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2,396 results on '"Niebel A"'

1. Fundamental solutions to Kolmogorov-Fokker-Planck equations with rough coefficients: existence, uniqueness, upper estimates

Author

Auscher, Pascal, Imbert, Cyril, and Niebel, Lukas

Subjects
Mathematics - Analysis of PDEs
Abstract

We show the existence and uniqueness of fundamental solution operators to Kolmo\-gorov-Fokker-Planck equations with rough (measurable) coefficients and local or integral diffusion on finite and infinite time strips. In the local case, that is to say when the diffusion operator is of differential type, we prove $\L^2$ decay using Davies' method and the conservation property. We also prove that the existence of a generalized fundamental solution with the expected pointwise Gaussian upper bound is equivalent to Moser's $\L^2-\L^\infty$ estimates for local weak solutions to the equation and its adjoint. When coefficients are real, this gives the existence and uniqueness of such a generalized fundamental solution and a new and natural way to obtain pointwise decay., Comment: 26 pages, submitted, minor corrections of typos

Published
2024

2. Weak solutions to Kolmogorov-Fokker-Planck equations: regularity, existence and uniqueness

Author

Auscher, Pascal, Imbert, Cyril, and Niebel, Lukas

Subjects
Mathematics - Analysis of PDEs
Abstract

In this article, we establish embeddings {\`a} la Lions and transfer of regularity {\`a} la Bouchut for a large scale of kinetic spaces. We use them to identify a notion of weak solutions to Kolmogorov-Fokker-Planck equations with (local or integral) diffusion and rough (measurable) coefficients under minimal requirements. We prove their existence and uniqueness for a large class of source terms, first in full space for the time, position and velocity variables and then for the kinetic Cauchy problem on infinite and finite time intervals., Comment: 40 pages, submitted. A correction to the argument in Theorem 6.7 and the corresponding argument in Section 7. Statements unchanged. Some typos eliminated

Published
2024

7. A trajectorial interpretation of Moser's proof of the Harnack inequality

Author

Niebel, Lukas and Zacher, Rico

Subjects
Mathematics - Analysis of PDEs, 35K10, 35B45, 35B65, 35J15
Abstract

In 1971 Moser published a simplified version of his proof of the parabolic Harnack inequality. The core new ingredient is a fundamental lemma due to Bombieri and Giusti, which combines an $L^p-L^\infty$-estimate with a weak $L^1$-estimate for the logarithm of supersolutions. In this note, we give a novel proof of this weak $L^1$-estimate. The presented argument uses parabolic trajectories and does not use any Poincar\'e inequality. Moreover, the proposed argument gives a geometric interpretation of Moser's result and could allow transferring Moser's method to other equations.

Published
2022

8. On a kinetic Poincar\'e inequality and beyond

Author

Niebel, Lukas and Zacher, Rico

Subjects
Mathematics - Analysis of PDEs, 35K70, 26D10, 35B45, 35B65, 35H10
Abstract

In this article, we give a trajectorial proof of a kinetic Poincar\'e inequality which plays an important role in the De Giorgi-Nash-Moser theory for kinetic equations. The present work improves a result due to J. Guerand and C. Mouhot [10] in several directions. We use kinetic trajectories along the vector fields $\partial_t + v \cdot \nabla_x$ and $\partial_{v_i}$, $i = 1,\dots, d$ and do not rely on higher-order commutators such as $[\partial_{v_i},\partial_t + v \cdot \nabla_x] = \partial_{x_i}$ or on the fundamental solution. The presented method also applies to more general hypoelliptic equations. We illustrate this by studying a Kolmogorov equation with $k$ steps., Comment: We added more explanations and references. Comments are welcome

Published
2022

9. Targeted protein degradation through site-specific antibody conjugation with mannose 6-phosphate glycan

Author

Kaori Mukai, Robert Cost, Xin Sheen Zhang, Emily Condiff, Joanne Cotton, Xiaohua Liu, Ekaterina Boudanova, Björn Niebel, Peter Piepenhagen, Xinming Cai, Anna Park, and Qun Zhou

Subjects
bisM6P-conjugated antibody, CI-MPR, LYTAC, M6P, protein degradation, Therapeutics. Pharmacology, RM1-950, Immunologic diseases. Allergy, RC581-607
Abstract

Recent developments in targeted protein degradation have provided great opportunities to eliminating extracellular protein targets using potential therapies with unique mechanisms of action and pharmacology. Among them, Lysosome-Targeting Chimeras (LYTACs) acting through mannose 6-phosphate receptor (M6PR) have been shown to facilitate degradation of several soluble and membrane-associated proteins in lysosomes with high efficiency. Herein we have developed a novel site-specific antibody conjugation approach to generate antibody mannose 6-phosphate (M6P) conjugates. The method uses a high affinity synthetic M6P glycan, bisM6P, that is coupled to an Fc-engineered antibody NNAS. This mutant without any effector function was generated by switching the native glycosylation site from position 297 to 298 converting non-sialylated structures to highly sialylated N-glycans. The sialic acid of the glycans attached to Asn298 in the engineered antibody was selectively conjugated to bisM6P without chemoenzymatic modification, which is often used for site-specific antibody conjugation through glycans. The conjugate is mainly homogeneous by analysis using mass spectrometry, typically with one or two glycans coupled. The M6P-conjugated antibody against a protein of interest (POI) efficiently internalized targeted soluble proteins, such as human tumor necrosis factor (TNF), in both cancer cell lines and human immune cells, through the endo-lysosomal pathway as demonstrated by confocal microscopy and flow cytometry. TNF in cell culture media was significantly depleted after the cells were incubated with the M6P-conjugated antibody. TNF internalization is mediated through M6PR, and it is correlated well with cell surface expression of cation-independent M6PR (CI-MPR) in immune cells. A significant amount of CI-MPR remains on the cell surface, while internalized TNF is degraded in lysosomes. Thus, the antibody-M6P conjugate is highly efficient in inducing internalization and subsequent lysosome-mediated protein degradation. Our platform provides a unique method for producing biologics-based degraders that may be used to treat diseases through event-driven pharmacology, thereby addressing unmet medical needs.

Published
2024
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12. Hepatitis C virus diversity and treatment outcomes in Benin: a prospective cohort study

Author

Ahovègbé, Lucrèce, Shah, Rajiv, Kpossou, Aboudou Raïmi, Davis, Chris, Niebel, Marc, Filipe, Ana, Goldstein, Emily, Alassan, Khadidjatou S, Keke, René, Sehonou, Jean, Kodjoh, Nicolas, Gbedo, Sossa Edmond, Ray, Surajit, Wilkie, Craig, Vattipally, Sreenu, Tong, Lily, Kamba, Pakoyo F, Gbenoudon, S Judith, Gunson, Rory, Ogwang, Patrick, and Thomson, Emma C

Published
2024
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13. The non-destructive investigation of a late antique knob bow fibula (Bügelknopffibel) from Kaiseraugst/CH using Muon Induced X-ray Emission (MIXE)

Author

Biswas, Sayani, Megatli-Niebel, Isabel, Raselli, Lilian, Simke, Ronald, Cocolios, Thomas Elias, Deokar, Nilesh, Elender, Matthias, Gerchow, Lars, Hess, Herbert, Khasanov, Rustem, Knecht, Andreas, Luetkens, Hubertus, Ninomiya, Kazuhiko, Papa, Angela, Prokscha, Thomas, Reiter, Peter, Sato, Akira, Severijns, Nathal, Shiroka, Toni, Seidlitz, Michael, Vogiatzi, Stergiani Marina, Wang, Chennan, Wauters, Frederik, Warr, Nigel, and Amato, Alex

Published
2023
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16. Hereditary epidermolytic palmoplantar keratosis due to a novel desmoglein‐1 mutation: A case report

Author

Kevin Koschitzki, Bernadett Kurz, Julia Schreml, Judith Fischer, Alrun Hotz, Christoph M. Hammers, Mark Berneburg, Dennis Niebel, and Stephan Schreml

Subjects
disorders of cornification, desmoglein‐1, keratoderma, palmoplantar, Medicine, Medicine (General), R5-920
Abstract

Key Clinical Message Keratosis palmoplantaris striata type I (SPPK‐I) is a rare autosomal‐dominant type of hereditary epidermolytic palmoplantar keratoderma, which can be caused by mutations in desmoglein‐1 (DSG‐1). Patients suffer from hyperkeratotic plaques and painful palmoplantar fissures. Unfortunately, treatment options including salicylic vaseline, topical corticosteroids, phototherapy, and retinoids are inefficient. Abstract Hereditary palmoplantar keratodermas (PPKs) represent a heterogeneous group of rare skin disorders with epidermal palmoplantar hyperkeratosis. Mutations in the desmoglein 1 gene (DSG1), a transmembrane glycoprotein, have been reported primarily in striate PPKs. We report a patient with keratosis palmoplantaris striata type I (SPPK‐I) with a specific pathogenic variant [c.349C>T, p.(Arg117*)] in DSG1. Despite increased understanding, effective treatment options for PPK, including SPPK‐I, remain limited.

Published
2024
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19. Viruses associated with measles-like illnesses in Uganda

Author

Namuwulya, Prossy, Ashraf, Shirin, Niebel, Marc, Ssekagiri, Alfred, Tushabe, Phionah, Kakooza, Proscovia, Tong, Lily, Bukenya, Henry, Jerome, Hanna, Davis, Chris, Birungi, Molly, Turyahabwe, Irene, Mugaga, Arnold, Eliku, James Peter, Francis, Aine, Nakabazzi, Lucy, Nsubuga, Fred, Katushabe, Edson, Kisakye, Annet, Ampeire, Immaculate, Nanteza, Ann, Kaleebu, Pontiano, Bakamutumaho, Barnabas, Nsamba, Peninah, Kazibwe, Anne, da Silva Filipe, Ana, Tweyongyere, Robert, Bwogi, Josephine, and Thomson, Emma C.

Published
2024
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21. Kinetic maximal $L^p_\mu(L^p)$-regularity for the fractional Kolmogorov equation with variable density

Author

Niebel, Lukas

Subjects
Mathematics - Analysis of PDEs, 35K59, 35K65, 45K05
Abstract

We consider the Kolmogorov equation, where the right-hand side is given by a non-local integro-differential operator comparable to the fractional Laplacian in velocity with possibly time, space and velocity dependent density. We prove that this equation admits kinetic maximal $L^p_\mu$-regularity under suitable assumptions on the density and on $p$ and $\mu$. We apply this result to prove short-time existence of strong $L^p_\mu$-solutions to quasilinear fractional kinetic partial differential equations., Comment: Added more explanations in Section 2. Changed parts of Section 4

Published
2021

22. Retrospective Single-Center Case Study of Clinical Variables and the Degree of Actinic Elastosis Associated with Rare Skin Cancers

Author

Konstantin Drexler, Lara Bollmann, Sigrid Karrer, Mark Berneburg, Sebastian Haferkamp, and Dennis Niebel

Subjects
atypical fibroxanthoma, pleomorphic dermal sarcoma, dermatofibrosarcoma protuberans, Merkel cell carcinoma, Kaposi sarcoma, leiomyosarcoma, Biology (General), QH301-705.5
Abstract

(1) Background: Rare skin cancers include epithelial, neuroendocrine, and hematopoietic neoplasias as well as cutaneous sarcomas. Ultraviolet (UV) radiation and sunburns are important drivers for the incidence of certain cutaneous sarcomas; however, the pathogenetic role of UV light is less clear in rare skin cancers compared to keratinocyte cancer and melanoma. In this study, we compared the degree of actinic elastosis (AE) as a surrogate for lifetime UV exposure among selected rare skin cancers (atypical fibroxanthoma [AFX], pleomorphic dermal sarcoma [PDS], dermatofibrosarcoma protuberans [DFSP], Kaposi sarcoma [KS], Merkel cell carcinoma [MCC], and leiomyosarcoma [LMS]) while taking into account relevant clinical variables (age, sex, and body site). (2) Methods: We newly established a semi-quantitative score for the degree of AE ranging from 0 = none to 3 = total loss of elastic fibers (basophilic degeneration) and multiplied it by the perilesional vertical extent (depth), measured histometrically (tumor-associated elastosis grade (TEG)). We matched the TEG of n = 210 rare skin cancers from 210 patients with their clinical variables. (3) Results: TEG values were correlated with age and whether tumors arose on UV-exposed body sites. TEG values were significantly higher in AFX and PDS cases compared to all other analyzed rare skin cancer types. As expected, TEG values were low in DFSP and KS, while MCC cases exhibited intermediate TEG values. (4) Conclusions: High cumulative UV exposure is more strongly associated with AFX/PDS and MCC than with other rare skin cancers. These important results expand the available data associated with rare skin cancers while also offering insight into the value of differentiating among these tumor types based on their relationship with sun exposure, potentially informing preventative, diagnostic and/or therapeutic approaches.

Published
2024
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23. Kinetic maximal $L^p$-regularity with temporal weights and application to quasilinear kinetic diffusion equations

Author

Niebel, Lukas and Zacher, Rico

Subjects
Mathematics - Analysis of PDEs, 35K65, 35B65, 35K59
Abstract

We introduce the concept of kinetic maximal $L^p$-regularity with temporal weights and prove that this property is satisfied for the (fractional) Kolmogorov equation. We show that solutions are continuous with values in the trace space and prove, in particular, that the trace space can be characterized in terms of anisotropic Besov spaces. We further extend the property of kinetic maximal $L^p_\mu$-regularity to the Kolmogorov equation with variable coefficients. Finally, we show how kinetic maximal $L^p_\mu$-regularity can be used to obtain local existence of solutions to a class of quasilinear kinetic equations and illustrate our result with a quasilinear kinetic diffusion equation.

Published
2020

27. Kinetic maximal $L^2$-regularity for the (fractional) Kolmogorov equation

Author

Niebel, Lukas and Zacher, Rico

Subjects
Mathematics - Analysis of PDEs, 35K65, 35B65, 35H10
Abstract

We introduce the notion of kinetic maximal $L^2$-regularity with temporal weights for the (fractional) Kolmogorov equation. In particular, we determine the function spaces for the inhomogeneity and the initial value which characterize the regularity of solutions to the fractional Kolmogorov equation in terms of fractional anisotropic Sobolev spaces. It is shown that solutions of the homogeneous (fractional) Kolmogorov equation define a semi-flow in a suitable function space and the property of instantaneous regularization is investigated., Comment: 23 pages

Published
2020

28. The non-destructive investigation of a late antique knob bow fibula (Bügelknopffibel) from Kaiseraugst/CH using Muon Induced X-ray Emission (MIXE)

Author

Sayani Biswas, Isabel Megatli-Niebel, Lilian Raselli, Ronald Simke, Thomas Elias Cocolios, Nilesh Deokar, Matthias Elender, Lars Gerchow, Herbert Hess, Rustem Khasanov, Andreas Knecht, Hubertus Luetkens, Kazuhiko Ninomiya, Angela Papa, Thomas Prokscha, Peter Reiter, Akira Sato, Nathal Severijns, Toni Shiroka, Michael Seidlitz, Stergiani Marina Vogiatzi, Chennan Wang, Frederik Wauters, Nigel Warr, and Alex Amato

Subjects
Knob bow fibula (Leutkirch type), Copper alloy, Muon Induced X-ray Emission (MIXE), Non-destructive elemental analysis, Depth-resolved, Fine Arts, Analytical chemistry, QD71-142
Abstract

Abstract A knob bow fibula (Bügelknopffibel) of the Leutkirch type, which typologically belongs to the second half of the 4th and early 5th century CE, was excavated in 2018 in the Roman city of Augusta Raurica, present-day Kaiseraugst (AG, Switzerland). This was analyzed for the first time for its elemental composition by using the non-destructive technique of Muon Induced X-ray Emission (MIXE) in the continuous muon beam facility at the Paul Scherrer Institute (PSI). In the present work, the detection limit is 0.4 wt% with $$\sim$$ ∼ 1.5 hours of measurement time. The fibula was measured at six different positions, at a depth of 0.3–0.4 mm inside the material. The experimental results show that the fibula is made of bronze, containing the main elements copper (Cu), zinc (Zn), tin (Sn) and lead (Pb). The compositional similarities/differences between different parts of the fibula reveal that it was manufactured as two “workpieces”. One workpiece consists of the knob (13.0±0.6 wt% Pb), bow (11.9±0.4 wt% Pb) and foot (12.5 ± 0.9 wt% Pb). These show a higher Pb content, suggesting a cast bronze. The spiral (3.2 ± 0.2 wt% Pb), which is part of the other workpiece, has a comparatively lower Pb content, suggesting a forged bronze.

Published
2023
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32. Prevalence of Crimean-Congo haemorrhagic fever in livestock following a confirmed human case in Lyantonde district, Uganda

Author

Stella A. Atim, Marc Niebel, Shirin Ashraf, Patrick Vudriko, Steven Odongo, Stephen Balinandi, Peace Aber, Ronald Bameka, Anna R. Ademun, Charles Masembe, Robert Tweyongyere, and Emma C. Thomson

Subjects
Crimean-Congo haemorrhagic fever virus, CCHF antibodies, Tick-borne viral infections, CCHF outbreak, Livestock, Animals, Infectious and parasitic diseases, RC109-216
Abstract

Abstract Background Crimean-Congo haemorrhagic fever (CCHF) is a tick-borne viral infection, characterized by haemorrhagic fever in humans and transient asymptomatic infection in animals. It is an emerging human health threat causing sporadic outbreaks in Uganda. We conducted a detailed outbreak investigation in the animal population following the death from CCHF of a 42-year-old male cattle trader in Lyantonde district, Uganda. This was to ascertain the extent of CCHF virus (CCHFV) circulation among cattle and goats and to identify affected farms and ongoing increased environmental risk for future human infections. Methods We collected blood and tick samples from 117 cattle and 93 goats, and tested these for anti-CCHFV antibodies and antigen using an enzyme-linked immunosorbent assay (ELISA), quantitative reverse transcriptase polymerase chain reaction (qRT-PCR) and target enrichment next generation sequencing. Results CCHFV-specific IgG antibodies were detected in 110/117 (94.0%) cattle and 83/93 (89.3%) goats. Animal seropositivity was independently associated with female animals (AOR = 9.42, P = 0.002), and animals reared under a pastoral animal production system (AOR = 6.02, P = 0.019] were more likely to be seropositive than tethered or communally grazed animals. CCHFV was detected by sequencing in Rhipicephalus appendiculatus ticks but not in domestic animals. Conclusion This investigation demonstrated very high seroprevalence of CCHFV antibodies in both cattle and goats in farms associated with a human case of CCHF in Lyantonde. Therefore, building surveillance programs for CCHF around farms in this area and the Ugandan cattle corridor is indicated, in order to identify opportunities for case prevention and control. Graphical Abstract

Published
2023
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36. Indurated erythema of abdominal skin: An unusual presentation of metastatic endometrial carcinoma—Case report with literature review

Author

Dennis Niebel, Paula Kranert, Mark Berneburg, Konstantin Drexler, Maria Isabel vonEichborn, Jan Braess, Michael Allgäuer, and Sigrid Karrer

Subjects
Dermatology, RL1-803
Abstract

Abstract Carcinoma erysipelatoides (CE) is a rare clinical manifestation of cutaneous metastasis, which mimics inflammatory conditions such as erysipelas. Depending on the site of the originating tumour, unusual manifestations involving different sites of the body may occur. We herein report a case of a 60‐year‐old female patient with metastatic endometrial carcinoma presenting as CE of the abdominal skin and the inguinal folds. Even though the diagnosis of advanced malignancy had been established before and she was currently receiving chemotherapy (carboplatin and paclitaxel), the clinical appearance closely resembled fungal (candidal intertrigo) and consecutively bacterial (erysipelas) infection, which resulted in treatment with antimycotics and antibiotics at first. Dermatohistopathological examination of skin biopsies revealed a diffuse and nodular infiltrate of pleomorphic atypical tumour cells with strong expression of cytokeratin 7 and PAX8, also detectable within lymphatic vessels. Therapy comprised antiseptic ointments to prevent superinfection, palliative electron beam radiation and supportive care. Since there were no targetable KRAS‐, NRAS‐ and BRAF‐gene mutations, systemic therapy was switched to checkpoint inhibition (pembrolizumab) in combination with lenvatinib. The overall prognosis of cutaneous metastasis of endometrial carcinoma is dismal with most patients succumbing to disease within few months. Similarly, our patient died after 3 months due to sepsis in the course of malignant pleural effusion. We aim to highlight the possibility of unusual sites of CE and the risk of respective clinical misdiagnoses.

Published
2023
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39. DNA methylation regulates TIGIT expression within the melanoma microenvironment, is prognostic for overall survival, and predicts progression-free survival in patients treated with anti-PD-1 immunotherapy

Author

Niebel, Dennis, Fröhlich, Anne, Zarbl, Romina, Fietz, Simon, de Vos, Luka, Vogt, Timo J., Dietrich, Jörn, Sirokay, Judith, Kuster, Pia, Saavedra, Gonzalo, Ramírez Valladolid, Susana, Hoffmann, Friederike, Strieth, Sebastian, Landsberg, Jennifer, and Dietrich, Dimo

Published
2022
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40. Bullous Pemphigoid in Patients Receiving Immune-Checkpoint Inhibitors and Psoriatic Patients—Focus on Clinical and Histopathological Variation

Author

Dennis Niebel, Dagmar Wilsmann-Theis, Thomas Bieber, Mark Berneburg, Joerg Wenzel, and Christine Braegelmann

Subjects
pemphigoid, bullous, skin diseases, vesiculobullous, psoriasis, programmed cell death 1 receptor, Dermatology, RL1-803
Abstract

Background: The most common autoimmune blistering disease, bullous pemphigoid (BP), shows an increased prevalence in psoriatic patients and oncologic patients undergoing immune-checkpoint blockade (ICB). Even though the same autoantigens (BP180/BP230) are detectable, it remains obscure whether clinical or histopathological differences exist between these different groups of BP patients. In this study, we strived to analyze this matter based on own data and previously published reports. Methods: We performed an institutional chart review from 2010–2020 to identify BP patients with psoriasis (n = 6) or underlying ICB (n = 4) and matched them with idiopathic cases of BP (n = 33). We compared clinical characteristics, subtypes, and dermatopathological determinants (e.g., tissue eosinophilia/neutrophilia, papillary edema, lymphocytic infiltration) among the groups. Results: ICB-associated BP affects men more often and might show mucosal involvement more frequently. We found no statistically significant dermatopathological differences among the groups. Conclusions: Clinicians should be aware of an increased risk of BP in patients with psoriasis and oncologic patients receiving ICB; atypical pruritic skin lesions should prompt a workup including a skin biopsy for histopathology and direct immunofluorescence in these patients. Larger studies might be necessary to detect slight dermatopathological variation.

Published
2022
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42. Die Zukunftsquote: ein neuer Kompass für den Bundeshaushalt.

Author

Bohne, Albrecht, Heinemann, Friedrich, Niebel, Thomas, and Thöne, Michael

Subjects
DEBT, REFORMS
Abstract

Copyright of Perspektiven der Wirtschaftspolitik is the property of De Gruyter and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Published
2024
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45. Hospital admission and emergency care attendance risk for SARS-CoV-2 delta (B.1.617.2) compared with alpha (B.1.1.7) variants of concern: a cohort study

Author

Koshy, Cherian, Ash, Amy, Wise, Emma, Moore, Nathan, Mori, Matilde, Cortes, Nick, Lynch, Jessica, Kidd, Stephen, Fairley, Derek, Curran, Tanya, McKenna, James, Adams, Helen, Fraser, Christophe, Golubchik, Tanya, Bonsall, David, Hassan-Ibrahim, Mohammed, Malone, Cassandra, Cogger, Benjamin, Wantoch, Michelle, Reynolds, Nicola, Warne, Ben, Maksimovic, Joshua, Spellman, Karla, McCluggage, Kathryn, John, Michaela, Beer, Robert, Afifi, Safiah, Morgan, Sian, Marchbank, Angela, Price, Anna, Kitchen, Christine, Gulliver, Huw, Merrick, Ian, Southgate, Joel, Guest, Martyn, Munn, Robert, Workman, Trudy, Connor, Thomas, Fuller, William, Bresner, Catherine, Snell, Luke, Patel, Amita, Charalampous, Themoula, Nebbia, Gaia, Batra, Rahul, Edgeworth, Jonathan, Robson, Samuel, Beckett, Angela, Aanensen, David, Underwood, Anthony, Yeats, Corin, Abudahab, Khalil, Taylor, Ben, Menegazzo, Mirko, Clark, Gemma, Smith, Wendy, Khakh, Manjinder, Fleming, Vicki, Lister, Michelle, Howson-Wells, Hannah, Berry, Louise, Boswell, Tim, Joseph, Amelia, Willingham, Iona, Jones, Carl, Holmes, Christopher, Bird, Paul, Helmer, Thomas, Fallon, Karlie, Tang, Julian, Raviprakash, Veena, Campbell, Sharon, Sheriff, Nicola, Blakey, Victoria, Williams, Lesley-Anne, Loose, Matthew, Holmes, Nadine, Moore, Christopher, Carlile, Matthew, Wright, Victoria, Sang, Fei, Debebe, Johnny, Coll, Francesc, Signell, Adrian, Betancor, Gilberto, Wilson, Harry, Eldirdiri, Sahar, Kenyon, Anita, Davis, Thomas, Pybus, Oliver, du Plessis, Louis, Zarebski, Alex, Raghwani, Jayna, Kraemer, Moritz, Francois, Sarah, Attwood, Stephen, Vasylyeva, Tetyana, Escalera Zamudio, Marina, Gutierrez, Bernardo, Torok, M. Estee, Hamilton, William, Goodfellow, Ian, Hall, Grant, Jahun, Aminu, Chaudhry, Yasmin, Hosmillo, Myra, Pinckert, Malte, Georgana, Iliana, Moses, Samuel, Lowe, Hannah, Bedford, Luke, Moore, Jonathan, Stonehouse, Susanne, Fisher, Chloe, Awan, Ali, BoYes, John, Breuer, Judith, Harris, Kathryn, Brown, Julianne, Shah, Divya, Atkinson, Laura, Lee, Jack, Storey, Nathaniel, Flaviani, Flavia, Alcolea-Medina, Adela, Williams, Rebecca, Vernet, Gabrielle, Chapman, Michael, Levett, Lisa, Heaney, Judith, Chatterton, Wendy, Pusok, Monika, Xu-McCrae, Li, Smith, Darren, Bashton, Matthew, Young, Gregory, Holmes, Alison, Randell, Paul, Cox, Alison, Madona, Pinglawathee, Bolt, Frances, Price, James, Mookerjee, Siddharth, Ragonnet-Cronin, Manon, F. Nascimento, Fabricia, Jorgensen, David, Siveroni, Igor, Johnson, Rob, Boyd, Olivia, Geidelberg, Lily, Volz, Erik, Rowan, Aileen, Taylor, Graham, Smollett, Katherine, Loman, Nicholas, Quick, Joshua, McMurray, Claire, Stockton, Joanne, Nicholls, Sam, Rowe, Will, Poplawski, Radoslaw, McNally, Alan, Martinez Nunez, Rocio, Mason, Jenifer, Robinson, Trevor, O'Toole, Elaine, Watts, Joanne, Breen, Cassie, Cowell, Angela, Sluga, Graciela, Machin, Nicholas, Ahmad, Shazaad, George, Ryan, Halstead, Fenella, Sivaprakasam, Venkat, Hogsden, Wendy, Illingworth, Chris, Jackson, Chris, Thomson, Emma, Shepherd, James, Asamaphan, Patawee, Niebel, Marc, Li, Kathy, Shah, Rajiv, Jesudason, Natasha, Tong, Lily, Broos, Alice, Mair, Daniel, Nichols, Jenna, Carmichael, Stephen, Nomikou, Kyriaki, Aranday-Cortes, Elihu, Johnson, Natasha, Starinskij, Igor, da Silva Filipe, Ana, Robertson, David, Orton, Richard, Hughes, Joseph, Vattipally, Sreenu, Singer, Joshua, Nickbakhsh, Seema, Hale, Antony, Macfarlane-Smith, Louissa, Harper, Katherine, Carden, Holli, Taha, Yusri, Payne, Brendan, Burton-Fanning, Shirelle, Waugh, Sheila, Collins, Jennifer, Eltringham, Gary, Rushton, Steven, O'Brien, Sarah, Bradley, Amanda, Maclean, Alasdair, Mollett, Guy, Blacow, Rachel, Templeton, Kate, McHugh, Martin, Dewar, Rebecca, Wastenge, Elizabeth, Dervisevic, Samir, Stanley, Rachael, Meader, Emma, Coupland, Lindsay, Smith, Louise, Graham, Clive, Barton, Edward, Padgett, Debra, Scott, Garren, Swindells, Emma, Greenaway, Jane, Nelson, Andrew, McCann, Clare, Yew, Wen, Andersson, Monique, Peto, Timothy, Justice, Anita, Eyre, David, Crook, Derrick, Sloan, Tim, Duckworth, Nichola, Walsh, Sarah, Chauhan, Anoop, Glaysher, Sharon, Bicknell, Kelly, Wyllie, Sarah, Elliott, Scott, Lloyd, Allyson, Impey, Robert, Levene, Nick, Monaghan, Lynn, Bradley, Declan, Wyatt, Tim, Allara, Elias, Pearson, Clare, Osman, Husam, Bosworth, Andrew, Robinson, Esther, Muir, Peter, Vipond, Ian, Hopes, Richard, Pymont, Hannah, Hutchings, Stephanie, Curran, Martin, Parmar, Surendra, Lackenby, Angie, Mbisa, Tamyo, Platt, Steven, Miah, Shahjahan, Bibby, David, Manso, Carmen, Hubb, Jonathan, Chand, Meera, Dabrera, Gavin, Ramsay, Mary, Bradshaw, Daniel, Thornton, Alicia, Myers, Richard, Schaefer, Ulf, Groves, Natalie, Gallagher, Eileen, Lee, David, Williams, David, Ellaby, Nicholas, Harrison, Ian, Hartman, Hassan, Manesis, Nikos, Patel, Vineet, Bishop, Chloe, Chalker, Vicki, Ledesma, Juan, Twohig, Katherine, Holden, Matthew, Shaaban, Sharif, Birchley, Alec, Adams, Alexander, Davies, Alisha, Gaskin, Amy, Plimmer, Amy, Gatica-Wilcox, Bree, McKerr, Caoimhe, Moore, Catherine, Williams, Chris, Heyburn, David, De Lacy, Elen, Hilvers, Ember, Downing, Fatima, Shankar, Giri, Jones, Hannah, Asad, Hibo, Coombes, Jason, Watkins, Joanne, Evans, Johnathan, Fina, Laia, Gifford, Laura, Gilbert, Lauren, Graham, Lee, Perry, Malorie, Morgan, Mari, Bull, Matthew, Cronin, Michelle, Pacchiarini, Nicole, Craine, Noel, Jones, Rachel, Howe, Robin, Corden, 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Published
2022
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49. A lateral organ boundaries domain transcription factor acts downstream of the auxin response factor 2 to control nodulation and root architecture in Medicago truncatula

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Kirolinko, Cristina, primary, Hobecker, Karen, additional, Cueva, Marianela, additional, Botto, Florencia, additional, Christ, Aurélie, additional, Niebel, Andreas, additional, Ariel, Federico, additional, Blanco, Flavio Antonio, additional, Crespi, Martín, additional, and Zanetti, María Eugenia, additional

Published
2024
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