PubMed ID: 27863209 Author(s): Lee WH, Higuchi H, Ikeda S, Macke EL, Takimoto T, Pattnaik BR, Liu C, Chu LF, Siepka SM, Krentz KJ, Rubinstein CD, Kalejta RF, Thomson JA, Mullins RF, Takahashi JS, Pinto …
Bikash Pattnaik
High glucose promotes the migration of retinal pigment epithelial cells through increased oxidative stress and PEDF expression.
PubMed ID: 27440660 Author(s): Farnoodian M, Halbach C, Slinger C, Pattnaik BR, Sorenson CM, Sheibani N. High glucose promotes the migration of retinal pigment epithelial cells through increased oxidative stress and PEDF expression. Am J …
Cell line donor genotype and its influence on experimental phenotype: Toll-like receptor SNPs and potential variability in innate immunity.
PubMed ID: 27324283 Author(s): Tokarz SA, DeValk J, Luo W, Pattnaik BR, Schrodi SJ, Pillers DA. Cell line donor genotype and its influence on experimental phenotype: Toll-like receptor SNPs and potential variability in innate immunity. …
Inhibition of mitochondrial β-oxidation by miR-107 promotes hepatic lipid accumulation and impairs glucose tolerance in vivo.
PubMed ID: 26499439 Author(s): Bhatia H, Pattnaik BR, Datta M. Inhibition of mitochondrial β-oxidation by miR-107 promotes hepatic lipid accumulation and impairs glucose tolerance in vivo. Int J Obes (Lond). 2016 May;40(5):861-9. doi: 10.1038/ijo.2015.225. Epub …
A Novel KCNJ13 Nonsense Mutation and Loss of Kir7.1 Channel Function Causes Leber Congenital Amaurosis (LCA16).
PubMed ID: 25921210 Author(s): Pattnaik BR, Shahi PK, Marino MJ, Liu X, York N, Brar S, Chiang J, Pillers DA, Traboulsi EI. A novel KCNJ13 nonsense mutation and loss of Kir7.1 channel function causes Leber …
Oxytocin expression and function in the posterior retina: a novel signaling pathway.
PubMed ID: 25593022 Author(s): Halbach P, Pillers DA, York N, Asuma MP, Chiu MA, Luo W, Tokarz S, Bird IM, Pattnaik BR. Oxytocin expression and function in the posterior retina: a novel signaling pathway. Invest …
Focus on Kir7.1: physiology and channelopathy.
PubMed ID: 25558901 Author(s): Kumar M, Pattnaik BR. Focus on Kir7.1: physiology and channelopathy. Channels (Austin). 2014;8(6):488-95. doi: 10.4161/19336950.2014.959809. Review. PMID 25558901 Journal: Channels (Austin, Tex.), Volume 8, Issue 6, 2014 Genetic studies have linked …
iPS cell modeling of Best disease: insights into the pathophysiology of an inherited macular degeneration.
PubMed ID: 23139242 Author(s): Singh R, Shen W, Kuai D, Martin JM, Guo X, Smith MA, Perez ET, Phillips MJ, Simonett JM, Wallace KA, Verhoeven AD, Capowski EE, Zhang X, Yin Y, Halbach PJ, Fishman …
Snowflake vitreoretinal degeneration (SVD) mutation R162W provides new insights into Kir7.1 ion channel structure and function.
PubMed ID: 23977131 Author(s): Pattnaik BR, Tokarz S, Asuma MP, Schroeder T, Sharma A, Mitchell JC, Edwards AO, Pillers DA. Snowflake vitreoretinal degeneration (SVD) mutation R162W provides new insights into Kir7.1 ion channel structure and …