M. Kabra

发表

Detection of pregnancy and fertility status in big cats using an enzyme immunoassay based on 5α-pregnan-3α-ol-20-one.

S. Shivaji, Wasimuddin, Vinod Kumar, 2013, General and comparative endocrinology.

Angiopoietin receptor TEK interacts with CYP1B1 in primary congenital glaucoma

Sonika C. Rathi, H. Khanna, R. Khanna, 2017, Human Genetics.

Sensing through Non-Sensing Ocular Ion Channels

B. Pattnaik, M. Kabra, 2020, International journal of molecular sciences.

Genotype-Phenotype Correlations in CYP1B1-Associated Primary Congenital Glaucoma Patients Representing Two Large Cohorts from India and Brazil

V. P. Costa, M. B. de Melo, S. Senthil, 2015, PloS one.

Comprehensive Analysis of CRISPR Base Editing Outcomes for Multimeric Protein

David R. Liu, Gregory A. Newby, Krishanu Saha, 2022, bioRxiv.

Loss of PRSS56 function leads to ocular angle defects and increased susceptibility to high intraocular pressure

R. Khanna, S. John, S. Senthil, 2020, Disease Models & Mechanisms.

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

Qianqian Zhao, P. Shahi, B. Pattnaik, 2022, American journal of physiology. Cell physiology.

Nanoparticle mediated in vitro and in vivo CRISPR base correction of LCA16 causing nonsense mutation rescues Kir7.1 channel function

David R. Liu, Krishanu Saha, Yuyuan Wang, 2022 .

Nanoparticle mediated CRISPR base editing rescues Kir7.1 function relevant to ocular channelopathy

Gregory A. Newby, Krishanu Saha, Yuyuan Wang, 2022 .

Loss of PRSS56 function leads to ocular angle defects and increased susceptibility to high intraocular pressure.

R. Khanna, S. John, S. Senthil, 2020, Disease models & mechanisms.

Peters Anomaly in Nail-Patella Syndrome: A Case Report and Clinico-Genetic Correlation

S. Chaurasia, S. Chakrabarti, D. Edward, 2021, Cornea.

Nonviral base editing of KCNJ13 mutation preserves vision in an inherited retinal channelopathy

Gregory A. Newby, Krishanu Saha, Yuyuan Wang, 2023, bioRxiv.