Ina Amin
Srinagar, JK 190011, India
Last Updated: 09/26/2026
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Found 10 publications
Polymorphic Variants of FOXP3 Gene (rs 3761548) and (rs 3761549) are Significantly Associated with the Risk for Recurrent Pregnancy Losses. A Study in High Incidence Zone (Kashmir, North India).
Journal: Journal of mother and child
Published: August 11, 2025
Significant Implications Of miR-126 Expression With Respect to Its Target Gene VEGFA in the Pathogenesis of Recurrent Pregnancy Losses (RPL)-a Study in High Incidence Zone.
Journal: Reproductive sciences (Thousand Oaks, Calif.)
Published: May 14, 2025
Regulatory role of miR-125a expression with respect to its target genes LIFR, ERBB2 and STAT3 in the pathogenesis of recurrent pregnancy losses.
Journal: International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics
Published: April 25, 2023
Implications of risk conferred by 5p15.33 loci genetic variants; human telomerase reverse transcriptase rs2736098 and rs2736100 in predisposition of bladder cancer.
Journal: Reports of practical oncology and radiotherapy : journal of Greatpoland Cancer Center in Poznan and Polish Society of Radiation Oncology
Published: May 14, 2022
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.
Journal: Journal of clinical medicine
Published: April 26, 2022
Implications of VEGF gene sequence variations and its expression in recurrent pregnancy loss.
Journal: Reproductive biomedicine online
Published: June 04, 2021
Analysis of MNS16A VNTR polymorphic sequence variations of the TERT gene and associated risk for development of bladder cancer.
Journal: Current urology
Published: September 27, 2020
Influence of prominent immunomodulatory cytokines TNF-α308 G>A (rs1800629) and TGFβ1 G>C (rs1800471) sequence variations as an important contributing factor in etiopathogenesis of recurrent miscarriages in Kashmiri women (North India).
Journal: The journal of obstetrics and gynaecology research
Published: July 18, 2020
High incidences of chromosomal aberrations and Y chromosome micro-deletions as prominent causes for recurrent pregnancy losses in highly ethnic and consanguineous population.
Journal: Archives of gynecology and obstetrics
Published: February 05, 2020
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.
Journal: The journal of gene medicine
Published: February 05, 2020
Showing 1-10 of 10
Last Updated: 09/26/2026