Hasil Pencarian - NISC Comparative Sequencing Program
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Alternative Isoform Analysis of Ttc8 Expression in the Rat Pineal Gland Using a Multi-Platform Sequencing Approach Reveals Neural Regulation. oleh Stephen W Hartley, James C Mullikin, David C Klein, Morgan Park, NISC Comparative Sequencing Program, Steven L Coon
Diterbitkan 2016-01-01
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Early history of mammals is elucidated with the ENCODE multiple species sequencing data. oleh Sergey Nikolaev, Juan I Montoya-Burgos, Elliott H Margulies, NISC Comparative Sequencing Program, Jacques Rougemont, Bruno Nyffeler, Stylianos E Antonarakis
Diterbitkan 2007-01-01
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MEK inhibition remodels the active chromatin landscape and induces SOX10 genomic recruitment in BRAF(V600E) mutant melanoma cells oleh Temesgen D. Fufa, Laura L. Baxter, Julia C. Wedel, Derek E. Gildea, NISC Comparative Sequencing Program, Stacie K. Loftus, William J. Pavan
Diterbitkan 2019-08-01
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Roving methyltransferases generate a mosaic epigenetic landscape and influence evolution in Bacteroides fragilis group oleh Michael J. Tisza, Derek D. N. Smith, Andrew E. Clark, Jung-Ho Youn, NISC Comparative Sequencing Program, Pavel P. Khil, John P. Dekker
Diterbitkan 2023-07-01
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Low-level variant calling for non-matched samples using a position-based and nucleotide-specific approach oleh Jeffrey N. Dudley, Celine S. Hong, Marwan A. Hawari, Jasmine Shwetar, Julie C. Sapp, Justin Lack, Henoke Shiferaw, NISC Comparative Sequencing Program, Jennifer J. Johnston, Leslie G. Biesecker
Diterbitkan 2021-04-01
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A mouse model of occult intestinal colonization demonstrating antibiotic-induced outgrowth of carbapenem-resistant Enterobacteriaceae oleh Choon K. Sim, Sara Saheb Kashaf, Apollo Stacy, Diana M. Proctor, Alexandre Almeida, Nicolas Bouladoux, Mark Chen, NISC Comparative Sequencing Program, Robert D. Finn, Yasmine Belkaid, Sean Conlan, Julia A. Segre
Diterbitkan 2022-03-01
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A novel de novo TP63 mutation in whole‐exome sequencing of a Syrian family with Oral cleft and ectrodactyly oleh Claire L. Simpson, Danielle C. Kimble, Settara C. Chandrasekharappa, NISC Comparative Sequencing Program, Khalid Alqosayer, Emily Holzinger, Blake Carrington, John McElderry, Raman Sood, Ghiath Al‐Souqi, Hasan Albacha‐Hejazi, Joan E. Bailey‐Wilson
Diterbitkan 2023-08-01
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Primary oxidative phosphorylation defects lead to perturbations in the human B cell repertoire oleh Eliza M. Gordon-Lipkin, Payal Banerjee, Jose Luis Marin Franco, Tatiana Tarasenko, Shannon Kruk, Elizabeth Thompson, Derek E. Gildea, Suiyuan Zhang, Tyra G. Wolfsberg, NISC Comparative Sequencing Program, Willy A. Flegel, Peter J. McGuire
Diterbitkan 2023-07-01
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Gene-Specific Substitution Profiles Describe the Types and Frequencies of Amino Acid Changes during Antibody Somatic Hypermutation oleh Zizhang Sheng, Zizhang Sheng, Chaim A. Schramm, Chaim A. Schramm, Chaim A. Schramm, Rui Kong, NISC Comparative Sequencing Program, James C. Mullikin, John R. Mascola, Peter D. Kwong, Peter D. Kwong, Lawrence Shapiro, Lawrence Shapiro, Lawrence Shapiro
Diterbitkan 2017-05-01
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A rare myelin protein zero (MPZ) variant alters enhancer activity in vitro and in vivo. oleh Anthony Antonellis, Megan Y Dennis, Grzegorz Burzynski, Jimmy Huynh, Valerie Maduro, Chani J Hodonsky, Mehrdad Khajavi, Kinga Szigeti, Sandeep Mukkamala, Seneca L Bessling, William J Pavan, Andrew S McCallion, James R Lupski, Eric D Green, NISC Comparative Sequencing Program
Diterbitkan 2010-12-01
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Balancing selection maintains a form of ERAP2 that undergoes nonsense-mediated decay and affects antigen presentation. oleh Aida M Andrés, Megan Y Dennis, Warren W Kretzschmar, Jennifer L Cannons, Shih-Queen Lee-Lin, Belen Hurle, NISC Comparative Sequencing Program, Pamela L Schwartzberg, Scott H Williamson, Carlos D Bustamante, Rasmus Nielsen, Andrew G Clark, Eric D Green
Diterbitkan 2010-10-01
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A direct link between MITF, innate immunity, and hair graying. oleh Melissa L Harris, Temesgen D Fufa, Joseph W Palmer, Sandeep S Joshi, Denise M Larson, Arturo Incao, Derek E Gildea, Niraj S Trivedi, Autumne N Lee, Chi-Ping Day, Helen T Michael, Thomas J Hornyak, Glenn Merlino, NISC Comparative Sequencing Program, William J Pavan
Diterbitkan 2018-05-01
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Developmental Pathway of the MPER-Directed HIV-1-Neutralizing Antibody 10E8. oleh Cinque Soto, Gilad Ofek, M Gordon Joyce, Baoshan Zhang, Krisha McKee, Nancy S Longo, Yongping Yang, Jinghe Huang, Robert Parks, Joshua Eudailey, Krissey E Lloyd, S Munir Alam, Barton F Haynes, NISC Comparative Sequencing Program, James C Mullikin, Mark Connors, John R Mascola, Lawrence Shapiro, Peter D Kwong
Diterbitkan 2016-01-01
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Genetic modifiers of neurofibromatosis type 1-associated café-au-lait macule count identified using multi-platform analysis. oleh Alexander Pemov, Heejong Sung, Paula L Hyland, Jennifer L Sloan, Sarah L Ruppert, Andrea M Baldwin, Joseph F Boland, Sara E Bass, Hyo Jung Lee, Kristine M Jones, Xijun Zhang, NISC Comparative Sequencing Program, James C Mullikin, Brigitte C Widemann, Alexander F Wilson, Douglas R Stewart
Diterbitkan 2014-10-01
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A genome catalog of the early-life human skin microbiome oleh Zeyang Shen, Lukian Robert, Milan Stolpman, You Che, Katrina J. Allen, Richard Saffery, Audrey Walsh, Angela Young, Jana Eckert, Clay Deming, Qiong Chen, Sean Conlan, Karen Laky, Jenny Min Li, Lindsay Chatman, Sara Saheb Kashaf, NISC Comparative Sequencing Program, VITALITY team, Heidi H. Kong, Pamela A. Frischmeyer-Guerrerio, Kirsten P. Perrett, Julia A. Segre
Diterbitkan 2023-11-01
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Whole-exome sequencing identifies homozygous AFG3L2 mutations in a spastic ataxia-neuropathy syndrome linked to mitochondrial m-AAA proteases. oleh Tyler Mark Pierson, David Adams, Florian Bonn, Paola Martinelli, Praveen F Cherukuri, Jamie K Teer, Nancy F Hansen, Pedro Cruz, James C Mullikin For The Nisc Comparative Sequencing Program, Robert W Blakesley, Gretchen Golas, Justin Kwan, Anthony Sandler, Karin Fuentes Fajardo, Thomas Markello, Cynthia Tifft, Craig Blackstone, Elena I Rugarli, Thomas Langer, William A Gahl, Camilo Toro
Diterbitkan 2011-10-01
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Sequencing of candidate chromosome instability genes in endometrial cancers reveals somatic mutations in ESCO1, CHTF18, and MRE11A. oleh Jessica C Price, Lana M Pollock, Meghan L Rudd, Sarah K Fogoros, Hassan Mohamed, Christin L Hanigan, Matthieu Le Gallo, NIH Intramural Sequencing Center (NISC) Comparative Sequencing Program, Suiyuan Zhang, Pedro Cruz, Praveen F Cherukuri, Nancy F Hansen, Kirk J McManus, Andrew K Godwin, Dennis C Sgroi, James C Mullikin, Maria J Merino, Philip Hieter, Daphne W Bell
Diterbitkan 2014-01-01
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