Výsledky vyhledávání - Margaret Gibson
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RNA-seq Reveals Novel Transcriptome of Genes and Their Isoforms in Human Pulmonary Microvascular Endothelial Cells Treated with Thrombin Autor Li Qin Zhang, Dilyara Cheranova, Margaret Gibson, Shinghua Ding, Daniel P. Heruth, Deyu Fang, Shui Qing Ye
Vydáno 2012Artigo -
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ASCL2 reciprocally controls key trophoblast lineage decisions during hemochorial placenta development Autor Kaela M. Varberg, Khursheed Iqbal, Masanaga Muto, Mikaela E. Simon, Regan L. Scott, Keisuke Kozai, Ruhul Choudhury, John Aplin, Rebecca Biswell, Margaret Gibson, Hiroaki Okae, Takahiro Arima, Jay L. Vivian, Elin Grundberg, Michael J. Soares
Vydáno 2021Artigo -
4
Constellation: a tool for rapid, automated phenotype assignment of a highly polymorphic pharmacogene, CYP2D6, from whole-genome sequences Autor Greyson P Twist, Andrea Gaedigk, Neil Miller, Emily Farrow, Laurel K. Willig, Darrell L. Dinwiddie, Josh E Petrikin, Sarah Soden, Suzanne Herd, Margaret Gibson, Julie A. Cakici, Amanda K. Riffel, J. Steven Leeder, Deendayal Dinakarpandian, Stephen F. Kingsmore
Vydáno 2016Artigo -
5
Single-cell analysis of human adipose tissue identifies depot- and disease-specific cell types Autor Jinchu Vijay, Marie‐Frédérique Gauthier, Rebecca Biswell, Daniel Louiselle, Jeffrey Johnston, Warren Cheung, Bradley Belden, Albéna Pramatarova, Laurent Biertho, Margaret Gibson, Marie-Michelle Simon, Haig Djambazian, Alfredo Staffa, Guillaume Bourque, Anita Laitinen, Johanna Nystedt, Marie‐Claude Vohl, Jason D. Fraser, Tomi Pastinen, André Tchernof, Elin Grundberg
Vydáno 2019Artigo -
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A 26-hour system of highly sensitive whole genome sequencing for emergency management of genetic diseases Autor Neil Miller, Emily Farrow, Margaret Gibson, Laurel K. Willig, Greyson P Twist, Byunggil Yoo, T. C. Marrs, Shane Corder, Lisa Ann Krivohlavek, Adam Walter, Josh E Petrikin, Carol Saunders, Isabelle Thiffault, Sarah Soden, Laurie D. Smith, Darrell L. Dinwiddie, Suzanne Herd, Julie A. Cakici, Severine Catreux, Mike Ruehle, Stephen F. Kingsmore
Vydáno 2015Artigo -
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Direct haplotype-resolved 5-base HiFi sequencing for genome-wide profiling of hypermethylation outliers in a rare disease cohort Autor Warren Cheung, Adam F. Johnson, William J. Rowell, Emily Farrow, Richard Hall, Ana S.A. Cohen, John C. Means, Tricia Zion, Daniel M. Portik, Christopher T. Saunders, Boryana Koseva, Chengpeng Bi, Tina K. Truong, Carl Schwendinger-Schreck, Byunggil Yoo, Jeffrey Johnston, Margaret Gibson, Gilad D. Evrony, William B. Rizzo, Isabelle Thiffault, Scott T. Younger, Tom Curran, Aaron M. Wenger, Elin Grundberg, Tomi Pastinen
Vydáno 2023Artigo -
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Genomic answers for children: Dynamic analyses of >1000 pediatric rare disease genomes Autor Ana S.A. Cohen, Emily Farrow, Ahmed Abdelmoity, Joseph T. Alaimo, Shivarajan Amudhavalli, John T. Anderson, Lalit Bansal, Lauren Bartik, Primo Baybayan, Bradley Belden, Courtney Berrios, Rebecca Biswell, Pawel Buczkowicz, Orion J. Buske, Shreyasee Chakraborty, Warren Cheung, Keith A. Coffman, Ashley M. Cooper, Laura Cross, Tom Curran, Thuy Tien T. Dang, Mary Elfrink, Kendra Engleman, Erin Fecske, Cynthia Fieser, Keely Fitzgerald, Emily Fleming, Randi Gadea, Jennifer Gannon, Rose Gelineau‐Morel, Margaret Gibson, Jeffrey A. Goldstein, Elin Grundberg, Kelsee Halpin, Brian S. Harvey, Bryce A. Heese, Wendy Hein, Suzanne Herd, Susan Hughes, Mohammed Ilyas, Jill D. Jacobson, Janda Jenkins, Jiang Shao, Jeffrey Johnston, Kathryn Keeler, Jonas Korlach, Jennifer Kussmann, Christine Lambert, Caitlin E. Lawson, Jean‐Baptiste Le Pichon, J. Steven Leeder, Vicki C. Little, Daniel Louiselle, Michael Lypka, Brittany McDonald, Neil Miller, Ann Modrcin, Annapoorna Nair, Shelby H. Neal, Christopher M. Oermann, Donna Pacicca, Kailash Pawar, Nyshele Posey, Nigel Price, Laura Puckett, Julio Quezada, Nikita Raje, William J. Rowell, Eric T. Rush, Venkatesh Sampath, Carol Saunders, Caitlin Schwager, Richard M. Schwend, Elizabeth Shaffer, Craig Smail, Sarah Soden, Meghan E. Strenk, Bonnie Sullivan, Brooke Sweeney, Jade Tam‐Williams, Adam M. Walter, Holly Welsh, Aaron M. Wenger, Laurel K. Willig, Yun Yan, Scott T. Younger, Dihong Zhou, Tricia Zion, Isabelle Thiffault, Tomi Pastinen
Vydáno 2022Artigo
Vyhledávací nástroje:
Související témata
Biology
Genetics
Gene
Genome
Medicine
Cell biology
Computational biology
DNA sequencing
Genotype
Internal medicine
Copy-number variation
Disease
Gene expression
Haplotype
Immunology
Single-nucleotide polymorphism
Whole genome sequencing
1000 Genomes Project
3T3-L1
Adipocyte
Adipose tissue
Allele
Bioinformatics
Cancer research
Cell
Cell type
Cohort
Computer science
CpG site
DNA methylation