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Novel PANK2 Variant in Asian Indians with Atypical Pantothenate Kinase Associated Neurodegeneration.
Saini A, Holla VV, Kalikavil Puthanveedu D, Mehta S, Elavarasi A, Pillai KS, Mohapatra P, Kumari R, Bari S, Singh I, Cherian A, Krishnan S, Radhakrishnan DM, Agarwal A, Garg D, Garg K, Singh M, Garg A, Muthusamy B, Lal V, Kishore A, Pal PK, Srivastava A, Faruq M, Rajan R. Saini A, et al. Among authors: faruq m. Mov Disord. 2024 May;39(5):920-923. doi: 10.1002/mds.29737. Epub 2024 Mar 20. Mov Disord. 2024. PMID: 38506547 No abstract available.
Spectrum of Alport syndrome in an Indian cohort.
Yadav M, Jadon T, Singh G, Devi KG, Chandan M, Khandelwal P, Meena J, Geetha TS, Faruq M, Hari P, Sinha A, Bagga A. Yadav M, et al. Among authors: faruq m. Pediatr Nephrol. 2025 Feb;40(2):393-405. doi: 10.1007/s00467-024-06507-1. Epub 2024 Sep 16. Pediatr Nephrol. 2025. PMID: 39278986
Anastrozole-mediated modulation of mitochondrial activity by inhibition of mitochondrial permeability transition pore opening: an initial perspective.
Kumar S, Choudhary N, Faruq M, Kumar A, Saran RK, Indercanti PK, Singh V, Sait H, Jaitley S, Valis M, Kuca K, Polipalli SK, Kumar M, Singh T, Suravajhala P, Sharma R, Kapoor S. Kumar S, et al. Among authors: faruq m. J Biomol Struct Dyn. 2023;41(23):14063-14079. doi: 10.1080/07391102.2023.2176927. Epub 2023 Feb 23. J Biomol Struct Dyn. 2023. PMID: 36815262
Whole exome sequencing in an Indian family links Coats plus syndrome and dextrocardia with a homozygous novel CTC1 and a rare HES7 variation.
Netravathi M, Kumari R, Kapoor S, Dakle P, Dwivedi MK, Roy SD, Pandey P, Saini J, Ramakrishna A, Navalli D, Satishchandra P, Pal PK, Kumar A, Faruq M. Netravathi M, et al. Among authors: faruq m. BMC Med Genet. 2015 Feb 10;16:5. doi: 10.1186/s12881-015-0151-8. BMC Med Genet. 2015. PMID: 25928698 Free PMC article.
167 results