Detalhe da pesquisa
1.
Missing heritability of Wilson disease: a search for the uncharacterized mutations.
Mamm Genome
; 34(1): 1-11, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36462057
2.
Glutamine deficiency promotes stemness and chemoresistance in tumor cells through DRP1-induced mitochondrial fragmentation.
Cell Mol Life Sci
; 78(10): 4821-4845, 2021 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-33895866
3.
Dopamine ß hydroxylase (DBH) polymorphisms do not contribute towards the clinical course of Wilson's disease in Indian patients.
J Gene Med
; 21(9): e3109, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-31265749
4.
Influence of Apolipoprotein E polymorphism on susceptibility of Wilson disease.
Ann Hum Genet
; 82(2): 53-59, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29059476
5.
Understanding Correlation of Polysomnography Parameters with Drug Induced Sleep Endoscopy in Obstructive Sleep Apnea.
Indian J Otolaryngol Head Neck Surg
; 76(1): 30-35, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38440565
6.
Meta-analysis and prioritization of human skin pigmentation-associated GWAS-SNPs using ENCODE data-based web-tools.
Arch Dermatol Res
; 311(3): 163-171, 2019 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-30756169
7.
Meta-Analysis of Polymorphic Variants Conferring Genetic Risk to Cervical Cancer in Indian Women Supports CYP1A1 as an Important Associated Locus
Asian Pac J Cancer Prev
; 19(8): 2071-2081, 2018 Aug 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-30139066
8.
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.
Neuromolecular Med
; 20(3): 401-408, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-29992511
9.
A clinicopathologic and epidemiologic study of chronic white lesions in the oral mucosa.
Ear Nose Throat J
; 96(8): E13-E17, 2017 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-28846793