Pattnaik BR - Search Results

1

Sensing through Non-Sensing Ocular Ion Channels.

Kabra M, Pattnaik BR. Kabra M, et al. Among authors: pattnaik br. Int J Mol Sci. 2020 Sep 21;21(18):6925. doi: 10.3390/ijms21186925. Int J Mol Sci. 2020. PMID: 32967234 Free PMC article. Review.

2

Genetic defects in the hotspot of inwardly rectifying K(+) (Kir) channels and their metabolic consequences: a review.

Pattnaik BR, Asuma MP, Spott R, Pillers DA. Pattnaik BR, et al. Mol Genet Metab. 2012 Jan;105(1):64-72. doi: 10.1016/j.ymgme.2011.10.004. Epub 2011 Oct 19. Mol Genet Metab. 2012. PMID: 22079268 Free PMC article. Review.

3

A Novel KCNJ13 Nonsense Mutation and Loss of Kir7.1 Channel Function Causes Leber Congenital Amaurosis (LCA16).

Pattnaik BR, Shahi PK, Marino MJ, Liu X, York N, Brar S, Chiang J, Pillers DA, Traboulsi EI. Pattnaik BR, et al. Hum Mutat. 2015 Jul;36(7):720-7. doi: 10.1002/humu.22807. Epub 2015 May 20. Hum Mutat. 2015. PMID: 25921210

4

Role of the sigma-1 receptor chaperone in rod and cone photoreceptor degenerations in a mouse model of retinitis pigmentosa.

Yang H, Fu Y, Liu X, Shahi PK, Mavlyutov TA, Li J, Yao A, Guo SZ, Pattnaik BR, Guo LW. Yang H, et al. Among authors: pattnaik br. Mol Neurodegener. 2017 Sep 19;12(1):68. doi: 10.1186/s13024-017-0202-z. Mol Neurodegener. 2017. PMID: 28927431 Free PMC article.

5

Gene Augmentation and Readthrough Rescue Channelopathy in an iPSC-RPE Model of Congenital Blindness.

Shahi PK, Hermans D, Sinha D, Brar S, Moulton H, Stulo S, Borys KD, Capowski E, Pillers DM, Gamm DM, Pattnaik BR. Shahi PK, et al. Among authors: pattnaik br. Am J Hum Genet. 2019 Feb 7;104(2):310-318. doi: 10.1016/j.ajhg.2018.12.019. Epub 2019 Jan 24. Am J Hum Genet. 2019. PMID: 30686507 Free PMC article.

6

Kir7.1 disease mutant T153I within the inner pore affects K⁺ conduction.

Beverley KM, Shahi PK, Kabra M, Zhao Q, Heyrman J, Steffen J, Pattnaik BR. Beverley KM, et al. Among authors: pattnaik br. Am J Physiol Cell Physiol. 2022 Jul 1;323(1):C56-C68. doi: 10.1152/ajpcell.00093.2022. Epub 2022 May 18. Am J Physiol Cell Physiol. 2022. PMID: 35584325 Free PMC article.

7

Nonviral base editing of KCNJ13 mutation preserves vision in a model of inherited retinal channelopathy.

Kabra M, Shahi PK, Wang Y, Sinha D, Spillane A, Newby GA, Saxena S, Tong Y, Chang Y, Abdeen AA, Edwards KL, Theisen CO, Liu DR, Gamm DM, Gong S, Saha K, Pattnaik BR. Kabra M, et al. Among authors: pattnaik br. J Clin Invest. 2023 Oct 2;133(19):e171356. doi: 10.1172/JCI171356. J Clin Invest. 2023. PMID: 37561581 Free PMC article.

8

Transplacental Transfer of Oxytocin and Its Impact on Neonatal Cord Blood and In Vitro Retinal Cell Activity.

Adegboro CO, Luo W, Kabra M, McAdams RM, York NW, Wijenayake RI, Suchla KM, Pillers DM, Pattnaik BR. Adegboro CO, et al. Among authors: pattnaik br. Cells. 2024 Oct 19;13(20):1735. doi: 10.3390/cells13201735. Cells. 2024. PMID: 39451253 Free PMC article.

9

Photoreceptor protection via blockade of BET epigenetic readers in a murine model of inherited retinal degeneration.

Zhao L, Li J, Fu Y, Zhang M, Wang B, Ouellette J, Shahi PK, Pattnaik BR, Watters JJ, Wong WT, Guo LW. Zhao L, et al. Among authors: pattnaik br. J Neuroinflammation. 2017 Jan 19;14(1):14. doi: 10.1186/s12974-016-0775-4. J Neuroinflammation. 2017. PMID: 28103888 Free PMC article.

10

Human iPSC Modeling Reveals Mutation-Specific Responses to Gene Therapy in a Genotypically Diverse Dominant Maculopathy.

Sinha D, Steyer B, Shahi PK, Mueller KP, Valiauga R, Edwards KL, Bacig C, Steltzer SS, Srinivasan S, Abdeen A, Cory E, Periyasamy V, Siahpirani AF, Stone EM, Tucker BA, Roy S, Pattnaik BR, Saha K, Gamm DM. Sinha D, et al. Among authors: pattnaik br. Am J Hum Genet. 2020 Aug 6;107(2):278-292. doi: 10.1016/j.ajhg.2020.06.011. Epub 2020 Jul 23. Am J Hum Genet. 2020. PMID: 32707085 Free PMC article.

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