Хайлтын үр дүнгүүд - Nhat Tran
- 18-н 1 - 18 үр дүнгүүдийг харуулж байна
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CYP1B1, MYOC, and LTBP2 Mutations in Primary Congenital Glaucoma Patients in the United States -н Sing-Hui Lim, Khanh-Nhat Tran-Viet, Tammy L. Yanovitch, Sharon F. Freedman, Thomas Klemm, Whitney Call, Caldwell Powell, Ajay Ravichandran, Ravikanth Metlapally, Erica B. Nading, Steve Rozen, Terri L. Young
Хэвлэсэн 2012Artigo -
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Genetic Association of Insulin-like Growth Factor-1 Polymorphisms with High-Grade Myopia in an International Family Cohort -н Ravikanth Metlapally, Chang‐Seok Ki, Yi‐Ju Li, Khanh-Nhat Tran-Viet, Diana Abbott, François Malecaze, Patrick Calvas, David A. Mackey, Thomas Rosenberg, Sandrine Paget, Jeremy A. Guggenheim, Terri L. Young
Хэвлэсэн 2010Artigo -
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<i>COL1A1</i>and<i>COL2A1</i>Genes and Myopia Susceptibility: Evidence of Association and Suggestive Linkage to the<i>COL2A1</i>Locus -н Ravikanth Metlapally, Yi‐Ju Li, Khanh-Nhat Tran-Viet, Diana Abbott, Gregory R. Czaja, François Malecaze, Patrick Calvas, David A. Mackey, Thomas Rosenberg, Sandrine Paget, Tetyana Zayats, Michael J. Owen, Jeremy A. Guggenheim, Terri L. Young
Хэвлэсэн 2009Artigo -
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Multiple rare SAPAP3 missense variants in trichotillomania and OCD -н Stephan Züchner, Jens R. Wendland, Allison E. Ashley‐Koch, Amanda Collins, Khanh-Nhat Tran-Viet, Kaia S. Quinn, Kiara R. Timpano, Michael L. Cuccaro, Margaret A. Pericak‐Vance, David C. Steffens, K. Ranga Krishnan, Guoping Feng, Dennis L. Murphy
Хэвлэсэн 2008Revisão -
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Antimicrobial residues and resistance against critically important antimicrobials in non-typhoidal Salmonella from meat sold at wet markets and supermarkets in Vietnam -н Nhung, Nguyen Thi, Van, Nguyen Thi Bich, Cuong, Nguyen Van, Duong, Truong Thi Quy, Nhat, Tran Thi, Hang, Tran Thi Thu, Nhi, Nguyen Thi Hong, Kiet, Bach Tuan, Hien, Vo Be, Ngoc, Pham Thi, Campbell, James, Thwaites, Guy, Carrique-Mas, Juan
Хэвлэсэн 2018текст -
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Mutations in SCO2 Are Associated with Autosomal-Dominant High-Grade Myopia -н Khanh-Nhat Tran-Viet, Caldwell Powell, Veluchamy A. Barathi, Thomas Klemm, Sebastian Maurer‐Stroh, Vachiranee Limviphuvadh, Vincent Soler, Candice Ho, Tammy L. Yanovitch, Georg Schneider, Yi‐Ju Li, Erica B. Nading, Ravikanth Metlapally, Seang‐Mei Saw, Liang Kee Goh, Steve Rozen, Terri L. Young
Хэвлэсэн 2013Artigo -
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Whole exome sequencing identifies a mutation for a novel form of corneal intraepithelial dyskeratosis -н Vincent Soler, Khanh-Nhat Tran-Viet, Stéphane Galiacy, Vachiranee Limviphuvadh, Thomas Klemm, Elizabeth St.Germain, Pierre Fournié, Céline Guillaud, Sebastian Maurer‐Stroh, Felicia Hawthorne, Cyrielle Suarez, B Kantelip, Natalie A. Afshari, Isabelle Creveaux, Xiaoyan Luo, Weihua Meng, Patrick Calvas, Myriam Cassagne, Jean-Louis Arné, Steve Rozen, François Malecaze, Terri L. Young
Хэвлэсэн 2013Artigo -
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Genome-wide association identifies ATOH7 as a major gene determining human optic disc size -н Stuart MacGregor, Alex W. Hewitt, Pirro G. Hysi, Jonathan B. Ruddle, Sarah E. Medland, Anjali K. Henders, Scott D. Gordon, Toby Andrew, Brian McEvoy, Paul G. Sanfilippo, Francis Carbonaro, Vikas Tah, Yi‐Ju Li, Sonya L. Bennett, Jamie E. Craig, Grant W. Montgomery, Khanh-Nhat Tran-Viet, Nadean L. Brown, Timothy D. Spector, Nicholas G. Martin, Terri L. Young, Christopher J. Hammond, David A. Mackey
Хэвлэсэн 2010Revisão -
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REEP1 mutation spectrum and genotype/phenotype correlation in hereditary spastic paraplegia type 31 -н Christian Beetz, Rebecca Schüle, Tine Deconinck, Khanh-Nhat Tran-Viet, Hui Zhu, Berry Kremer, Suzanna G.M. Frints, Wendy A.G. van Zelst–Stams, P. Byrne, Susanne Otto, Anders O.H. Nygren, Jonathan Baets, Katrien Smets, Berten Ceulemans, Bernard Dan, Narasimhan Nagan, Jan Kassubek, Sven Klimpe, Thomas Klopstock, Henning Stolze, Hubert J.M. Smeets, C. T. R. M. Schrander‐Stumpel, Michael Hutchinson, Bart P.C. van de Warrenburg, Corey Braastad, Thomas Deufel, Margaret A. Pericak‐Vance, Lüdger Schöls, Peter De Jonghe, Stephan Züchner
Хэвлэсэн 2008Artigo -
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Angiopoietin receptor TEK mutations underlie primary congenital glaucoma with variable expressivity -н Tomokazu Souma, Stuart W. Tompson, Benjamin R. Thomson, Owen M. Siggs, Krishnakumar Kizhatil, Shinji Yamaguchi, Liang Feng, Vachiranee Limviphuvadh, Kristina N. Whisenhunt, Sebastian Maurer‐Stroh, Tammy L. Yanovitch, Luba Kalaydjieva, Dimitar N. Azmanov, Simone Finzi, Lucia Mauri, Shahrbanou Javadiyan, Emmanuelle Souzeau, Tiger Zhou, Alex W. Hewitt, Bethany A. Kloss, Kathryn P. Burdon, David A. Mackey, Keri F. Allen, Jonathan B. Ruddle, Sing-Hui Lim, Steve Rozen, Khanh-Nhat Tran-Viet, Xiaorong Liu, Simon W. M. John, Janey L. Wiggs, Francesca Pasutto, Jamie E. Craig, Jing Jin, Susan E. Quaggin, Terri L. Young
Хэвлэсэн 2016Artigo -
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PRMT5 inhibition disrupts splicing and stemness in glioblastoma -н Patty Sachamitr, Jolene Caifeng Ho, Felipe E. Ciamponi, Wail Ba-Alawi, Fiona J. Coutinho, Paul Guilhamon, Michelle Kushida, Florence M.G. Cavalli, Lilian Lee, Naghmeh Rastegar, Victoria Vu, María Sánchez‐Osuna, Jasmin Coulombe‐Huntington, Evgeny Kanshin, Heather Whetstone, Mathieu Durand, P Thibault, Kirsten Hart, Maria Mangos, Joseph Veyhl, Wenjun Chen, Nhat Tran, Bang-Chi Duong, Ahmed Aman, Xinghui Che, Xiaoyang Lan, Owen Whitley, Olga Zaslaver, Dalia Baršytė-Lovejoy, Laura M. Richards, Ian J. Restall, Amy A. Caudy, Hannes Röst, Zahid Bonday, Mark Bernstein, Sunit Das, Michael D. Cusimano, Julian Spears, Gary D. Bader, Trevor J. Pugh, Mike Tyers, Mathieu Lupien, Benjamin Haibe‐Kains, H. Artee Luchman, Samuel Weiss, Katlin B. Massirer, Panagiotis Prinos, C.H. Arrowsmith, Peter B. Dirks
Хэвлэсэн 2021Artigo -
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Genetic surveillance in the Greater Mekong subregion and South Asia to support malaria control and elimination -н Jacob, Christopher G, Thuy-Nhien, Nguyen, Mayxay, Mayfong, Maude, Richard J, Quang, Huynh Hong, Hongvanthong, Bouasy, Vanisaveth, Viengxay, Ngo Duc, Thang, Rekol, Huy, van der Pluijm, Rob, von Seidlein, Lorenz, Fairhurst, Rick, Nosten, François, Hossain, Md Amir, Park, Naomi, Goodwin, Scott, Ringwald, Pascal, Chindavongsa, Keobouphaphone, Newton, Paul, Ashley, Elizabeth, Phalivong, Sonexay, Maude, Rapeephan, Leang, Rithea, Huch, Cheah, Dong, Le Thanh, Nguyen, Kim-Tuyen, Nhat, Tran Minh, Hien, Tran Tinh, Nguyen, Hoa, Zdrojewski, Nicole, Canavati, Sara, Sayeed, Abdullah Abu, Uddin, Didar, Buckee, Caroline, Fanello, Caterina I, Onyamboko, Marie, Peto, Thomas, Tripura, Rupam, Amaratunga, Chanaki, Myint Thu, Aung, Delmas, Gilles, Landier, Jordi, Parker, Daniel M, Chau, Nguyen Hoang, Lek, Dysoley, Suon, Seila, Callery, James, Jittamala, Podjanee, Hanboonkunupakarn, Borimas, Pukrittayakamee, Sasithon, Phyo, Aung Pyae, Smithuis, Frank, Lin, Khin, Thant, Myo, Hlaing, Tin Maung, Satpathi, Parthasarathi, Satpathi, Sanghamitra, Behera, Prativa K, Tripura, Amar, Baidya, Subrata, Valecha, Neena, Anvikar, Anupkumar R, Ul Islam, Akhter, Faiz, Abul, Kunasol, Chanon, Drury, Eleanor, Kekre, Mihir, Ali, Mozam, Love, Katie, Rajatileka, Shavanthi, Jeffreys, Anna E, Rowlands, Kate, Hubbart, Christina S, Dhorda, Mehul, Vongpromek, Ranitha, Kotanan, Namfon, Wongnak, Phrutsamon, Almagro Garcia, Jacob, Pearson, Richard D, Ariani, Cristina V, Chookajorn, Thanat, Malangone, Cinzia, Nguyen, T, Stalker, Jim, Jeffery, Ben, Keatley, Jonathan, Johnson, Kimberly J, Muddyman, Dawn, Chan, Xin Hui S, Sillitoe, John, Amato, Roberto, Simpson, Victoria, Gonçalves, Sonia, Rockett, Kirk, Day, Nicholas P, Dondorp, Arjen M, Kwiatkowski, Dominic P, Miotto, Olivo
Хэвлэсэн 2021текст
Хайх хэрэгслүүд:
Холбогдох сэдвүүд
Biology
Genetics
Gene
Medicine
Mutation
Genotype
Neuroscience
Glaucoma
Phenotype
Single-nucleotide polymorphism
Bioinformatics
Cell biology
Cerebral palsy
Exome
Exome sequencing
Exon
Genetic association
Haploinsufficiency
Hereditary spastic paraplegia
Internal medicine
Linkage disequilibrium
Missense mutation
Ophthalmology
Proband
SNP
Spastic
Acoustics
Allele
Alternative splicing
Amyloid (mycology)