Ray K - Search Results

1

Analysis of Wilson disease mutations revealed that interactions between different ATP7B mutants modify their properties.

Roy S, McCann CJ, Ralle M, Ray K, Ray J, Lutsenko S, Jayakanthan S. Roy S, et al. Among authors: ray j, ray k. Sci Rep. 2020 Aug 10;10(1):13487. doi: 10.1038/s41598-020-70366-7. Sci Rep. 2020. PMID: 32778786 Free PMC article.

2

Influence of Apolipoprotein E polymorphism on susceptibility of Wilson disease.

Roy S, Ganguly K, Pal P, Ghosh S, Das SK, Gangopadhyay PK, Bavdekar A, Ray K, Sengupta M, Ray J. Roy S, et al. Among authors: ray j, ray k. Ann Hum Genet. 2018 Mar;82(2):53-59. doi: 10.1111/ahg.12223. Epub 2017 Oct 23. Ann Hum Genet. 2018. PMID: 29059476

3

Potential Role of Brain-Derived Neurotrophic Factor and Dopamine Receptor D2 Gene Variants as Modifiers for the Susceptibility and Clinical Course of Wilson's Disease.

Roy S, Pal P, Ghosh S, Bhattacharya S, Das SK, Gangopadhyay PK, Bavdekar A, Ray K, Sengupta M, Ray J. Roy S, et al. Among authors: ray j, ray k. Neuromolecular Med. 2018 Sep;20(3):401-408. doi: 10.1007/s12017-018-8501-2. Epub 2018 Jul 10. Neuromolecular Med. 2018. PMID: 29992511

4

Dopamine β hydroxylase (DBH) polymorphisms do not contribute towards the clinical course of Wilson's disease in Indian patients.

Roy S, Ghosh S, Bhattacharya S, Saha A, Das SK, Gangopadhyay PK, Bavdekar A, Ray K, Sengupta M, Ray J. Roy S, et al. Among authors: ray j, ray k. J Gene Med. 2019 Sep;21(9):e3109. doi: 10.1002/jgm.3109. Epub 2019 Jul 23. J Gene Med. 2019. PMID: 31265749

5

Evaluation of genetic association of the INK4 locus with primary open angle glaucoma in East Indian population.

Vishal M, Sharma A, Kaurani L, Chakraborty S, Ray J, Sen A, Mukhopadhyay A, Ray K. Vishal M, et al. Among authors: ray j, ray k. Sci Rep. 2014 May 30;4:5115. doi: 10.1038/srep05115. Sci Rep. 2014. PMID: 24875940 Free PMC article.

6

Association of TOR1A and GCH1 Polymorphisms with Isolated Dystonia in India.

Giri S, Ghosh A, Roy S, Sankhla CS, Das SK, Ray K, Ray J. Giri S, et al. Among authors: ray j, ray k. J Mol Neurosci. 2021 Feb;71(2):325-337. doi: 10.1007/s12031-020-01653-1. Epub 2020 Jul 13. J Mol Neurosci. 2021. PMID: 32662044

7

A Compound Heterozygote for GCH1 Mutation Represents a Case of Atypical Dopa-Responsive Dystonia.

Giri S, Naiya T, Roy S, Das G, Wali GM, Das SK, Ray K, Ray J. Giri S, et al. Among authors: ray j, ray k. J Mol Neurosci. 2019 Jun;68(2):214-220. doi: 10.1007/s12031-019-01301-3. Epub 2019 Mar 25. J Mol Neurosci. 2019. PMID: 30911941

8

Molecular pathogenesis of Wilson disease: haplotype analysis, detection of prevalent mutations and genotype-phenotype correlation in Indian patients.

Gupta A, Aikath D, Neogi R, Datta S, Basu K, Maity B, Trivedi R, Ray J, Das SK, Gangopadhyay PK, Ray K. Gupta A, et al. Among authors: ray j, ray k. Hum Genet. 2005 Oct;118(1):49-57. doi: 10.1007/s00439-005-0007-y. Epub 2005 Oct 28. Hum Genet. 2005. PMID: 16133174

9

Molecular pathogenesis of Parkinson's disease: identification of mutations in the Parkin gene in Indian patients.

Biswas A, Gupta A, Naiya T, Das G, Neogi R, Datta S, Mukherjee S, Das SK, Ray K, Ray J. Biswas A, et al. Among authors: ray j, ray k. Parkinsonism Relat Disord. 2006 Oct;12(7):420-6. doi: 10.1016/j.parkreldis.2006.04.005. Epub 2006 Jun 21. Parkinsonism Relat Disord. 2006. PMID: 16793319

10

Microtubule-associated protein tau (MAPT) influences the risk of Parkinson's disease among Indians.

Das G, Misra AK, Das SK, Ray K, Ray J. Das G, et al. Among authors: ray j, ray k. Neurosci Lett. 2009 Aug 21;460(1):16-20. doi: 10.1016/j.neulet.2009.05.031. Epub 2009 May 18. Neurosci Lett. 2009. PMID: 19450659

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