Detalles de la búsqueda
1.
Association between opioid and dopamine receptor gene polymorphisms OPRM1 rs1799971, DAT VNTR 9-10 repeat allele, DRD1 rs4532 and DRD2 rs1799732 and alcohol dependence: an ethnicity oriented meta-analysis.
Pharmacogenet Genomics
; 33(7): 139-152, 2023 09 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-37466123
2.
Impact of Serotonin Pathway Gene Polymorphisms and Serotonin Levels in Suicidal Behavior.
Med Princ Pract
; 2023 Sep 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-37717578
3.
Differential urinary microRNA expression analysis of miR-1, miR-215, miR-335, let-7a in childhood nephrotic syndrome.
Mol Biol Rep
; 49(7): 6591-6600, 2022 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-35553329
4.
Role of serotonin transporter and receptor gene polymorphisms in treatment response to selective serotonin reuptake inhibitors in major depressive disorder.
Hum Psychopharmacol
; 37(4): e2830, 2022 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-34994008
5.
MicroRNAs in childhood nephrotic syndrome.
J Cell Physiol
; 236(10): 7186-7210, 2021 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-33819345
6.
Association of Serum Biomarker Levels and BDNF Gene Polymorphism with Response to Selective Serotonin Reuptake Inhibitors in Indian Patients with Major Depressive Disorder.
Neuropsychobiology
; 80(3): 201-213, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-32731218
7.
Differentially expressed miR-20, miR-21, miR-100, miR-125a and miR-146a as a potential biomarker for prostate cancer.
Mol Biol Rep
; 48(4): 3349-3356, 2021 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-33948855
8.
Differential expression of microRNAs let-7a, miR-125b, miR-100, and miR-21 and interaction with NF-kB pathway genes in periodontitis pathogenesis.
J Cell Physiol
; 233(8): 5877-5884, 2018 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-29226952
9.
Report of novel genetic variation in NPHS2 gene associated with idiopathic nephrotic syndrome in South Indian children.
Clin Exp Nephrol
; 21(1): 127-133, 2017 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-26820844
10.
Genetic variation in matrix metalloproteinase MMP2 and MMP9 as a risk factor for idiopathic recurrent spontaneous abortions in an Indian population.
J Assist Reprod Genet
; 34(7): 945-949, 2017 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-28500450
11.
The A1298C Methylenetetrahydrofolate Reductase Gene Variant as a Susceptibility Gene for Non-Syndromic Conotruncal Heart Defects in an Indian Population.
Pediatr Cardiol
; 36(7): 1470-5, 2015 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-25981563
12.
Single nucleotide polymorphisms of enamel formation genes and early childhood caries - systematic review, gene-based, gene cluster and meta-analysis.
J Indian Soc Pedod Prev Dent
; 41(1): 3-15, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-37282406
13.
Erratum to: Report of novel genetic variation in NPHS2 gene associated with idiopathic nephrotic syndrome in South Indian children.
Clin Exp Nephrol
; 21(1): 134-135, 2017 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-27465543
14.
Burden of Type 2 Diabetes and Associated Cardiometabolic Traits and Their Heritability Estimates in Endogamous Ethnic Groups of India: Findings From the INDIGENIUS Consortium.
Front Endocrinol (Lausanne)
; 13: 847692, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-35498404
15.
Clonal hematopoiesis of indeterminate potential (CHIP) and cardiovascular diseases-an updated systematic review.
J Genet Eng Biotechnol
; 19(1): 105, 2021 Jul 19.
Artículo
en Inglés
| MEDLINE | ID: mdl-34279740
16.
Genetic Polymorphisms in miR-146a, miR-196a2 and miR-125a Genes and its Association in Prostate Cancer.
Pathol Oncol Res
; 26(1): 193-200, 2020 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-29594807
17.
A case-control association of RANTES (-28Câ¯>G) and CCR5-Delta32 polymorphisms with Parkinson's disease in Indians.
Neurosci Lett
; 739: 135404, 2020 11 20.
Artículo
en Inglés
| MEDLINE | ID: mdl-32987132
18.
Clinical, biochemical and genetic characteristics of children with congenital adrenal hyperplasia due to 17α-hydroxylase deficiency.
J Pediatr Endocrinol Metab
; 2020 Jul 13.
Artículo
en Inglés
| MEDLINE | ID: mdl-32651986
19.
Study on the SFRP4 gene polymorphism and expression in prostate cancer.
J Genet
; 992020.
Artículo
en Inglés
| MEDLINE | ID: mdl-33361638
20.
Mutation Analysis Using Multiplex Ligation-Dependent Probe Amplification in Consanguineous Families in South India with a Child with Profound Hearing Impairment.
Lab Med
; 51(1): 56-65, 2020 Jan 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-31150550