Association of FCRL3 C-169T promoter single-nucleotide polymorphism with idiopathic infertility and infertility-related endometriosis
article
OA: closed
CC0
⤵ 10 in-corpus citations
Limited metadata. Only one source feed has indexed
this record so far — no abstract, full text, or open-access copy is
available through Endo Lab. The
publisher's page (linked below)
is the canonical location for the actual content. If you have institutional
access, use "Find at my library".
AI-generated summary
This study investigated the association between the FCRL3 C-169T promoter single-nucleotide polymorphism and idiopathic infertility and infertility-related endometriosis.
One-sentence paraphrase of the abstract; not a substitute for reading it. No clinical advice. How this works
My notes (saved in your browser only)
Condition tags
MeSH descriptors
Citation neighborhood
Papers in the corpus that this work cites (lower rings, blue) and that cite this one (upper rings, green). Dot size scales with the paper's in-corpus citation count — bigger dot = more influential within the endo/adeno field. Click a dot to open that paper. [ expand to 2 hops ] — adds papers reached through this work's immediate citers/citees. Heavier; up to 60 extra dots.
References (12)
- Involvement of the nuclear factor-κB pathway in the pathogenesis of endometriosis via openalex
- Lymphocytes in Endometriosis via openalex
- Nuclear Factor-κB (NF-κB): An Unsuspected Major Culprit in the Pathogenesis of Endometriosis That Is Still at Large? via openalex
- Revised American Society for Reproductive Medicine classification of endometriosis: 1996 via openalex
- Treating endometriosis as an autoimmune disease via openalex
- W2151809199 via openalex
- W2170025624 via openalex
- W2126718294 via openalex
- W2049704330 via openalex
- W1601356457 via openalex
- W2135029910 via openalex
- W2150491967 via openalex
Cited by (10)
- Genetic basis of endometriosis comorbidity 2024
- Association of FCRL3 Genetic Polymorphisms With Endometriosis-Related Infertility Risk 2015
- Understanding the role of epigenomic, genomic and genetic alterations in the development of endometriosis (Review) 2014
- The FCRL3 −169T>C polymorphism and the risk of endometriosis-related infertility in a Polish population 2013
- Polymorphic variants of DNMT3A and the risk of endometriosis 2012
- Genetic association study of polymorphisms FOXP3 and FCRL3 in women with endometriosis 2012
- Insights into Assessing the Genetics of Endometriosis 2012
- Association of FCRL3 −169T/C polymorphism with endometriosis and identification of a protective haplotype against the development of the disease in Brazilian population 2011
- 10.1016/j.endend.2011.06.063 2000
- 10.1016/j.endend.2011.08.035 2000
Source provenance
- europepmc
- last seen: 2026-06-04T01:30:01.192114+00:00
- openalex
- last seen: 2026-06-04T00:00:01.174412+00:00
- pubmed
- last seen: 2026-05-13T22:16:42.478857+00:00
License: CC0
· commercial use OK