Αποτελέσματα αναζήτησης - Farida Abid
- Εμφανίζονται 1 - 4 Αποτελέσματα από 4
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1
LncRNA H19 Alleviates Muscular Dystrophy Through Stabilizing Dystrophin από Zhang, Yaohua, Li, Yajuan, Hu, Qingsong, Xi, Yutao, Xing, Zhen, Zhang, Zhao, Huang, Lisa, Wu, Jianbo, Liang, Ke, Nguyen, Tina K., Egranov, Sergey D., Sun, Chengcao, Zhao, Zilong, Hawke, David H., Li, Jin, Sun, Deqiang, Kim, Jean J., Zhang, Ping, Cheng, Jie, Farida, Abid, Hung, Mien-Chie, Han, Leng, Darabi, Radbod, Lin, Chunru, Yang, Liuqing
Έκδοση 2020Κείμενο -
2
The lncRNA H19 alleviates muscular dystrophy by stabilizing dystrophin από Yaohua Zhang, Yajuan Li, Qingsong Hu, Yutao Xi, Zhen Xing, Zhao Zhang, Lisa A. Huang, Jianbo Wu, Ke Liang, Tina K. Nguyen, Sergey D. Egranov, Cheng‐Cao Sun, Zilong Zhao, David H. Hawke, Jin Li, Deqiang Sun, Ji‐Eun Kim, Ping Zhang, Jie Cheng, Farida Abid, Mien‐Chie Hung, Leng Han, Radbod Darabi, Chunru Lin, Liuqing Yang
Έκδοση 2020Artigo -
3
Clinical exome sequencing reveals locus heterogeneity and phenotypic variability of cohesinopathies από Bo Yuan, Juanita Neira, Davut Pehli̇van, Teresa Santiago‐Sim, Xiaofei Song, Jill A. Rosenfeld, Jennifer E. Posey, Vipulkumar Patel, Weihong Jin, Margaret P Adam, Emma L. Baple, John Dean, Chin‐To Fong, Scott E. Hickey, Louanne Hudgins, Eyby Leon, Suneeta Madan‐Khetarpal, Lettie E. Rawlins, Cecilie F. Rustad, Asbjørg Stray‐Pedersen, Kristian Tveten, Olivia Wenger, Jullianne Diaz, Laura Jenkins, Laura Martin, Marianne McGuire, Marguerite Pietryga, Linda Ramsdell, Leah Slattery, Farida Abid, Alison A. Bertuch, Dorothy K. Grange, LaDonna Immken, Christian P. Schaaf, Hilde Van Esch, Weimin Bi, Sau Wai Cheung, Amy M. Breman, Janice Smith, Chad A. Shaw, Andrew H. Crosby, Christine M. Eng, Yaping Yang, James R. Lupski, Rui Xiao, Pengfei Liu
Έκδοση 2018Artigo -
4
Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders από Madelyn A. Gillentine, Tianyun Wang, Kendra Hoekzema, Jill A. Rosenfeld, Pengfei Liu, Hui Guo, Chang N. Kim, Bert B. A. De Vries, Lisenka E.L.M. Vissers, Magnus Nordenskjöld, Malin Kvarnung, Anna Lindstrand, Ann Nordgren, Jozef Gécz, Maria Iascone, Anna Cereda, Agnese Scatigno, Silvia Maitz, Ginevra Zanni, Enrico Bertini, Christiane Zweier, Sarah Schuhmann, Antje Wiesener, Micah Pepper, Heena Panjwani, Erin Torti, Farida Abid, Irina Anselm, Siddharth Srivastava, Paldeep S. Atwal, Carlos A. Bacino, Gifty Bhat, Katherine Cobian, Lynne M. Bird, Jennifer Friedman, Meredith S. Wright, Bert Callewaert, Florence Petit, Sophie Mathieu, Alexandra Afenjar, Celanie K. Christensen, Kerry White, Orly Elpeleg, Itai Berger, Edward J. Espineli, Christina Fagerberg, Charlotte Brasch‐Andersen, Lars Kjærsgaard Hansen, Timothy Feyma, Susan Hughes, Isabelle Thiffault, Bonnie Sullivan, Shuang Yan, Kory Keller, Boris Keren, Cyril Mignot, R. Frank Kooy, Marije Meuwissen, Alice Basinger, Mary K. Kukolich, Meredith Philips, Lucia Ortega, Margaret Drummond‐Borg, Mathilde Lauridsen, Kristina Sorensen, Anna Lehman, Elena Lopez‐Rangel, Paul A. Levy, Davor Lessel, Timothy Lotze, Suneeta Madan-Khetarpal, Jessica Sebastian, Jodie M. Vento, Divya Vats, L. Manace Benman, Shane McKee, Ghayda Mirzaa, Candace Muss, John Pappas, Hilde Peeters, Corrado Romano, Maurizio Elia, Ornella Galesi, Marleen Simon, Koen L.I. van Gassen, Kara Simpson, Robert F. Stratton, Shakir Syed, Julien Thévenon, Irene Valenzuela, Antonio Vitobello, Marie Bournez, Laurence Faivre, Kun Xia, John Acampado, J. Andrea, Alpha Amatya, Irina Astrovskaya, Asif Bashar, Elizabeth Brooks
Έκδοση 2021Artigo
Εργαλεία αναζήτησης:
Σχετικά θέματα
Biology
Gene
Genetics
Medicine
Allele
Allelic heterogeneity
Bioinformatics
Cancer research
Candidate gene
Cell biology
Chemistry
Computational biology
Copy-number variation
Cornelia de Lange Syndrome
DNA sequencing
Duchenne muscular dystrophy
Dystrophin
Exome
Exome sequencing
Genetic heterogeneity
Genome
Genotype
Human genetics
Indel
Internal medicine
Locus (genetics)
Molecular biology
Muscular dystrophy
Myocyte
Phenotype