Associated Papers
Effect of steroid hormone receptor gene variants PROGINS (Alu insertion) and PGR C/T (rs1042839) as a risk factor for recurrent pregnancy loss in Kashmiri population (North India).
Khan N et al.
The Journal of Obstetrics and Gynaecology Research, 2021
The correlation of estrogen receptor 1 and progesterone receptor genes polymorphisms with recurrent pregnancy loss in a cohort of Egyptian women.
Refeat MM et al.
Molecular Biology Reports, 2021
MTHFR (C677T) polymorphism and PR (PROGINS) mutation as genetic factors for preterm delivery, fetal death and low birth weight: A Northeast Indian population based study.
Tiwari D et al.
Meta Gene, 2015
Progesterone receptor variants associated with the PROGINS haplotype exhibit functional properties similar to those of wild-type progesterone receptor.
Stenzig J et al.
Pharmacogenetics and Genomics, 2012
Role of progesterone receptor polymorphisms in the recurrent spontaneous abortions: Indian case.
Aruna M et al.
Plos One, 2010
PROGINS Alu sequence insertion is associated with hyperprolactinaemia but not leiomyoma susceptibility.
Hsieh YY et al.
Clinical Endocrinology, 2005
Association of progesterone receptor polymorphism with recurrent abortions.
Schweikert A et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology, 2004
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