| Year |
Citation |
Score |
| 2017 |
Katikireddy KR, White TL, Miyajima T, Vasanth S, Raoof D, Chen Y, Price MO, Price FW, Jurkunas UV. NQO1 downregulation potentiates menadione-induced endothelial-mesenchymal transition during rosette formation in Fuchs endothelial corneal dystrophy. Free Radical Biology & Medicine. PMID 29294389 DOI: 10.1016/J.Freeradbiomed.2017.12.036 |
0.343 |
|
| 2016 |
Khan SY, Vasanth S, Kabir F, Gottsch JD, Khan AO, Chaerkady R, Lee MW, Leitch CC, Ma Z, Laux J, Villasmil R, Khan SN, Riazuddin S, Akram J, Cole RN, et al. FOXE3 contributes to Peters anomaly through transcriptional regulation of an autophagy-associated protein termed DNAJB1. Nature Communications. 7: 10953. PMID 27218149 DOI: 10.1038/Ncomms10953 |
0.398 |
|
| 2012 |
Lichti-Kaiser K, ZeRuth G, Kang HS, Vasanth S, Jetten AM. Gli-similar proteins: their mechanisms of action, physiological functions, and roles in disease. Vitamins and Hormones. 88: 141-71. PMID 22391303 DOI: 10.1016/B978-0-12-394622-5.00007-9 |
0.455 |
|
| 2011 |
Talbot JJ, Shillingford JM, Vasanth S, Doerr N, Mukherjee S, Kinter MT, Watnick T, Weimbs T. Polycystin-1 regulates STAT activity by a dual mechanism. Proceedings of the National Academy of Sciences of the United States of America. 108: 7985-90. PMID 21518865 DOI: 10.1073/Pnas.1103816108 |
0.441 |
|
| 2011 |
Vasanth S, ZeRuth G, Kang HS, Jetten AM. Identification of nuclear localization, DNA binding, and transactivating mechanisms of Kruppel-like zinc finger protein Gli-similar 2 (Glis2). The Journal of Biological Chemistry. 286: 4749-59. PMID 21127075 DOI: 10.1074/Jbc.M110.165951 |
0.497 |
|
| 2010 |
Kang HS, ZeRuth G, Lichti-Kaiser K, Vasanth S, Yin Z, Kim YS, Jetten AM. Gli-similar (Glis) Krüppel-like zinc finger proteins: insights into their physiological functions and critical roles in neonatal diabetes and cystic renal disease. Histology and Histopathology. 25: 1481-96. PMID 20865670 DOI: 10.14670/Hh-25.1481 |
0.579 |
|
| 2006 |
Low SH, Vasanth S, Larson CH, Mukherjee S, Sharma N, Kinter MT, Kane ME, Obara T, Weimbs T. Polycystin-1, STAT6, and P100 function in a pathway that transduces ciliary mechanosensation and is activated in polycystic kidney disease. Developmental Cell. 10: 57-69. PMID 16399078 DOI: 10.1016/J.Devcel.2005.12.005 |
0.654 |
|
| Low-probability matches (unlikely to be authored by this person) |
| 2013 |
Riazuddin SA, Vasanth S, Katsanis N, Gottsch JD. Mutations in AGBL1 cause dominant late-onset Fuchs corneal dystrophy and alter protein-protein interaction with TCF4. American Journal of Human Genetics. 93: 758-64. PMID 24094747 DOI: 10.1016/J.Ajhg.2013.08.010 |
0.296 |
|
| 2018 |
Eghrari AO, Vasanth S, Gapsis BC, Bison H, Jurkunas U, Riazuddin SA, Gottsch JD. Identification of a Novel TCF4 Isoform in the Human Corneal Endothelium. Cornea. PMID 29677003 DOI: 10.1097/Ico.0000000000001521 |
0.295 |
|
| 2014 |
Carvalho CM, Vasanth S, Shinawi M, Russell C, Ramocki MB, Brown CW, Graakjaer J, Skytte AB, Vianna-Morgante AM, Krepischi AC, Patel GS, Immken L, Aleck K, Lim C, Cheung SW, et al. Dosage changes of a segment at 17p13.1 lead to intellectual disability and microcephaly as a result of complex genetic interaction of multiple genes. American Journal of Human Genetics. 95: 565-78. PMID 25439725 DOI: 10.1016/J.Ajhg.2014.10.006 |
0.294 |
|
| 2019 |
Miyai T, Vasanth S, Melangath G, Deshpande N, Kumar V, Benischke AS, Chen Y, Price MO, Price FW, Jurkunas UV. Activation of PINK1-Parkin-Mediated Mitophagy Degrades Mitochondrial Quality Control Proteins in Fuchs Endothelial Corneal Dystrophy. The American Journal of Pathology. PMID 31361992 DOI: 10.1016/J.Ajpath.2019.06.012 |
0.284 |
|
| 2019 |
Miyajima T, Melangath G, Zhu S, Deshpande N, Vasanth S, Mondal B, Kumar V, Chen Y, Price M, Price F, Rogan EG, Zahid M, Jurkunas U. Loss of NQO1 generates genotoxic estrogen-DNA adducts in Fuchs Endothelial Corneal Dystrophy. Free Radical Biology & Medicine. PMID 31857234 DOI: 10.1016/J.Freeradbiomed.2019.12.014 |
0.28 |
|
| 2017 |
Benischke AS, Vasanth S, Miyai T, Katikireddy KR, White T, Chen Y, Halilovic A, Price M, Price F, Liton PB, Jurkunas UV. Activation of mitophagy leads to decline in Mfn2 and loss of mitochondrial mass in Fuchs endothelial corneal dystrophy. Scientific Reports. 7: 6656. PMID 28751712 DOI: 10.1038/S41598-017-06523-2 |
0.277 |
|
| 2019 |
Liu C, Miyajima T, Melangath G, Miyai T, Vasanth S, Deshpande N, Kumar V, Ong Tone S, Gupta R, Zhu S, Vojnovic D, Chen Y, Rogan EG, Mondal B, Zahid M, et al. Ultraviolet A light induces DNA damage and estrogen-DNA adducts in Fuchs endothelial corneal dystrophy causing females to be more affected. Proceedings of the National Academy of Sciences of the United States of America. PMID 31852820 DOI: 10.1073/Pnas.1912546116 |
0.274 |
|
| 2015 |
Oh EC, Vasanth S, Katsanis N. Metabolic regulation and energy homeostasis through the primary Cilium. Cell Metabolism. 21: 21-31. PMID 25543293 DOI: 10.1016/J.Cmet.2014.11.019 |
0.258 |
|
| 2018 |
Ali M, Khan SY, Vasanth S, Ahmed MR, Chen R, Na CH, Thomson JJ, Qiu C, Gottsch JD, Riazuddin SA. Generation and Proteome Profiling of PBMC-Originated, iPSC-Derived Corneal Endothelial Cells. Investigative Ophthalmology & Visual Science. 59: 2437-2444. PMID 29847650 DOI: 10.1167/Iovs.17-22927 |
0.238 |
|
| 2016 |
Eghrari AO, Vasanth S, Wang J, Vahedi F, Riazuddin SA, Gottsch JD. CTG18.1 Expansion in TCF4 Increases Likelihood of Transplantation in Fuchs Corneal Dystrophy. Cornea. PMID 27755191 DOI: 10.1097/Ico.0000000000001049 |
0.238 |
|
| 2015 |
Vasanth S, Eghrari AO, Gapsis BC, Wang J, Haller NF, Stark WJ, Katsanis N, Riazuddin SA, Gottsch JD. Expansion of CTG18.1 Trinucleotide Repeat in TCF4 Is a Potent Driver of Fuchs' Corneal Dystrophy. Investigative Ophthalmology & Visual Science. 56: 4531-6. PMID 26200491 DOI: 10.1167/Iovs.14-16122 |
0.194 |
|
| 2023 |
Ashraf S, Deshpande N, Vasanth S, Melangath G, Wong RJ, Zhao Y, Price M, Price F, Jurkunas UV. Dysregulation of DNA repair genes in Fuchs endothelial corneal dystrophy. Experimental Eye Research. 109499. PMID 37169279 DOI: 10.1016/j.exer.2023.109499 |
0.15 |
|
| Hide low-probability matches. |