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1.
High incidences of chromosomal aberrations and Y chromosome micro-deletions as prominent causes for recurrent pregnancy losses in highly ethnic and consanguineous population.
Arch Gynecol Obstet
; 305(6): 1393-1408, 2022 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-34542677
2.
Implications of risk conferred by 5p15.33 loci genetic variants; human telomerase reverse transcriptase rs2736098 and rs2736100 in predisposition of bladder cancer.
Rep Pract Oncol Radiother
; 27(5): 787-796, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-36523804
3.
Implications of VEGF gene sequence variations and its expression in recurrent pregnancy loss.
Reprod Biomed Online
; 43(6): 1035-1044, 2021 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-34716101
4.
Influence of prominent immunomodulatory cytokines TNF-α308 G>A (rs1800629) and TGFß1 G>C (rs1800471) sequence variations as an important contributing factor in etiopathogenesis of recurrent miscarriages in Kashmiri women (North India).
J Obstet Gynaecol Res
; 47(5): 1686-1693, 2021 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-33624323
5.
Association of strong risk of hTERT gene polymorphic variants to malignant glioma and its prognostic implications with respect to different histological types and survival of glioma cases.
J Gene Med
; 22(11): e3260, 2020 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-32783258
6.
Possible Impact of RET Polymorphism and Its Haplotypic Association Modulates the Susceptibility to Thyroid Cancer.
J Cell Biochem
; 116(8): 1712-8, 2015 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-25736215
7.
Impact of molecular alterations of BRAF in the pathogenesis of thyroid cancer.
Mutagenesis
; 29(2): 131-7, 2014 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-24442520
8.
Regulatory role of miR-125a expression with respect to its target genes LIFR, ERBB2 and STAT3 in the pathogenesis of recurrent pregnancy losses.
Int J Gynaecol Obstet
; 2024 Mar 25.
Artículo
en Inglés
| MEDLINE | ID: mdl-38528801
9.
Significance and implications of FHIT gene expression and promoter hypermethylation in acute lymphoblastic leukemia (ALL).
Discov Oncol
; 15(1): 108, 2024 Apr 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-38587694
10.
Lack of mutational events of RAS genes in sporadic thyroid cancer but high risk associated with HRAS T81C single nucleotide polymorphism (case-control study).
Tumour Biol
; 34(1): 521-9, 2013 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-23150177
11.
Evaluation of chromosome 1p/19q deletion by Fluorescence in Situ Hybridization (FISH) as prognostic factors in malignant glioma patients on treatment with alkylating chemotherapy.
Cancer Genet
; 278-279: 55-61, 2023 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-37625215
12.
Differential expression of SLITRK6 gene as a potential therapeutic target for urothelial carcinoma in particular upper tract cancer.
Gene
; 878: 147583, 2023 Aug 20.
Artículo
en Inglés
| MEDLINE | ID: mdl-37353040
13.
EPIDERMAL GROWTH FACTOR RECEPTOR (EGFR) POLYMORPHIC VARIATIONS (-216G/T & -191 C/A) POSE A HIGH RISK TO PATIENTS WITH MALIGNANT GLIOMA.
Exp Oncol
; 45(2): 203-210, 2023 10 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-37824771
14.
Burden of cancers in the valley of Kashmir: 5 year epidemiological study reveals a different scenario.
Tumour Biol
; 33(5): 1629-37, 2012 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-22610943
15.
Impact of codon 72 Arg > Pro single nucleotide polymorphism in TP53 gene in the risk of kangri cancer: a case control study in Kashmir.
Tumour Biol
; 33(4): 927-33, 2012 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-22249977
16.
Implications of Decreased Expression of miR-125a with Respect to Its Variant Allele in the Pathogenesis of Recurrent Pregnancy Loss: A Study in a High Incidence Zone.
J Clin Med
; 11(13)2022 Jul 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-35807118
17.
Novelty of Axin 2 and lack of Axin 1 gene mutation in colorectal cancer: a study in Kashmiri population.
Mol Cell Biochem
; 355(1-2): 149-55, 2011 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-21541676
18.
Association of bladder cancer risk with an NAD(P)H:quinone oxidoreductase polymorphism in an ethnic Kashmiri population.
Biochem Genet
; 49(7-8): 417-26, 2011 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-21253823
19.
Impact of ABCB1 Gene (C3435T/A2677G) Polymorphic Sequence Variations on the Outcome of Patients with Chronic Myeloid Leukemia and Acute Lymphoblastic Leukemia in Kashmiri Population: A Case-Control Study.
Indian J Hematol Blood Transfus
; 37(1): 21-29, 2021 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-33707832
20.
Association of APOA1-75G/A and +83C/T polymorphic variation with acute coronary syndrome patients in Kashmir (India).
J Cardiovasc Thorac Res
; 13(2): 109-115, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-34326964