نتائج البحث - Nhat Tran

  • يعرض 1 - 18 نتائج من 18
تنقيح النتائج
  1. 1
    Replica exchange molecular dynamics study of the amyloid beta (11–40) trimer penetrating a membrane

    Replica exchange molecular dynamics study of the amyloid beta (11–40) trimer penetrating a membrane حسب Sơn Tùng Ngô, Huynh Minh Hung, Khoa Nhat Tran, Minh Tho Nguyen

    منشور في 2017
    احصل على النص الكامل احصل على النص الكامل
    Artigo
    أضف إلى المفضلة
    محفوظ في:
  2. 2
    Estimates of Japanese Encephalitis mortality and morbidity: A systematic review and modeling analysis

    Estimates of Japanese Encephalitis mortality and morbidity: A systematic review and modeling analysis حسب Yuwei Cheng, Nhat Tran Minh, Quan Minh Tran, Shreya Khandelwal, Hannah Clapham

    منشور في 2022
    احصل على النص الكامل احصل على النص الكامل
    Revisão
    أضف إلى المفضلة
    محفوظ في:
  3. 3
    Estimates of the global burden of Japanese encephalitis and the impact of vaccination from 2000-2015

    Estimates of the global burden of Japanese encephalitis and the impact of vaccination from 2000-2015 حسب Quan, Tran Minh, Thao, Tran Thi Nhu, Duy, Nguyen Manh, Nhat, Tran Minh, Clapham, Hannah

    منشور في 2020
    احصل على النص الكامل احصل على النص الكامل احصل على النص الكامل
    نص
    أضف إلى المفضلة
    محفوظ في:
  4. 4
    Hepatocyte growth factor and myopia: Genetic association analyses in a caucasian population

    Hepatocyte growth factor and myopia: Genetic association analyses in a caucasian population حسب Yanovitch, Tammy, Li, Yi-Ju, Metlapally, Ravikanth, Abbott, Diana, Viet, Khanh-Nhat Tran, Young, Terri L.

    منشور في 2009
    احصل على النص الكامل احصل على النص الكامل
    نص
    أضف إلى المفضلة
    محفوظ في:
  5. 5
    Mutations in the Novel Mitochondrial Protein REEP1 Cause Hereditary Spastic Paraplegia Type 31

    Mutations in the Novel Mitochondrial Protein REEP1 Cause Hereditary Spastic Paraplegia Type 31 حسب Stephan Züchner, Gaofeng Wang, Khanh-Nhat Tran-Viet, Martha Nance, P. C. Gaskell, Jeffery M. Vance, Allison E. Ashley‐Koch, Margaret A. Pericak‐Vance

    منشور في 2006
    احصل على النص الكامل
    Artigo
    أضف إلى المفضلة
    محفوظ في:
  6. 6
    Functional evidence implicating a novel TOR1A mutation in idiopathic, late-onset focal dystonia

    Functional evidence implicating a novel TOR1A mutation in idiopathic, late-onset focal dystonia حسب Nicole Calakos, Vaishali Patel, Melissa A Gottron, G. Wang, Khanh-Nhat Tran-Viet, D. Brewington, J. Beyer, David C. Steffens, Ranga Krishnan, Stephan Züchner

    منشور في 2009
    احصل على النص الكامل
    Artigo
    أضف إلى المفضلة
    محفوظ في:
  7. 7
    CYP1B1, MYOC, and LTBP2 Mutations in Primary Congenital Glaucoma Patients in the United States

    CYP1B1, MYOC, and LTBP2 Mutations in Primary Congenital Glaucoma Patients in the United States حسب 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

    منشور في 2012
    احصل على النص الكامل
    Artigo
    أضف إلى المفضلة
    محفوظ في:
  8. 8
    Genetic Association of Insulin-like Growth Factor-1 Polymorphisms with High-Grade Myopia in an International Family Cohort

    Genetic Association of Insulin-like Growth Factor-1 Polymorphisms with High-Grade Myopia in an International Family Cohort حسب 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

    منشور في 2010
    احصل على النص الكامل
    Artigo
    أضف إلى المفضلة
    محفوظ في:
  9. 9
    <i>COL1A1</i>and<i>COL2A1</i>Genes and Myopia Susceptibility: Evidence of Association and Suggestive Linkage to the<i>COL2A1</i>Locus

    <i>COL1A1</i>and<i>COL2A1</i>Genes and Myopia Susceptibility: Evidence of Association and Suggestive Linkage to the<i>COL2A1</i>Locus حسب 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

    منشور في 2009
    احصل على النص الكامل
    Artigo
    أضف إلى المفضلة
    محفوظ في:
  10. 10
    Multiple rare SAPAP3 missense variants in trichotillomania and OCD

    Multiple rare SAPAP3 missense variants in trichotillomania and OCD حسب 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

    منشور في 2008
    احصل على النص الكامل
    Revisão
    أضف إلى المفضلة
    محفوظ في:
  11. 11
    Antimicrobial residues and resistance against critically important antimicrobials in non-typhoidal Salmonella from meat sold at wet markets and supermarkets in Vietnam

    Antimicrobial residues and resistance against critically important antimicrobials in non-typhoidal Salmonella from meat sold at wet markets and supermarkets in Vietnam حسب 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

    منشور في 2018
    احصل على النص الكامل احصل على النص الكامل احصل على النص الكامل
    نص
    أضف إلى المفضلة
    محفوظ في:
  12. 12
    Mutations in SCO2 Are Associated with Autosomal-Dominant High-Grade Myopia

    Mutations in SCO2 Are Associated with Autosomal-Dominant High-Grade Myopia حسب 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

    منشور في 2013
    احصل على النص الكامل
    Artigo
    أضف إلى المفضلة
    محفوظ في:
  13. 13
    Whole exome sequencing identifies a mutation for a novel form of corneal intraepithelial dyskeratosis

    Whole exome sequencing identifies a mutation for a novel form of corneal intraepithelial dyskeratosis حسب 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

    منشور في 2013
    احصل على النص الكامل
    Artigo
    أضف إلى المفضلة
    محفوظ في:
  14. 14
    Genome-wide association identifies ATOH7 as a major gene determining human optic disc size

    Genome-wide association identifies ATOH7 as a major gene determining human optic disc size حسب 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

    منشور في 2010
    احصل على النص الكامل احصل على النص الكامل
    Revisão
    أضف إلى المفضلة
    محفوظ في:
  15. 15
    REEP1 mutation spectrum and genotype/phenotype correlation in hereditary spastic paraplegia type 31

    REEP1 mutation spectrum and genotype/phenotype correlation in hereditary spastic paraplegia type 31 حسب 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

    منشور في 2008
    احصل على النص الكامل احصل على النص الكامل
    Artigo
    أضف إلى المفضلة
    محفوظ في:
  16. 16
    Angiopoietin receptor TEK mutations underlie primary congenital glaucoma with variable expressivity

    Angiopoietin receptor TEK mutations underlie primary congenital glaucoma with variable expressivity حسب 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

    منشور في 2016
    احصل على النص الكامل احصل على النص الكامل
    Artigo
    أضف إلى المفضلة
    محفوظ في:
  17. 17
    PRMT5 inhibition disrupts splicing and stemness in glioblastoma

    PRMT5 inhibition disrupts splicing and stemness in glioblastoma حسب 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

    منشور في 2021
    احصل على النص الكامل احصل على النص الكامل
    Artigo
    أضف إلى المفضلة
    محفوظ في:
  18. 18
    Genetic surveillance in the Greater Mekong subregion and South Asia to support malaria control and elimination

    Genetic surveillance in the Greater Mekong subregion and South Asia to support malaria control and elimination حسب 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

    منشور في 2021
    احصل على النص الكامل احصل على النص الكامل احصل على النص الكامل
    نص
    أضف إلى المفضلة
    محفوظ في:

أدوات البحث: