Search

Your search keyword '"Maglott"' showing total 668 results
Start Over Author "Maglott"
668 results on '"Maglott"'

51. Database resources of the National Center for Biotechnology Information.

Author

David L. Wheeler, Tanya Barrett, Dennis A. Benson, Stephen H. Bryant, Kathi Canese, Vyacheslav Chetvernin, Deanna M. Church, Michael DiCuccio, Ron Edgar, Scott Federhen, Michael Feolo, Lewis Y. Geer, Wolfgang Helmberg, Yuri Kapustin, Oleg Khovayko, David Landsman, David J. Lipman, Thomas L. Madden, Donna R. Maglott, Vadim Miller, James Ostell, Kim D. Pruitt, Gregory D. Schuler, Martin Shumway, Edwin Sequeira, Steven T. Sherry, Karl Sirotkin, Alexandre Souvorov, Grigory Starchenko, Roman L. Tatusov, Tatiana A. Tatusova, Lukas Wagner 0002, and Eugene Yaschenko

Published
2008
Full Text
View/download PDF

54. Database resources of the National Center for Biotechnology Information.

Author

David L. Wheeler, Tanya Barrett, Dennis A. Benson, Stephen H. Bryant, Kathi Canese, Vyacheslav Chetvernin, Deanna M. Church, Michael DiCuccio, Ron Edgar, Scott Federhen, Lewis Y. Geer, Yuri Kapustin, Oleg Khovayko, David Landsman, David J. Lipman, Thomas L. Madden, Donna R. Maglott, James Ostell, Vadim Miller, Kim D. Pruitt, Gregory D. Schuler, Edwin Sequeira, Steven T. Sherry, Karl Sirotkin, Alexandre Souvorov, Grigory Starchenko, Roman L. Tatusov, Tatiana A. Tatusova, Lukas Wagner 0002, and Eugene Yaschenko

Published
2007
Full Text
View/download PDF

55. The Human Variome Project

Author

Cotton, Richard G. H., Auerbach, Arleen D., Axton, Myles, Barash, Carol Isaacson, Berkovic, Samuel F., Brookes, Anthony J., Burn, John, Cutting, Garry, Dunnen, Johan T. den, Flicek, Paul, Freimer, Nelson, Greenblatt, Marc S., Howard, Heather J., Katz, Michael, Macrae, Finlay A., Maglott, Donna, Möslein, Gabriela, Povey, Sue, Ramesar, Rajkumar S., Richards, Carolyn S., Seminara, Daniela, Smith, Timothy D., Sobrido, María-Jesús, Solbakk, Jan Helge, Tanzi, Rudolph E., Tavtigian, Sean V., Taylor, Graham R., Utsunomiya, Joji, and Watson, Michael

Published
2008
Full Text
View/download PDF

56. Database resources of the National Center for Biotechnology Information.

Author

David L. Wheeler, Tanya Barrett, Dennis A. Benson, Stephen H. Bryant, Kathi Canese, Vyacheslav Chetvernin, Deanna M. Church, Michael DiCuccio, Ron Edgar, Scott Federhen, Lewis Y. Geer, Wolfgang Helmberg, Yuri Kapustin, David L. Kenton, Oleg Khovayko, David J. Lipman, Thomas L. Madden, Donna R. Maglott, James Ostell, Kim D. Pruitt, Gregory D. Schuler, Lynn M. Schriml, Edwin Sequeira, Stephen T. Sherry, Karl Sirotkin, Alexandre Souvorov, Grigory Starchenko, Tugba O. Suzek, Roman L. Tatusov, Tatiana A. Tatusova, Lukas Wagner 0002, and Eugene Yaschenko

Published
2006
Full Text
View/download PDF

57. eP369: Increased automation reduces turnaround time for submissions to ClinVar

Author

Landrum, Melissa, primary, Chitipiralla, Shanmuga, additional, Brown, Garth, additional, Chen, Chao, additional, Gu, Baoshan, additional, Hart, Jennifer, additional, Hoffman, Douglas, additional, Jang, Wonhee, additional, Liu, Chunlei, additional, Maddipatla, Zenith, additional, Maglott, Donna, additional, Maiti, Rama, additional, Mitchell, Joseph, additional, Rezaie, Tayebeh, additional, Riley, George, additional, Shao, David, additional, Zhou, George, additional, Lyoshin, Vitaly, additional, Swallow, Chris, additional, Kaur, Kuljeet, additional, Russette, Andrew, additional, and Kattman, Brandi, additional

Published
2022
Full Text
View/download PDF

60. Database resources of the National Center for Biotechnology Information.

Author

David L. Wheeler, Tanya Barrett, Dennis A. Benson, Stephen H. Bryant, Kathi Canese, Deanna M. Church, Michael DiCuccio, Ron Edgar, Scott Federhen, Wolfgang Helmberg, David L. Kenton, Oleg Khovayko, David J. Lipman, Thomas L. Madden, Donna R. Maglott, James Ostell, Joan U. Pontius, Kim D. Pruitt, Gregory D. Schuler, Lynn M. Schriml, Edwin Sequeira, Steven T. Sherry, Karl Sirotkin, Grigory Starchenko, Tugba O. Suzek, Roman L. Tatusov, Tatiana A. Tatusova, Lukas Wagner 0002, and Eugene Yaschenko

Published
2005
Full Text
View/download PDF

67. List of Contributors

Author

Abel, Haley, primary, Ajay, Shankar, additional, Al-Kateb, Hussam, additional, Amr, Sami S., additional, Bredemeyer, Andrew J., additional, Chang, Fengqi, additional, Chastain, Elizabeth C., additional, Church, Deanna M., additional, Cliften, Paul, additional, Cottrell, Catherine E., additional, Drury, Andrew, additional, Duncavage, Eric, additional, Funke, Birgit, additional, Gargis, Amy S., additional, Hagemann, Ian S., additional, Hambuch, Tina M., additional, Hegde, Madhuri R., additional, Hogue, Michelle, additional, Horner, Vanessa L., additional, Kalman, Lisa, additional, Ketkar, Shamika, additional, Klein, Roger D., additional, Kulkarni, Shashikant, additional, LaFramboise, William A., additional, Li, Marilyn M., additional, Liu, Cindy J., additional, Liu, Geoffrey L., additional, Lubin, Ira M., additional, Lyon, Elaine, additional, Maglott, Donna R., additional, Mao, Rong, additional, Mayfield, John, additional, Mead, Carri-Lyn, additional, Nagarajan, Rakesh, additional, Nikiforov, Yuri E., additional, Nikiforova, Marina N., additional, Nord, Alex, additional, O’Fallon, Brendan D., additional, Pfeifer, John, additional, Pritchard, Colin, additional, Ramos, Erica, additional, Rickhoff, Kris, additional, Roberts, Kristina A., additional, Rubinstein, Wendy S., additional, Salipante, Stephen J., additional, Salit, Marc, additional, Sehn, Jennifer K., additional, Solomon, Benjamin D., additional, Solomon, Stephanie, additional, Spencer, David H., additional, Zhang, Bin, additional, and Zook, Justin, additional

Published
2015
Full Text
View/download PDF

70. eP369: Increased automation reduces turnaround time for submissions to ClinVar

Author

Melissa Landrum, Shanmuga Chitipiralla, Garth Brown, Chao Chen, Baoshan Gu, Jennifer Hart, Douglas Hoffman, Wonhee Jang, Chunlei Liu, Zenith Maddipatla, Donna Maglott, Rama Maiti, Joseph Mitchell, Tayebeh Rezaie, George Riley, David Shao, George Zhou, Vitaly Lyoshin, Chris Swallow, Kuljeet Kaur, Andrew Russette, and Brandi Kattman

Subjects
Genetics (clinical)
Published
2022
Full Text
View/download PDF

71. ClinVar: improvements to accessing data

Author

Rama Maiti, Chao Chen, Douglas W. Hoffman, J. Bradley Holmes, Donna Maglott, Joseph Mitchell, Baoshan Gu, Garth Brown, Melissa J. Landrum, Brandi L. Kattman, Vitaly Lyoshin, Kuljeet Kaur, George Zhou, George R. Riley, Wonhee Jang, Jennifer Hart, Nuala A. O'Leary, Chunlei Liu, Valerie A. Schneider, Shanmuga Chitipiralla, Wenyao Shi, and Zenith Maddipatla

Subjects
Internet, 0303 health sciences, Information retrieval, National Library of Medicine (U.S.), Genome, Human, computer.internet_protocol, Summary data, Genetic variants, Genetic Variation, Genomics, Biology, United States, Search Engine, 03 medical and health sciences, 0302 clinical medicine, Haplotypes, Databases, Genetic, Genetics, Database Issue, Humans, Disease, computer, 030217 neurology & neurosurgery, XML, 030304 developmental biology
Abstract

ClinVar is a freely available, public archive of human genetic variants and interpretations of their relationships to diseases and other conditions, maintained at the National Institutes of Health (NIH). Submitted interpretations of variants are aggregated and made available on the ClinVar website (https://www.ncbi.nlm.nih.gov/clinvar/), and as downloadable files via FTP and through programmatic tools such as NCBI’s E-utilities. The default view on the ClinVar website, the Variation page, was recently redesigned. The new layout includes several new sections that make it easier to find submitted data as well as summary data such as all diseases and citations reported for the variant. The new design also better represents more complex data such as haplotypes and genotypes, as well as variants that are in ClinVar as part of a haplotype or genotype but have no interpretation for the single variant. ClinVar's variant-centric XML had its production release in April 2019. The ClinVar website and E-utilities both have been updated to support the VCV (variation in ClinVar) accession numbers found in the variant-centric XML file. ClinVar's search engine has been fine-tuned for improved retrieval of search results.

Published
2019
Full Text
View/download PDF

72. SPDI: data model for variants and applications at NCBI

Author

Donna Maglott, J. Bradley Holmes, Lon Phan, Eric Moyer, and Brandi L. Kattman

Subjects
Statistics and Probability, dbSNP, Computer science, Computational biology, Biochemistry, Set (abstract data type), 03 medical and health sciences, 0302 clinical medicine, Databases, Genetic, Subsequence, Genetic variation, RefSeq, Nucleotide, Allele, Molecular Biology, 030304 developmental biology, Sequence (medicine), chemistry.chemical_classification, 0303 health sciences, Genome, Genomics, Original Papers, Computer Science Applications, Computational Mathematics, Projection (relational algebra), Vocabulary, Controlled, Computational Theory and Mathematics, Data model, chemistry, Algorithms, 030217 neurology & neurosurgery, Function (biology), Reference genome
Abstract

MotivationNormalizing diverse representations of sequence variants is critical to the elucidation of the genetic basis of disease and biological function. NCBI has long wrestled with integrating data from multiple submitters to build databases such as dbSNP and ClinVar. Inconsistent representation of variants among variant callers, local databases, and tools results in discrepancies and duplications that complicate analysis. Current tools are not robust enough to manage variants in different formats and different reference sequence coordinates.ResultsThe SPDI (pronounced “speedy”) data model defines variants as a sequence of 4 operations: start at the boundary before the first position in the sequence S, advance P positions, delete D positions, then insert the sequence in the string I, giving the data model its name, SPDI. The SPDI model can thus be applied to both nucleotide and protein variants, but the services discussed here are limited to nucleotide. Current services convert representations between HGVS, VCF, and SPDI and provide two forms of normalization. The first, based on the NCBI Variant Overprecision Correction Algorithm, returns a unique, normalized representation termed the “Contextual Allele” for any input. The SPDI name, with its four operations, defines exactly the reference subsequence potentially affected by the variant, even in low complexity regions such as homopolymer and dinucleotide sequence repeats. The second level of normalization depends on an alignment dataset (ADS). SPDI services perform remapping (AKA lift-over) of variants from the input reference sequence to return a list of all equivalent Contextual Alleles based on the transcript or genomic sequences that were aligned. One of these contextual alleles is selected to represent all, usually that based on the latest genomic assembly such as GRCh38 and is designated as the unique “Canonical Allele”. ADS includes alignments between non-assembly RefSeq sequences (prefixed NM, NR, NG), as well inter- and intra-assembly-associated genomic sequences (NCs, NTs and NWs) and this allow for robust remapping and normalization of variants across sequences and assembly versions.Availability and implementationThe SPDI services are available for open access at: https://api.ncbi.nlm.nih.gov/variation/v0/Contactholmesbr@ncbi.nlm.nih.gov

Published
2019
Full Text
View/download PDF

75. Characterizing genetic variants for clinical action

Author

Ramos, Erin M., Din-Lovinescu, Corina, Berg, Jonathan S., Brooks, Lisa D., Duncanson, Audrey, Dunn, Michael, Good, Peter, Hubbard, Tim J.P., Jarvik, Gail P., OʼDonnell, Christopher, Sherry, Stephen T., Aronson, Naomi, Biesecker, Leslie G., Blumberg, Bruce, Calonge, Ned, Colhoun, Helen M., Epstein, Robert S., Flicek, Paul, Gordon, Erynn S., Green, Eric D., Green, Robert C., Hurles, Matthew, Kawamoto, Kensaku, Knaus, William, Ledbetter, David H., Levy, Howard P., Lyon, Elaine, Maglott, Donna, McLeod, Howard L., Rahman, Nazneen, Randhawa, Gurvaneet, Wicklund, Catherine, Manolio, Teri A., Chisholm, Rex L., and Williams, Marc S.

Published
2014
Full Text
View/download PDF

76. RefSeq: an update on mammalian reference sequences

Author

Pruitt, Kim D., Brown, Garth R., Hiatt, Susan M., Thibaud-Nissen, Françoise, Astashyn, Alexander, Ermolaeva, Olga, Farrell, Catherine M., Hart, Jennifer, Landrum, Melissa J., McGarvey, Kelly M., Murphy, Michael R., OʼLeary, Nuala A., Pujar, Shashikant, Rajput, Bhanu, Rangwala, Sanjida H., Riddick, Lillian D., Shkeda, Andrei, Sun, Hanzhen, Tamez, Pamela, Tully, Raymond E., Wallin, Craig, Webb, David, Weber, Janet, Wu, Wendy, DiCuccio, Michael, Kitts, Paul, Maglott, Donna R., Murphy, Terence D., and Ostell, James M.

Published
2014
Full Text
View/download PDF

81. Genes and Pathways Regulated by Androgens in Human Neural Cells, Potential Candidates for the Male Excess in Autism Spectrum Disorder

Author

Laure Chatrousse, Angélique Quartier, Jean-Louis Mandel, Stéphanie Le Gras, Céline Keime, Claire Redin, Anne Maglott-Roth, Laurent Brino, Amélie Piton, Alexandra Benchoua, and Nicolas Haumesser

Subjects
Male, 0301 basic medicine, Neurite, Autism Spectrum Disorder, Cell Survival, medicine.drug_class, Gene Expression, Biology, urologic and male genital diseases, Cell Line, 03 medical and health sciences, Sex Factors, 0302 clinical medicine, Neural Stem Cells, medicine, Humans, Cells, Cultured, Biological Psychiatry, Sequence Analysis, RNA, Cell Differentiation, Dihydrotestosterone, Androgen, Embryonic stem cell, Neural stem cell, Cell biology, Androgen receptor, 030104 developmental biology, Receptors, Androgen, Androgens, Female, Signal transduction, Chromatin immunoprecipitation, 030217 neurology & neurosurgery, medicine.drug
Abstract

Background Prenatal exposure to androgens during brain development in male individuals may participate to increase their susceptibility to develop neurodevelopmental disorders such as autism spectrum disorder (ASD) and intellectual disability. However, little is known about the action of androgens in human neural cells. Methods We used human neural stem cells differentiated from embryonic stem cells to investigate targets of androgens. Results RNA sequencing revealed that treatment with dihydrotestosterone (DHT) leads to subtle but significant changes in the expression of about 200 genes, encoding proteins of extracellular matrix or involved in signal transduction of growth factors (e.g., insulin/insulin growth factor 1). We showed that the most differentially expressed genes (DEGs), RGCC, RNF144B, NRCAM, TRIM22, FAM107A, IGFBP5, and LAMA2, are reproducibly regulated by different androgens in different genetic backgrounds. We showed, by overexpressing the androgen receptor in neuroblastoma cells SH-SY5Y or knocking it down in human neural stem cells, that this regulation involves the androgen receptor. A chromatin immunoprecipitation combined with direct sequencing analysis identified androgen receptor–bound sequences in nearly half of the DHT-DEGs and in numerous other genes. DHT-DEGs appear enriched in genes involved in ASD (ASXL3, NLGN4X, etc.), associated with ASD (NRCAM), or differentially expressed in patients with ASD (FAM107A, IGFBP5). Androgens increase human neural stem cell proliferation and survival in nutrient-deprived culture conditions, with no detectable effect on regulation of neurite outgrowth. Conclusions We characterized androgen action in neural progenitor cells, identifying DHT-DEGs that appear to be enriched in genes related to ASD. We also showed that androgens increase proliferation of neuronal precursors and protect them from death during their differentiation in nutrient-deprived conditions.

Published
2018
Full Text
View/download PDF

83. A study on the death of cell of sea urchins examines the proteins found in its genome

Author

Livingston, B.T., Killian, C.E., Wilt, F., Cameron, A., Landrum, M.J., Ermolaeva, O., Sapojnikov, V., Maglott, D.R., Buchanan, A.M., and Ettensohn, C.A.

Subjects
Sea urchins -- Genetic aspects, Biomineralization -- Analysis, Biological sciences
Abstract

A study on cellular mechanism of sea urchin examines its biomineralization process.

Published
2006

85. Lineage-specific biology revealed by a finished genome assembly of the mouse.

Author

Deanna M Church, Leo Goodstadt, Ladeana W Hillier, Michael C Zody, Steve Goldstein, Xinwe She, Carol J Bult, Richa Agarwala, Joshua L Cherry, Michael DiCuccio, Wratko Hlavina, Yuri Kapustin, Peter Meric, Donna Maglott, Zoë Birtle, Ana C Marques, Tina Graves, Shiguo Zhou, Brian Teague, Konstantinos Potamousis, Christopher Churas, Michael Place, Jill Herschleb, Ron Runnheim, Daniel Forrest, James Amos-Landgraf, David C Schwartz, Ze Cheng, Kerstin Lindblad-Toh, Evan E Eichler, Chris P Ponting, and Mouse Genome Sequencing Consortium

Subjects
Biology (General), QH301-705.5
Abstract

The mouse (Mus musculus) is the premier animal model for understanding human disease and development. Here we show that a comprehensive understanding of mouse biology is only possible with the availability of a finished, high-quality genome assembly. The finished clone-based assembly of the mouse strain C57BL/6J reported here has over 175,000 fewer gaps and over 139 Mb more of novel sequence, compared with the earlier MGSCv3 draft genome assembly. In a comprehensive analysis of this revised genome sequence, we are now able to define 20,210 protein-coding genes, over a thousand more than predicted in the human genome (19,042 genes). In addition, we identified 439 long, non-protein-coding RNAs with evidence for transcribed orthologs in human. We analyzed the complex and repetitive landscape of 267 Mb of sequence that was missing or misassembled in the previously published assembly, and we provide insights into the reasons for its resistance to sequencing and assembly by whole-genome shotgun approaches. Duplicated regions within newly assembled sequence tend to be of more recent ancestry than duplicates in the published draft, correcting our initial understanding of recent evolution on the mouse lineage. These duplicates appear to be largely composed of sequence regions containing transposable elements and duplicated protein-coding genes; of these, some may be fixed in the mouse population, but at least 40% of segmentally duplicated sequences are copy number variable even among laboratory mouse strains. Mouse lineage-specific regions contain 3,767 genes drawn mainly from rapidly-changing gene families associated with reproductive functions. The finished mouse genome assembly, therefore, greatly improves our understanding of rodent-specific biology and allows the delineation of ancestral biological functions that are shared with human from derived functions that are not.

Published
2009
Full Text
View/download PDF

86. Getting Ready for the Human Phenome Project: The 2012 Forum of the Human Variome Project

Author

Oetting, William S., Robinson, Peter N., Greenblatt, Marc S., Cotton, Richard G., Beck, Tim, Carey, John C., Doelken, Sandra C., Girdea, Marta, Groza, Tudor, Hamilton, Carol M., Hamosh, Ada, Kerner, Berit, MacArthur, Jacqueline A. L., Maglott, Donna R., Mons, Barend, Rehm, Heidi L., Schofield, Paul N., Searle, Beverly A., Smedley, Damian, Smith, Cynthia L., Bernstein, Inge Thomsen, Zankl, Andreas, and Zhao, Eric Y.

Published
2013
Full Text
View/download PDF

88. The NIH genetic testing registry: a new, centralized database of genetic tests to enable access to comprehensive information and improve transparency

Author

Rubinstein, Wendy S., Maglott, Donna R., Lee, Jennifer M., Kattman, Brandi L., Malheiro, Adriana J., Ovetsky, Michael, Hem, Vichet, Gorelenkov, Viatcheslav, Song, Guangfeng, Wallin, Craig, Husain, Nora, Chitipiralla, Shanmuga, Katz, Kenneth S., Hoffman, Douglas, Jang, Wonhee, Johnson, Mark, Karmanov, Fedor, Ukrainchik, Alexander, Denisenko, Mikhail, Fomous, Cathy, Hudson, Kathy, and Ostell, James M.

Published
2013
Full Text
View/download PDF

90. Initial sequencing and comparative analysis of the mouse genome

Author

Chinwalla, Asif T., Cook, Lisa L., Delehaunty, Kimberly D., Fewell, Ginger A., Fulton, Lucinda A., Fulton, Robert S., Graves, Tina A., Hillier, LaDeana W., Mardis, Elaine R., McPherson, John D., Miner, Tracie L., Nash, William E., Nelson, Joanne O., Nhan, Michael N., Pepin, Kymberlie H., Pohl, Craig S., Ponce, Tracy C., Schultz, Brian, Thompson, Johanna, Trevaskis, Evanne, Waterston, Robert H., Wendl, Michael C., Wilson, Richard K., Yang, Shiaw-Pyng, An, Peter, Berry, Eric, Birren, Bruce, Bloom, Toby, Brown, Daniel G., Butler, Jonathan, Daly, Mark, David, Robert, Deri, Justin, Dodge, Sheila, Foley, Karen, Gage, Diane, Gnerre, Sante, Holzer, Timothy, Jaffe, David B., Kamal, Michael, Karlsson, Elinor K., Kells, Cristyn, Kirby, Andrew, Kulbokas, III, Edward J., Lander, Eric S., Landers, Tom, Leger, J. P., Levine, Rosie, Lindblad-Toh, Kerstin, Mauceli, Evan, Mayer, John H., McCarthy, Megan, Meldrim, Jim, Mesirov, Jill P., Nicol, Robert, Nusbaum, Chad, Seaman, Steven, Sharpe, Ted, Sheridan, Andrew, Singer, Jonathan B., Santos, Ralph, Spencer, Brian, Stange-Thomann, Nicole, Vinson, Jade P., Wade, Claire M., Wierzbowski, Jamey, Wyman, Dudley, Zody, Michael C., Birney, Ewan, Goldman, Nick, Kasprzyk, Arkadiusz, Mongin, Emmanuel, Rust, Alistair G., Slater, Guy, Stabenau, Arne, Ureta-Vidal, Abel, Whelan, Simon, Ainscough, Rachel, Attwood, John, Bailey, Jonathon, Barlow, Karen, Beck, Stephan, Burton, John, Clamp, Michele, Clee, Christopher, Coulson, Alan, Cuff, James, Curwen, Val, Cutts, Tim, Davies, Joy, Eyras, Eduardo, Grafham, Darren, Gregory, Simon, Hubbard, Tim, Hunt, Adrienne, Jones, Matthew, Joy, Ann, Leonard, Steven, Lloyd, Christine, Matthews, Lucy, McLaren, Stuart, McLay, Kirsten, Meredith, Beverley, Mullikin, James C., Ning, Zemin, Oliver, Karen, Overton-Larty, Emma, Plumb, Robert, Potter, Simon, Quail, Michael, Rogers, Jane, Scott, Carol, Searle, Steve, Shownkeen, Ratna, Sims, Sarah, Wall, Melanie, West, Anthony P., Willey, David, Williams, Sophie, Abril, Josep F., Guigo, Roderic, Parra, Genis, Agarwal, Pankaj, Agarwala, Richa, Church, Deanna M., Hlavina, Wratko, Maglott, Donna R., Sapojnikov, Victor, Alexandersson, Marina, Pachter, Lior, Antonarakis, Stylianos E., Dermitzakis, Emmanouil T., Reymond, Alexandre, Ucla, Catherine, Baertsch, Robert, Diekhans, Mark, Furey, Terrence S., Hinrichs, Angela, Hsu, Fan, Karolchik, Donna, Kent, W. James, Roskin, Krishna M., Schwartz, Matthias S., Sugnet, Charles, Weber, Ryan J., Bork, Peer, Letunic, Ivica, Suyama, Mikita, Torrents, David, Zdobnov, Evgeny M., Botcherby, Marc, Brown, Stephen D., Campbell, Robert D., Jackson, Ian, Bray, Nicolas, Couronne, Olivier, Dubchak, Inna, Poliakov, Alex, Rubin, Edward M., Brent, Michael R., Flicek, Paul, Keibler, Evan, Korf, Ian, Batalov, S., Bult, Carol, Frankel, Wayne N., Carninci, Piero, Hayashizaki, Yoshihide, Kawai, Jun, Okazaki, Yasushi, Cawley, Simon, Kulp, David, Wheeler, Raymond, Chiaromonte, Francesca, Collins, Francis S., Felsenfeld, Adam, Guyer, Mark, Peterson, Jane, Wetterstrand, Kris, Copley, Richard R., Mott, Richard, Dewey, Colin, Dickens, Nicholas J., Emes, Richard D., Goodstadt, Leo, Ponting, Chris P., Winter, Eitan, Dunn, Diane M., von Niederhausern, Andrew C., Weiss, Robert B., Eddy, Sean R., Johnson, L. Steven, Jones, Thomas A., Elnitski, Laura, Kolbe, Diana L., Eswara, Pallavi, Miller, Webb, O'Connor, Michael J., Schwartz, Scott, Muzny, Donna M., Glusman, Gustavo, Smit, Arian, Green, Eric D., Hardison, Ross C., Yang, Shan, Haussler, David, Hua, Axin, Roe, Bruce A., Kucherlapati, Raju S., Montgomery, Kate T., Li, Jia, Li, Ming, Lucas, Susan, Ma, Bin, McCombie, W. Richard, Morgan, Michael, Pevzner, Pavel, Tesler, Glenn, Schultz, Jorg, Smith, Douglas R., Tromp, John, and Worley, Kim C.

Subjects
Environmental issues, Science and technology, Zoology and wildlife conservation
Abstract

Author(s): Mouse Genome Sequencing Consortium ; Genome Sequencing Center: ; Asif T. Chinwalla [1, 47]; Lisa L. Cook [1]; Kimberly D. Delehaunty [1]; Ginger A. Fewell [1]; Lucinda A. Fulton [...]

Published
2002
Full Text
View/download PDF

91. Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs

Author

Okazaki, Y., Furuno, M., Kasukawa, T., Adachi, J., Bono, H., Kondo, S., Nikaido, I., Osato, N., Saito, R., Suzuki, H., Yamanaka, I., Kiyosawa, H., Yagi, K., Tomaru, Y., Hasegawa, Y., Nogami, A., Schonbach, C., Gojobori, T., Baldarelli, R., Hill, D. P., Bult, C., Hume, D. A., Quackenbush, J., Schriml, L. M., Kanapin, A., Matsuda, H., Batalov, S., Beisel, K. W., Blake, J. A., Bradt, D., Brusic, V., Chothia, C., Corbani, L. E., Cousins, S., Dalla, E., Dragani, T. A., Fletcher, C. F., Forrest, A., Frazer, K. S., Gaasterland, T., Gariboldi, M., Gissi, C., Godzik, A., Gough, J., Grimmond, S., Gustincich, S., Hirokawa, N., Jackson, I. J., Jarvis, E. D., Kanai, A., Kawaji, H., Kawasawa, Y., Kedzierski, R. M., King, B. L., Konagaya, A., Kurochkin, I. V., Lee, Y., Lenhard, B., Lyons, P. A., Maglott, D. R., Maltais, L., Marchionni, L., McKenzie, L., Miki, H., Nagashima, T., Numata, K., Okido, T., Pavan, W. J., Pertea, G., Pesole, G., Petrovsky, N., Pillai, R., Pontius, J. U., Qi, D., Ramachandran, S., Ravasi, T., Reed, J. C., Reed, D. J., Reid, J., Ring, B. Z., Ringwald, M., Sandelin, A., Schneider, C., Semple, C. A. M., Setou, M., Shimada, K., Sultana, R., Takenaka, Y., Taylor, M. S., Teasdale, R. D., Tomita, M., Verardo, R., Wagner, L., Wahlestedt, C., Wang, Y., Watanabe, Y., Wells, C., Wilming, L. G., Wynshaw-Boris, A., Yanagisawa, M., Yang, I., Yang, L., Yuan, Z., Zavolan, M., Zhu, Y., Zimmer, A., Carninci, P., Hayatsu, N., Hirozane-Kishikawa, T., Konno, H., Nakamura, M., Sakazume, N., Sato, K., Shiraki, T., Waki, K., Kawai, J., Aizawa, K., Arakawa, T., Fukuda, S., Hara, A., Hashizume, W., Imotani, K., Ishii, Y., Itoh, M., Kagawa, I., Miyazaki, A., Sakai, K., Sasaki, D., Shibata, K., Shinagawa, A., Yasunishi, A., Yoshino, M., Waterston, R., Lander, E. S., Rogers, J., Birney, E., and Hayashizaki, Y.

Subjects
Environmental issues, Science and technology, Zoology and wildlife conservation
Abstract

Author(s): The FANTOM Consortium and the RIKEN Genome Exploration Research Group Phase I & II Team*; FANTOM Consortium:; Y. Okazaki [1, 2]; M. Furuno [1]; T. Kasukawa [1, 3]; J. [...]

Published
2002
Full Text
View/download PDF

93. Database resources of the National Center for Biotechnology Information

Author

Sayers, Eric W., Barrett, Tanya, Benson, Dennis A., Bolton, Evan, Bryant, Stephen H., Canese, Kathi, Chetvernin, Vyacheslav, Church, Deanna M., DiCuccio, Michael, Federhen, Scott, Feolo, Michael, Fingerman, Ian M., Geer, Lewis Y., Helmberg, Wolfgang, Kapustin, Yuri, Krasnov, Sergey, Landsman, David, Lipman, David J., Lu, Zhiyong, Madden, Thomas L., Madej, Tom, Maglott, Donna R., Marchler-Bauer, Aron, Miller, Vadim, Karsch-Mizrachi, Ilene, Ostell, James, Panchenko, Anna, Phan, Lon, Pruitt, Kim D., Schuler, Gregory D., Sequeira, Edwin, Sherry, Stephen T., Shumway, Martin, Sirotkin, Karl, Slotta, Douglas, Souvorov, Alexandre, Starchenko, Grigory, Tatusova, Tatiana A., Wagner, Lukas, Wang, Yanli, Wilbur, W. John, Yaschenko, Eugene, and Ye, Jian

Published
2012
Full Text
View/download PDF

94. Deciphering the colon cancer genes—report of the InSiGHT-Human Variome Project Workshop, UNESCO, Paris 2010

Author

Kohonen-Corish, Maija R.J., Macrae, Finlay, Genuardi, Maurizio, Aretz, Stefan, Bapat, Bharati, Bernstein, Inge T., Burn, John, Cotton, Richard G.H., den Dunnen, Johan T., Frebourg, Thierry, Greenblatt, Marc S., Hofstra, Robert, Holinski-Feder, Elke, Lappalainen, Ilkka, Lindblom, Annika, Maglott, Donna, Møller, Pål, Morreau, Hans, Möslein, Gabriela, Sijmons, Rolf, Spurdle, Amanda B., Tavtigian, Sean, Tops, Carli M.J., Weber, Thomas K., de Wind, Niels, and Woods, Michael O.

Published
2011
Full Text
View/download PDF

95. Database resources of the National Center for Biotechnology Information

Author

Sayers, Eric W., Barrett, Tanya, Benson, Dennis A., Bolton, Evan, Bryant, Stephen H., Canese, Kathi, Chetvernin, Vyacheslav, Church, Deanna M., DiCuccio, Michael, Federhen, Scott, Feolo, Michael, Fingerman, Ian M., Geer, Lewis Y., Helmberg, Wolfgang, Kapustin, Yuri, Landsman, David, Lipman, David J., Lu, Zhiyong, Madden, Thomas L., Madej, Tom, Maglott, Donna R., Marchler-Bauer, Aron, Miller, Vadim, Mizrachi, Ilene, Ostell, James, Panchenko, Anna, Phan, Lon, Pruitt, Kim D., Schuler, Gregory D., Sequeira, Edwin, Sherry, Stephen T., Shumway, Martin, Sirotkin, Karl, Slotta, Douglas, Souvorov, Alexandre, Starchenko, Grigory, Tatusova, Tatiana A., Wagner, Lukas, Wang, Yanli, Wilbur, W. John, Yaschenko, Eugene, and Ye, Jian

Published
2011
Full Text
View/download PDF

97. How the NIH Genetic Testing Registry and Medical Genetics Summaries can help oncologists adopt pharmacogenetics guidelines.

Author

Malheiro, Adriana Jose, primary, Dean, Laura Charlotte, additional, Hoeppner, Marilu A, additional, Lyoshin, Vitaliy, additional, Gu, Baoshan, additional, Chen, Chao, additional, Liu, Chunlei, additional, Maddipatla, Zenith, additional, Shi, Wenyao, additional, Jang, Wonhee, additional, Hoffman, Douglas, additional, Zhou, George, additional, Chitipiralla, Shanmuga, additional, Mitchell, Joe, additional, Maglott, Donna R., additional, and Kattman, Brandi L., additional

Published
2020
Full Text
View/download PDF

98. Designed signaling aptamers that transduce molecular recognition to changes in fluorescence intensity

Author

Jhaveri, Sulay D., Kirby, Romy, Conrad, Rick, Maglott, Emily J., Bowser, Michael, Kennedy, Robert T., Glick, Gary, and Ellington, Andrew D.

Subjects
Adenosine -- Research, DNA -- Research, Fluorescence -- Research, Ligands -- Research, RNA -- Research, Chemistry
Abstract

Research is presented describing the formation of aptamers which signal the presence of cognate ligands in solution and which contain fluorescent reporters. An RNA- and DNA-produced anti-adenosine signaling aptamer are each able to selectively indicate the occurrence of adenosine in solution.

Published
2000

99. How to catch all those mutations—the report of the Third Human Variome Project Meeting, UNESCO Paris, May 2010

Author

Kohonen-Corish, Maija R.J., Al-Aama, Jumana Y., Auerbach, Arleen D., Axton, Myles, Barash, Carol Isaacson, Bernstein, Inge, Béroud, Christophe, Burn, John, Cunningham, Fiona, Cutting, Garry R., den Dunnen, Johan T., Greenblatt, Marc S., Kaput, Jim, Katz, Michael, Lindblom, Annika, Macrae, Finlay, Maglott, Donna, Möslein, Gabriela, Povey, Sue, Ramesar, Raj, Richards, Sue, Seminara, Daniela, Sobrido, María-Jesús, Tavtigian, Sean, Taylor, Graham, Vihinen, Mauno, Winship, Ingrid, and Cotton, Richard G.H.

Published
2010
Full Text
View/download PDF

Catalog

Books, media, physical & digital resources
See catalog results