Metabolic regulation and energy homeostasis through the primary cilium

بواسطة Oh, Edwin C., Vasanth, Shivakumar, Katsanis, Nicholas
الحاوية / القاعدة Cell Metab (2014)

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

بواسطة Riazuddin, S. Amer, Vasanth, Shivakumar, Katsanis, Nicholas, Gottsch, John D.
منشور في 2013

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

بواسطة Vasanth, Shivakumar, ZeRuth, Gary, Kang, Hong Soon, Jetten, Anton M.
منشور في 2011

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

بواسطة Lichti-Kaiser, Kristin, ZeRuth, Gary, Kang, Hong Soon, Vasanth, Shivakumar, Jetten, Anton M.
منشور في 2012

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

بواسطة Eghrari, Allen O., Vasanth, Shivakumar, Wang, Jiangxia, Vahedi, Farnoosh, Riazuddin, S. Amer, Gottsch, John D.
الحاوية / القاعدة Cornea (2017)

Identification of a novel TCF4 isoform in human corneal endothelium

بواسطة Eghrari, Allen O., Vasanth, Shivakumar, Gapsis, Briana C., Bison, Henry, Jurkunas, Ula, Riazuddin, S. Amer, Gottsch, John D.
الحاوية / القاعدة Cornea (2018)

Polycystin-1 regulates STAT activity by a dual mechanism

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

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

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

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

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

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

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

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

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

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

بواسطة 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
الحاوية / القاعدة Invest Ophthalmol Vis Sci (2018)

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

بواسطة 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.
الحاوية / القاعدة Sci Rep (2017)

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

بواسطة 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
الحاوية / القاعدة 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

بواسطة 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.
الحاوية / القاعدة 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

بواسطة 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.
الحاوية / القاعدة Am J Hum Genet (2014)

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

بواسطة 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
الحاوية / القاعدة Nat Commun (2016)