檢索結果 - V. Vinod Mootha
- Showing 1 - 9 results of 9
-
1
-
2
-
3
-
4
-
5
Transethnic Replication of Association of CTG18.1 Repeat Expansion of<i>TCF4</i>Gene With Fuchs' Corneal Dystrophy in Chinese Implies Common Causal Variant 由 Chao Xing, Xin Gong, Imran Hussain, Chiea Chuen Khor, Donald Tan, Tin Aung, Jodhbir S. Mehta, Eranga N. Vithana, V. Vinod Mootha
出版 2014Artigo -
6
-
7
-
8
Analyzing pre-symptomatic tissue to gain insights into the molecular and mechanistic origins of late-onset degenerative trinucleotide repeat disease 由 Yongjun Chu, Jiaxin Hu, Hanquan Liang, Mohammed Kanchwala, Chao Xing, Walter E. Beebe, C. Bradley Bowman, Xin Gong, David R. Corey, V. Vinod Mootha
出版 2020Artigo -
9
Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy 由 Natalie A. Afshari, Robert P. Igo, Nathan Morris, Dwight Stambolian, Shiwani Sharma, V. Lakshmi Pulagam, Steven P. Dunn, J. Stamler, Barbara Truitt, Jacqueline Rimmler, Abraham Kuot, Christopher R. Croasdale, Xuejun Qin, Kathryn P. Burdon, Sheikh Riazuddin, Richard Mills, Sonja Klebe, Mollie Minear, Jiagang Zhao, Elmer Balajonda, George O. D. Rosenwasser, Keith H. Baratz, V. Vinod Mootha, Sanjay V. Patel, Simon G. Gregory, Joan E. Bailey‐Wilson, Marianne O. Price, Francis W. Price, Jamie E. Craig, John H. Fingert, John D. Gottsch, Anthony J. Aldave, Gordon K. Klintworth, Jonathan H. Lass, Yi‐Ju Li, Sudha K. Iyengar
出版 2017Artigo
相關主題
Biology
Genetics
Gene
Medicine
Allele
Trinucleotide repeat expansion
Cornea
Corneal dystrophy
Ophthalmology
Pathology
RNA
Genotype
Internal medicine
Molecular biology
Neuroscience
RNA splicing
Single-nucleotide polymorphism
Alternative splicing
Antisense RNA
Bioinformatics
Cancer research
Cell biology
Chemistry
Corneal endothelium
DNA sequencing
Diabetes mellitus
Disease
Endocrinology
Endothelium
Enhancer