Metabolic regulation and energy homeostasis through the primary cilium

Autor Oh, Edwin C., Vasanth, Shivakumar, Katsanis, Nicholas
Vydáno v Cell Metab (2014)

Mutations in AGBL1 Cause Dominant Late-Onset Fuchs Corneal Dystrophy and Alter Protein-Protein Interaction with TCF4

Autor Riazuddin, S. Amer, Vasanth, Shivakumar, Katsanis, Nicholas, Gottsch, John D.
Vydáno 2013

Identification of Nuclear Localization, DNA Binding, and Transactivating Mechanisms of Krüppel-like Zinc Finger Protein Gli-Similar 2 (Glis2)

Autor Vasanth, Shivakumar, ZeRuth, Gary, Kang, Hong Soon, Jetten, Anton M.
Vydáno 2011

Gli-Similar (Glis) Proteins: Their Mechanisms of Action, Physiological Functions, and Roles in Disease

Autor Lichti-Kaiser, Kristin, ZeRuth, Gary, Kang, Hong Soon, Vasanth, Shivakumar, Jetten, Anton M.
Vydáno 2012

CTG18.1 Expansion in TCF4 increases likelihood of transplantation in Fuchs Corneal Dystrophy

Autor Eghrari, Allen O., Vasanth, Shivakumar, Wang, Jiangxia, Vahedi, Farnoosh, Riazuddin, S. Amer, Gottsch, John D.
Vydáno v Cornea (2017)

Identification of a novel TCF4 isoform in human corneal endothelium

Autor Eghrari, Allen O., Vasanth, Shivakumar, Gapsis, Briana C., Bison, Henry, Jurkunas, Ula, Riazuddin, S. Amer, Gottsch, John D.
Vydáno v Cornea (2018)

Polycystin-1 regulates STAT activity by a dual mechanism

Autor Talbot, Jeffrey J., Shillingford, Jonathan M., Vasanth, Shivakumar, Doerr, Nicholas, Mukherjee, Sambuddho, Kinter, Mike T., Watnick, Terry, Weimbs, Thomas
Vydáno 2011

Gli-similar (Glis) Krüppel-like zinc finger proteins: insights into their physiological functions and critical roles in neonatal diabetes and cystic renal disease

Autor Kang, Hong Soon, ZeRuth, Gary, Lichti-Kaiser, Kristin, Vasanth, Shivakumar, Yin, Zhengyu, Kim, Yong-Sik, Jetten, Anton M.
Vydáno 2010

Expansion of CTG18.1 Trinucleotide Repeat in TCF4 Is a Potent Driver of Fuchs' Corneal Dystrophy

Autor Vasanth, Shivakumar, Eghrari, Allen O., Gapsis, Briana C., Wang, Jiangxia, Haller, Nicolas F., Stark, Walter J., Katsanis, Nicholas, Riazuddin, S. Amer, Gottsch, John D.
Vydáno v Invest Ophthalmol Vis Sci (2015)

NQO1 downregulation potentiates menadione-induced endothelial-mesenchymal transition during rosette formation in Fuchs endothelial corneal dystrophy

Autor Katikireddy, Kishore Reddy, White, Tomas L., Miyajima, Taiga, Vasanth, Shivakumar, Raoof, Duna, Chen, Yuming, Price, Marianne O., Price, Francis W., Jurkunas, Ula V.
Vydáno v Free Radic Biol Med (2017)

Activation of PINK1-Parkin–Mediated Mitophagy Degrades Mitochondrial Quality Control Proteins in Fuchs Endothelial Corneal Dystrophy

Autor Miyai, Takashi, Vasanth, Shivakumar, Melangath, Geetha, Deshpande, Neha, Kumar, Varun, Benischke, Anne-Sophie, Chen, Yuming, Price, Marianne O., Price, Francis W., Jurkunas, Ula V.
Vydáno v Am J Pathol (2019)

Generation and Proteome Profiling of PBMC-Originated, iPSC-Derived Corneal Endothelial Cells

Autor Ali, Muhammad, Khan, Shahid Y., Vasanth, Shivakumar, Ahmed, Mariya R., Chen, Ruiqiang, Na, Chan Hyun, Thomson, Jason J., Qiu, Caihong, Gottsch, John D., Riazuddin, S. Amer
Vydáno v Invest Ophthalmol Vis Sci (2018)

Activation of mitophagy leads to decline in Mfn2 and loss of mitochondrial mass in Fuchs endothelial corneal dystrophy

Autor Benischke, Anne-Sophie, Vasanth, Shivakumar, Miyai, Takashi, Katikireddy, Kishore Reddy, White, Tomas, Chen, Yuming, Halilovic, Adna, Price, Marianne, Price, Francis, Liton, Paloma B., Jurkunas, Ula V.
Vydáno v Sci Rep (2017)

Loss of NQO1 generates genotoxic estrogen-DNA adducts in Fuchs Endothelial Corneal Dystrophy

Autor Miyajima, Taiga, Melangath, Geetha, Zhu, Shan, Deshpande, Neha, Vasanth, Shivakumar, Mondal, Bodhisattwa, Kumar, Varun, Chen, Yuming, Price, Marianne, Price, Francis, Rogan, Eleanor G., Zahid, Muhammad, Jurkunas, Ula
Vydáno v Free Radic Biol Med (2019)

Ultraviolet A light induces DNA damage and estrogen-DNA adducts in Fuchs endothelial corneal dystrophy causing females to be more affected

Autor Liu, Cailing, Miyajima, Taiga, Melangath, Geetha, Miyai, Takashi, Vasanth, Shivakumar, Deshpande, Neha, Kumar, Varun, Ong Tone, Stephan, Gupta, Reena, Zhu, Shan, Vojnovic, Dijana, Chen, Yuming, Rogan, Eleanor G., Mondal, Bodhiswatta, Zahid, Muhammad, Jurkunas, Ula V.
Vydáno v Proc Natl Acad Sci U S A (2020)

Dosage Changes of a Segment at 17p13.1 Lead to Intellectual Disability and Microcephaly as a Result of Complex Genetic Interaction of Multiple Genes

Autor Carvalho, Claudia M.B., Vasanth, Shivakumar, Shinawi, Marwan, Russell, Chad, Ramocki, Melissa B., Brown, Chester W., Graakjaer, Jesper, Skytte, Anne-Bine, Vianna-Morgante, Angela M., Krepischi, Ana C.V., Patel, Gayle S., Immken, LaDonna, Aleck, Kyrieckos, Lim, Cynthia, Cheung, Sau Wai, Rosenberg, Carla, Katsanis, Nicholas, Lupski, James R.
Vydáno v Am J Hum Genet (2014)

FOXE3 contributes to Peters anomaly through transcriptional regulation of an autophagy-associated protein termed DNAJB1

Autor Khan, Shahid Y., Vasanth, Shivakumar, Kabir, Firoz, Gottsch, John D., Khan, Arif O., Chaerkady, Raghothama, Lee, Mei-Chong W., Leitch, Carmen C., Ma, Zhiwei, Laux, Julie, Villasmil, Rafael, Khan, Shaheen N., Riazuddin, Sheikh, Akram, Javed, Cole, Robert N., Talbot, C. Conover, Pourmand, Nader, Zaghloul, Norann A., Hejtmancik, J. Fielding, Riazuddin, S. Amer
Vydáno v Nat Commun (2016)