Sundar, Reshma, additional, Sung, Eun-Sil, additional, Kim, Yong-Sung, additional, Angyal, Adrienn, additional, Kiss-Toth, Endre, additional, and Harteneck, Christian, additional

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2012
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38. TPD52 (Tumor Protein D52)

Author

Gonçalves, João, primary, Soares, Helena, additional, Eberhardt, Norman L., additional, Lummis, Sarah C. R., additional, Soto-Pantoja, David R., additional, Roberts, David D., additional, Maitra, Umadas, additional, Majumdar, Romit, additional, Biswas, Arunima, additional, Choudhuri, Avik, additional, Krishnan, Jayalakshmi, additional, Choi, Sangdun, additional, Atif, Shaikh M., additional, McSorley, Stephen J., additional, Greenwood, Michael T., additional, Butt, Aisha Qasim, additional, Miggin, Sinéad M., additional, Tuon, Felipe Francisco, additional, Shevlin, Enda, additional, Della-Franca, Austin, additional, Chen, Yuyan, additional, Byrne, Jennifer Anne, additional, Virla, Dimitra, additional, Tsatsanis, Christos, additional, Eliopoulos, Aristides G., additional, Landström, Maréne, additional, Sundar, Reshma, additional, Sung, Eun-Sil, additional, Kim, Yong-Sung, additional, Angyal, Adrienn, additional, Kiss-Toth, Endre, additional, and Harteneck, Christian, additional

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2012
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39. TEAD-3

Author

Gonçalves, João, primary, Soares, Helena, additional, Eberhardt, Norman L., additional, Lummis, Sarah C. R., additional, Soto-Pantoja, David R., additional, Roberts, David D., additional, Maitra, Umadas, additional, Majumdar, Romit, additional, Biswas, Arunima, additional, Choudhuri, Avik, additional, Krishnan, Jayalakshmi, additional, Choi, Sangdun, additional, Atif, Shaikh M., additional, McSorley, Stephen J., additional, Greenwood, Michael T., additional, Butt, Aisha Qasim, additional, Miggin, Sinéad M., additional, Tuon, Felipe Francisco, additional, Shevlin, Enda, additional, Della-Franca, Austin, additional, Chen, Yuyan, additional, Byrne, Jennifer Anne, additional, Virla, Dimitra, additional, Tsatsanis, Christos, additional, Eliopoulos, Aristides G., additional, Landström, Maréne, additional, Sundar, Reshma, additional, Sung, Eun-Sil, additional, Kim, Yong-Sung, additional, Angyal, Adrienn, additional, Kiss-Toth, Endre, additional, and Harteneck, Christian, additional

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2012
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40. TICAM-1

Author

Gonçalves, João, primary, Soares, Helena, additional, Eberhardt, Norman L., additional, Lummis, Sarah C. R., additional, Soto-Pantoja, David R., additional, Roberts, David D., additional, Maitra, Umadas, additional, Majumdar, Romit, additional, Biswas, Arunima, additional, Choudhuri, Avik, additional, Krishnan, Jayalakshmi, additional, Choi, Sangdun, additional, Atif, Shaikh M., additional, McSorley, Stephen J., additional, Greenwood, Michael T., additional, Butt, Aisha Qasim, additional, Miggin, Sinéad M., additional, Tuon, Felipe Francisco, additional, Shevlin, Enda, additional, Della-Franca, Austin, additional, Chen, Yuyan, additional, Byrne, Jennifer Anne, additional, Virla, Dimitra, additional, Tsatsanis, Christos, additional, Eliopoulos, Aristides G., additional, Landström, Maréne, additional, Sundar, Reshma, additional, Sung, Eun-Sil, additional, Kim, Yong-Sung, additional, Angyal, Adrienn, additional, Kiss-Toth, Endre, additional, and Harteneck, Christian, additional

Published
2012
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41. Toll-like receptor 5

Author

Gonçalves, João, primary, Soares, Helena, additional, Eberhardt, Norman L., additional, Lummis, Sarah C. R., additional, Soto-Pantoja, David R., additional, Roberts, David D., additional, Maitra, Umadas, additional, Majumdar, Romit, additional, Biswas, Arunima, additional, Choudhuri, Avik, additional, Krishnan, Jayalakshmi, additional, Choi, Sangdun, additional, Atif, Shaikh M., additional, McSorley, Stephen J., additional, Greenwood, Michael T., additional, Butt, Aisha Qasim, additional, Miggin, Sinéad M., additional, Tuon, Felipe Francisco, additional, Shevlin, Enda, additional, Della-Franca, Austin, additional, Chen, Yuyan, additional, Byrne, Jennifer Anne, additional, Virla, Dimitra, additional, Tsatsanis, Christos, additional, Eliopoulos, Aristides G., additional, Landström, Maréne, additional, Sundar, Reshma, additional, Sung, Eun-Sil, additional, Kim, Yong-Sung, additional, Angyal, Adrienn, additional, Kiss-Toth, Endre, additional, and Harteneck, Christian, additional

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2012
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42. Type A Endothelin Receptor

Author

Gonçalves, João, primary, Soares, Helena, additional, Eberhardt, Norman L., additional, Lummis, Sarah C. R., additional, Soto-Pantoja, David R., additional, Roberts, David D., additional, Maitra, Umadas, additional, Majumdar, Romit, additional, Biswas, Arunima, additional, Choudhuri, Avik, additional, Krishnan, Jayalakshmi, additional, Choi, Sangdun, additional, Atif, Shaikh M., additional, McSorley, Stephen J., additional, Greenwood, Michael T., additional, Butt, Aisha Qasim, additional, Miggin, Sinéad M., additional, Tuon, Felipe Francisco, additional, Shevlin, Enda, additional, Della-Franca, Austin, additional, Chen, Yuyan, additional, Byrne, Jennifer Anne, additional, Virla, Dimitra, additional, Tsatsanis, Christos, additional, Eliopoulos, Aristides G., additional, Landström, Maréne, additional, Sundar, Reshma, additional, Sung, Eun-Sil, additional, Kim, Yong-Sung, additional, Angyal, Adrienn, additional, Kiss-Toth, Endre, additional, and Harteneck, Christian, additional

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2012
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43. TRIF-Related Adapter Molecule

Author

Gonçalves, João, primary, Soares, Helena, additional, Eberhardt, Norman L., additional, Lummis, Sarah C. R., additional, Soto-Pantoja, David R., additional, Roberts, David D., additional, Maitra, Umadas, additional, Majumdar, Romit, additional, Biswas, Arunima, additional, Choudhuri, Avik, additional, Krishnan, Jayalakshmi, additional, Choi, Sangdun, additional, Atif, Shaikh M., additional, McSorley, Stephen J., additional, Greenwood, Michael T., additional, Butt, Aisha Qasim, additional, Miggin, Sinéad M., additional, Tuon, Felipe Francisco, additional, Shevlin, Enda, additional, Della-Franca, Austin, additional, Chen, Yuyan, additional, Byrne, Jennifer Anne, additional, Virla, Dimitra, additional, Tsatsanis, Christos, additional, Eliopoulos, Aristides G., additional, Landström, Maréne, additional, Sundar, Reshma, additional, Sung, Eun-Sil, additional, Kim, Yong-Sung, additional, Angyal, Adrienn, additional, Kiss-Toth, Endre, additional, and Harteneck, Christian, additional

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2012
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44. tm-PTPe

Author

Gonçalves, João, primary, Soares, Helena, additional, Eberhardt, Norman L., additional, Lummis, Sarah C. R., additional, Soto-Pantoja, David R., additional, Roberts, David D., additional, Maitra, Umadas, additional, Majumdar, Romit, additional, Biswas, Arunima, additional, Choudhuri, Avik, additional, Krishnan, Jayalakshmi, additional, Choi, Sangdun, additional, Atif, Shaikh M., additional, McSorley, Stephen J., additional, Greenwood, Michael T., additional, Butt, Aisha Qasim, additional, Miggin, Sinéad M., additional, Tuon, Felipe Francisco, additional, Shevlin, Enda, additional, Della-Franca, Austin, additional, Chen, Yuyan, additional, Byrne, Jennifer Anne, additional, Virla, Dimitra, additional, Tsatsanis, Christos, additional, Eliopoulos, Aristides G., additional, Landström, Maréne, additional, Sundar, Reshma, additional, Sung, Eun-Sil, additional, Kim, Yong-Sung, additional, Angyal, Adrienn, additional, Kiss-Toth, Endre, additional, and Harteneck, Christian, additional

Published
2012
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45. TIR-Domain-Containing Adapter Protein Inducing IFN-Beta

Author

Gonçalves, João, primary, Soares, Helena, additional, Eberhardt, Norman L., additional, Lummis, Sarah C. R., additional, Soto-Pantoja, David R., additional, Roberts, David D., additional, Maitra, Umadas, additional, Majumdar, Romit, additional, Biswas, Arunima, additional, Choudhuri, Avik, additional, Krishnan, Jayalakshmi, additional, Choi, Sangdun, additional, Atif, Shaikh M., additional, McSorley, Stephen J., additional, Greenwood, Michael T., additional, Butt, Aisha Qasim, additional, Miggin, Sinéad M., additional, Tuon, Felipe Francisco, additional, Shevlin, Enda, additional, Della-Franca, Austin, additional, Chen, Yuyan, additional, Byrne, Jennifer Anne, additional, Virla, Dimitra, additional, Tsatsanis, Christos, additional, Eliopoulos, Aristides G., additional, Landström, Maréne, additional, Sundar, Reshma, additional, Sung, Eun-Sil, additional, Kim, Yong-Sung, additional, Angyal, Adrienn, additional, Kiss-Toth, Endre, additional, and Harteneck, Christian, additional

Published
2012
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46. TIR-Domain-Containing Adapter Molecule 2

Author

Gonçalves, João, primary, Soares, Helena, additional, Eberhardt, Norman L., additional, Lummis, Sarah C. R., additional, Soto-Pantoja, David R., additional, Roberts, David D., additional, Maitra, Umadas, additional, Majumdar, Romit, additional, Biswas, Arunima, additional, Choudhuri, Avik, additional, Krishnan, Jayalakshmi, additional, Choi, Sangdun, additional, Atif, Shaikh M., additional, McSorley, Stephen J., additional, Greenwood, Michael T., additional, Butt, Aisha Qasim, additional, Miggin, Sinéad M., additional, Tuon, Felipe Francisco, additional, Shevlin, Enda, additional, Della-Franca, Austin, additional, Chen, Yuyan, additional, Byrne, Jennifer Anne, additional, Virla, Dimitra, additional, Tsatsanis, Christos, additional, Eliopoulos, Aristides G., additional, Landström, Maréne, additional, Sundar, Reshma, additional, Sung, Eun-Sil, additional, Kim, Yong-Sung, additional, Angyal, Adrienn, additional, Kiss-Toth, Endre, additional, and Harteneck, Christian, additional

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2012
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47. TSPAN 28

Author

Gonçalves, João, primary, Soares, Helena, additional, Eberhardt, Norman L., additional, Lummis, Sarah C. R., additional, Soto-Pantoja, David R., additional, Roberts, David D., additional, Maitra, Umadas, additional, Majumdar, Romit, additional, Biswas, Arunima, additional, Choudhuri, Avik, additional, Krishnan, Jayalakshmi, additional, Choi, Sangdun, additional, Atif, Shaikh M., additional, McSorley, Stephen J., additional, Greenwood, Michael T., additional, Butt, Aisha Qasim, additional, Miggin, Sinéad M., additional, Tuon, Felipe Francisco, additional, Shevlin, Enda, additional, Della-Franca, Austin, additional, Chen, Yuyan, additional, Byrne, Jennifer Anne, additional, Virla, Dimitra, additional, Tsatsanis, Christos, additional, Eliopoulos, Aristides G., additional, Landström, Maréne, additional, Sundar, Reshma, additional, Sung, Eun-Sil, additional, Kim, Yong-Sung, additional, Angyal, Adrienn, additional, Kiss-Toth, Endre, additional, and Harteneck, Christian, additional

Published
2012
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48. Toll-Like Receptor Adaptor Protein 3

Author

Gonçalves, João, primary, Soares, Helena, additional, Eberhardt, Norman L., additional, Lummis, Sarah C. R., additional, Soto-Pantoja, David R., additional, Roberts, David D., additional, Maitra, Umadas, additional, Majumdar, Romit, additional, Biswas, Arunima, additional, Choudhuri, Avik, additional, Krishnan, Jayalakshmi, additional, Choi, Sangdun, additional, Atif, Shaikh M., additional, McSorley, Stephen J., additional, Greenwood, Michael T., additional, Butt, Aisha Qasim, additional, Miggin, Sinéad M., additional, Tuon, Felipe Francisco, additional, Shevlin, Enda, additional, Della-Franca, Austin, additional, Chen, Yuyan, additional, Byrne, Jennifer Anne, additional, Virla, Dimitra, additional, Tsatsanis, Christos, additional, Eliopoulos, Aristides G., additional, Landström, Maréne, additional, Sundar, Reshma, additional, Sung, Eun-Sil, additional, Kim, Yong-Sung, additional, Angyal, Adrienn, additional, Kiss-Toth, Endre, additional, and Harteneck, Christian, additional

Published
2012
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49. Toll-Like Receptor 4 Adapter Protein

Author

Gonçalves, João, primary, Soares, Helena, additional, Eberhardt, Norman L., additional, Lummis, Sarah C. R., additional, Soto-Pantoja, David R., additional, Roberts, David D., additional, Maitra, Umadas, additional, Majumdar, Romit, additional, Biswas, Arunima, additional, Choudhuri, Avik, additional, Krishnan, Jayalakshmi, additional, Choi, Sangdun, additional, Atif, Shaikh M., additional, McSorley, Stephen J., additional, Greenwood, Michael T., additional, Butt, Aisha Qasim, additional, Miggin, Sinéad M., additional, Tuon, Felipe Francisco, additional, Shevlin, Enda, additional, Della-Franca, Austin, additional, Chen, Yuyan, additional, Byrne, Jennifer Anne, additional, Virla, Dimitra, additional, Tsatsanis, Christos, additional, Eliopoulos, Aristides G., additional, Landström, Maréne, additional, Sundar, Reshma, additional, Sung, Eun-Sil, additional, Kim, Yong-Sung, additional, Angyal, Adrienn, additional, Kiss-Toth, Endre, additional, and Harteneck, Christian, additional

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2012
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50. Type II Interferon

Author

Gonçalves, João, primary, Soares, Helena, additional, Eberhardt, Norman L., additional, Lummis, Sarah C. R., additional, Soto-Pantoja, David R., additional, Roberts, David D., additional, Maitra, Umadas, additional, Majumdar, Romit, additional, Biswas, Arunima, additional, Choudhuri, Avik, additional, Krishnan, Jayalakshmi, additional, Choi, Sangdun, additional, Atif, Shaikh M., additional, McSorley, Stephen J., additional, Greenwood, Michael T., additional, Butt, Aisha Qasim, additional, Miggin, Sinéad M., additional, Tuon, Felipe Francisco, additional, Shevlin, Enda, additional, Della-Franca, Austin, additional, Chen, Yuyan, additional, Byrne, Jennifer Anne, additional, Virla, Dimitra, additional, Tsatsanis, Christos, additional, Eliopoulos, Aristides G., additional, Landström, Maréne, additional, Sundar, Reshma, additional, Sung, Eun-Sil, additional, Kim, Yong-Sung, additional, Angyal, Adrienn, additional, Kiss-Toth, Endre, additional, and Harteneck, Christian, additional

Published
2012
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