Kumar M - Search Results

1

Identification of novel mitochondrial mutations in Leber's hereditary optic neuropathy.

Kumar M, Tanwar M, Saxena R, Sharma P, Dada R. Kumar M, et al. Mol Vis. 2010 Apr 30;16:782-92. Mol Vis. 2010. PMID: 20454697 Free PMC article.

2

Molecular and structural analysis of genetic variations in congenital cataract.

Kumar M, Agarwal T, Kaur P, Kumar M, Khokhar S, Dada R. Kumar M, et al. Mol Vis. 2013 Nov 24;19:2436-50. eCollection 2013. Mol Vis. 2013. PMID: 24319337 Free PMC article.

3

Mutation screening and genotype phenotype correlation of α-crystallin, γ-crystallin and GJA8 gene in congenital cataract.

Kumar M, Agarwal T, Khokhar S, Kumar M, Kaur P, Roy TS, Dada R. Kumar M, et al. Mol Vis. 2011 Mar 11;17:693-707. Mol Vis. 2011. PMID: 21423869 Free PMC article.

4

Clinical characterization and mitochondrial DNA sequence variations in Leber hereditary optic neuropathy.

Kumar M, Kaur P, Kumar M, Saxena R, Sharma P, Dada R. Kumar M, et al. Mol Vis. 2012;18:2687-99. Epub 2012 Nov 12. Mol Vis. 2012. PMID: 23170061 Free PMC article.

5

MYOC and FOXC1 gene analysis in primary congenital glaucoma.

Tanwar M, Kumar M, Dada T, Sihota R, Dada R. Tanwar M, et al. Among authors: kumar m. Mol Vis. 2010 Oct 8;16:1996-2006. Mol Vis. 2010. PMID: 21031026 Free PMC article.

6

VSX1 gene analysis in keratoconus.

Tanwar M, Kumar M, Nayak B, Pathak D, Sharma N, Titiyal JS, Dada R. Tanwar M, et al. Among authors: kumar m. Mol Vis. 2010 Nov 16;16:2395-401. Mol Vis. 2010. PMID: 21139977 Free PMC article.

7

Nucleotide variations in mitochondrial DNA and supra-physiological ROS levels in cytogenetically normal cases of premature ovarian insufficiency.

Kumar M, Pathak D, Kriplani A, Ammini AC, Talwar P, Dada R. Kumar M, et al. Arch Gynecol Obstet. 2010 Dec;282(6):695-705. doi: 10.1007/s00404-010-1623-x. Epub 2010 Aug 1. Arch Gynecol Obstet. 2010. PMID: 20680310

8

Meditation & yoga: Impact on oxidative DNA damage & dysregulated sperm transcripts in male partners of couples with recurrent pregnancy loss.

Dhawan V, Kumar M, Deka D, Malhotra N, Dadhwal V, Singh N, Dada R. Dhawan V, et al. Among authors: kumar m. Indian J Med Res. 2018 Dec;148(Suppl):S134-S139. doi: 10.4103/ijmr.IJMR_1988_17. Indian J Med Res. 2018. PMID: 30964091 Free PMC article.

9

Rieger syndrome with multiple chromosomal breaks and chromosome 4 deletion.

Tanwar M, Kumar R, Goyal A, Kumar M, Dada T, Singh G, Sihota R, Dada R. Tanwar M, et al. Among authors: kumar r, kumar m. BMJ Case Rep. 2009;2009:bcr06.2008.0297. doi: 10.1136/bcr.06.2008.0297. Epub 2009 Feb 16. BMJ Case Rep. 2009. PMID: 21686867 Free PMC article.

10

Association of HLA-G 3'UTR Polymorphisms with Soluble HLA-G Levels and Disease Activity in Patients with Rheumatoid Arthritis: A Case-Control Study.

Gautam S, Kumar U, Kumar M, Kanga U, Dada R. Gautam S, et al. Among authors: kumar u, kumar m. Immunol Invest. 2020 Feb;49(1-2):88-105. doi: 10.1080/08820139.2019.1657146. Epub 2019 Sep 5. Immunol Invest. 2020. PMID: 31549885

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