Juyal RC - Search Results

1

Genetically modified mouse models for the study of nonalcoholic fatty liver disease.

Nagarajan P, Mahesh Kumar MJ, Venkatesan R, Majundar SS, Juyal RC. Nagarajan P, et al. Among authors: juyal rc. World J Gastroenterol. 2012 Mar 21;18(11):1141-53. doi: 10.3748/wjg.v18.i11.1141. World J Gastroenterol. 2012. PMID: 22468076 Free PMC article. Review.

2

Role of immunodeficient animal models in the development of fructose induced NAFLD.

Bhattacharjee J, Kumar JM, Arindkar S, Das B, Pramod U, Juyal RC, Majumdar SS, Nagarajan P. Bhattacharjee J, et al. Among authors: juyal rc. J Nutr Biochem. 2014 Feb;25(2):219-26. doi: 10.1016/j.jnutbio.2013.10.010. Epub 2013 Nov 18. J Nutr Biochem. 2014. PMID: 24445047

3

Antigen peptide transporter 1 is involved in the development of fructose-induced hepatic steatosis in mice.

Arindkar S, Bhattacharjee J, Kumar JM, Das B, Upadhyay P, Asif S, Juyal RC, Majumdar SS, Perumal N. Arindkar S, et al. Among authors: juyal rc. J Gastroenterol Hepatol. 2013 Aug;28(8):1403-9. doi: 10.1111/jgh.12186. J Gastroenterol Hepatol. 2013. PMID: 23488792

4

Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations.

Liu JZ, van Sommeren S, Huang H, Ng SC, Alberts R, Takahashi A, Ripke S, Lee JC, Jostins L, Shah T, Abedian S, Cheon JH, Cho J, Dayani NE, Franke L, Fuyuno Y, Hart A, Juyal RC, Juyal G, Kim WH, Morris AP, Poustchi H, Newman WG, Midha V, Orchard TR, Vahedi H, Sood A, Sung JY, Malekzadeh R, Westra HJ, Yamazaki K, Yang SK; International Multiple Sclerosis Genetics Consortium; International IBD Genetics Consortium; Barrett JC, Alizadeh BZ, Parkes M, Bk T, Daly MJ, Kubo M, Anderson CA, Weersma RK. Liu JZ, et al. Among authors: juyal rc. Nat Genet. 2015 Sep;47(9):979-986. doi: 10.1038/ng.3359. Epub 2015 Jul 20. Nat Genet. 2015. PMID: 26192919 Free PMC article.

5

HLA-DP on Epithelial Cells Enables Tissue Damage by NKp44⁺ Natural Killer Cells in Ulcerative Colitis.

Baumdick ME, Niehrs A, Degenhardt F, Schwerk M, Hinrichs O, Jordan-Paiz A, Padoan B, Wegner LHM, Schloer S, Zecher BF, Malsy J, Joshi VR, Illig C, Schröder-Schwarz J, Möller KJ; Hamburg Intestinal Tissue Study Group; Martin MP, Yuki Y, Ozawa M, Sauter J, Schmidt AH, Perez D, Giannou AD, Carrington M, Davis RS, Schumacher U, Sauter G, Huber S, Puelles VG, Melling N, Franke A; International Inflammatory Bowel Disease Genetics Consortium; Altfeld M, Bunders MJ. Baumdick ME, et al. Gastroenterology. 2023 Oct;165(4):946-962.e13. doi: 10.1053/j.gastro.2023.06.034. Epub 2023 Jul 15. Gastroenterology. 2023. PMID: 37454979 Free article.

6

Stratification of rheumatoid arthritis cohort using Ayurveda based deep phenotyping approach identifies novel genes in a GWAS.

Juyal G, Pandey A, Garcia SL, Negi S, Gupta R, Kumar U, Bhat B, Juyal RC, Thelma BK. Juyal G, et al. Among authors: juyal rc. J Ayurveda Integr Med. 2022 Jul-Sep;13(3):100578. doi: 10.1016/j.jaim.2022.100578. Epub 2022 Jul 3. J Ayurveda Integr Med. 2022. PMID: 35793592 Free PMC article.

7

Compound heterozygous variants in Wiskott-Aldrich syndrome like (WASL) gene segregating in a family with early onset Parkinson's disease.

Kumar S, Abbas MM, Govindappa ST, Muthane UB, Behari M, Pandey S, Juyal RC, Thelma BK. Kumar S, et al. Among authors: juyal rc. Parkinsonism Relat Disord. 2021 Mar;84:61-67. doi: 10.1016/j.parkreldis.2021.02.001. Epub 2021 Feb 5. Parkinsonism Relat Disord. 2021. PMID: 33571872

8

Early Onset Parkinson's disease due to DJ1 mutations: An Indian study.

Abbas MM, Govindappa ST, Sudhaman S, Thelma BK, Juyal RC, Behari M, Muthane UB. Abbas MM, et al. Among authors: juyal rc. Parkinsonism Relat Disord. 2016 Nov;32:20-24. doi: 10.1016/j.parkreldis.2016.04.024. Epub 2016 Apr 24. Parkinsonism Relat Disord. 2016. PMID: 27592010

9

Evidence of mutations in RIC3 acetylcholine receptor chaperone as a novel cause of autosomal-dominant Parkinson's disease with non-motor phenotypes.

Sudhaman S, Muthane UB, Behari M, Govindappa ST, Juyal RC, Thelma BK. Sudhaman S, et al. Among authors: juyal rc. J Med Genet. 2016 Aug;53(8):559-66. doi: 10.1136/jmedgenet-2015-103616. Epub 2016 Apr 7. J Med Genet. 2016. PMID: 27055476

10

Discovery of a frameshift mutation in podocalyxin-like (PODXL) gene, coding for a neural adhesion molecule, as causal for autosomal-recessive juvenile Parkinsonism.

Sudhaman S, Prasad K, Behari M, Muthane UB, Juyal RC, Thelma BK. Sudhaman S, et al. Among authors: juyal rc. J Med Genet. 2016 Jul;53(7):450-6. doi: 10.1136/jmedgenet-2015-103459. Epub 2016 Feb 10. J Med Genet. 2016. PMID: 26864383

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