Metabolic regulation and energy homeostasis through the primary cilium

Bằng Oh, Edwin C., Vasanth, Shivakumar, Katsanis, Nicholas
Xuất bản năm Cell Metab (2014)

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

Bằng Riazuddin, S. Amer, Vasanth, Shivakumar, Katsanis, Nicholas, Gottsch, John D.
Được phát hành 2013

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

Bằng Vasanth, Shivakumar, ZeRuth, Gary, Kang, Hong Soon, Jetten, Anton M.
Được phát hành 2011

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

Bằng Lichti-Kaiser, Kristin, ZeRuth, Gary, Kang, Hong Soon, Vasanth, Shivakumar, Jetten, Anton M.
Được phát hành 2012

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

Bằng Eghrari, Allen O., Vasanth, Shivakumar, Wang, Jiangxia, Vahedi, Farnoosh, Riazuddin, S. Amer, Gottsch, John D.
Xuất bản năm Cornea (2017)

Identification of a novel TCF4 isoform in human corneal endothelium

Bằng Eghrari, Allen O., Vasanth, Shivakumar, Gapsis, Briana C., Bison, Henry, Jurkunas, Ula, Riazuddin, S. Amer, Gottsch, John D.
Xuất bản năm Cornea (2018)

Polycystin-1 regulates STAT activity by a dual mechanism

Bằng Talbot, Jeffrey J., Shillingford, Jonathan M., Vasanth, Shivakumar, Doerr, Nicholas, Mukherjee, Sambuddho, Kinter, Mike T., Watnick, Terry, Weimbs, Thomas
Được phát hành 2011

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

Bằng Kang, Hong Soon, ZeRuth, Gary, Lichti-Kaiser, Kristin, Vasanth, Shivakumar, Yin, Zhengyu, Kim, Yong-Sik, Jetten, Anton M.
Được phát hành 2010

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

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

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

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

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

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

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

Bằng 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
Xuất bản năm Invest Ophthalmol Vis Sci (2018)

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

Bằng 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.
Xuất bản năm Sci Rep (2017)

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

Bằng 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
Xuất bản năm 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

Bằng 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.
Xuất bản năm 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

Bằng 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.
Xuất bản năm Am J Hum Genet (2014)

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

Bằng 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
Xuất bản năm Nat Commun (2016)