Pages that link to "Q53450118"
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The following pages link to Genetic factors contribute to the risk of developing endometriosis. (Q53450118):
Displaying 50 items.
- Genomewide linkage study in 1,176 affected sister pair families identifies a significant susceptibility locus for endometriosis on chromosome 10q26. (Q24533776) (← links)
- Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis (Q24601618) (← links)
- Genetics of endometriosis (Q26781710) (← links)
- Defining future directions for endometriosis research: workshop report from the 2011 World Congress of Endometriosis In Montpellier, France (Q26823337) (← links)
- Environmental factors and endometriosis (Q27020952) (← links)
- Genome-wide association study link novel loci to endometriosis (Q28286869) (← links)
- Dysregulated sphingolipid metabolism in endometriosis (Q33570165) (← links)
- Adenomyosis and endometriosis in the California Teachers Study (Q33619769) (← links)
- Research resource: genome-wide profiling of methylated promoters in endometriosis reveals a subtelomeric location of hypermethylation (Q33637255) (← links)
- The dynamics of nuclear receptors and nuclear receptor coregulators in the pathogenesis of endometriosis (Q33778690) (← links)
- Common Variation in the CYP17A1 and IFIT1 Genes on Chromosome 10 Does Not Contribute to the Risk of Endometriosis (Q33799502) (← links)
- Common variation in the fibroblast growth factor receptor 2 gene is not associated with endometriosis risk (Q33988532) (← links)
- Endometriosis is associated with rare copy number variants (Q33989579) (← links)
- Shift work, hCLOCK T3111C polymorphism, and endometriosis risk (Q34097100) (← links)
- Null genotypes of GSTM1 and GSTT1 and endometriosis risk: a meta-analysis of 25 case-control studies (Q34160170) (← links)
- No association of GSTM1 null polymorphism with endometriosis in women from central and southern Iran (Q34176393) (← links)
- MUC2 polymorphisms are associated with endometriosis development and infertility: a case-control study (Q34195190) (← links)
- Risk Factors for Endometriosis in a German Case-Control Study (Q34201814) (← links)
- Bladder endometriosis, a remarkable resemblance in a monozygotic twin (Q34283970) (← links)
- Severe teenage acne and risk of endometriosis (Q34313208) (← links)
- Advances in the genetics of endometriosis (Q34334093) (← links)
- Complex genotype sarcomas display familial inheritance independent of known cancer predisposition syndromes (Q34892763) (← links)
- Emerging role of genomics in endometriosis research (Q34953119) (← links)
- Endometriosis and Chronic Pelvic Pain: Unraveling the Mystery Behind this Complex Condition (Q34987786) (← links)
- Stem cells and the pathogenesis of endometriosis (Q35023781) (← links)
- BMPR1B up-regulation via a miRNA binding site variation defines endometriosis susceptibility and CA125 levels (Q35067319) (← links)
- High-density fine-mapping of a chromosome 10q26 linkage peak suggests association between endometriosis and variants close to CYP2C19 (Q35074952) (← links)
- Genetics of endometriosis. (Q35108915) (← links)
- Record review of baboons with histologically confirmed endometriosis in a large established colony (Q35122415) (← links)
- Incidence of endometriosis by study population and diagnostic method: the ENDO study (Q35126918) (← links)
- Genetics and genomics of endometriosis (Q35136686) (← links)
- Whole-exome sequencing of endometriosis identifies frequent alterations in genes involved in cell adhesion and chromatin-remodeling complexes (Q35195877) (← links)
- Coding regions of INHBA, SFRP4 and HOXA10 are not implicated in familial endometriosis linked to chromosome 7p13–15 (Q35210453) (← links)
- Heritability and candidate genes for endometriosis (Q35563794) (← links)
- Genetic variation in the sex hormone metabolic pathway and endometriosis risk: an evaluation of candidate genes (Q35587188) (← links)
- Insights into Assessing the Genetics of Endometriosis (Q36133689) (← links)
- Cellular and molecular basis for endometriosis-associated infertility. (Q36195426) (← links)
- No evidence for genetic association with the let-7 microRNA-binding site or other common KRAS variants in risk of endometriosis (Q36408602) (← links)
- Estrogen receptor β regulates endometriotic cell survival through serum and glucocorticoid-regulated kinase activation (Q36858524) (← links)
- Priorities for endometriosis research: recommendations from an international consensus workshop. (Q36929234) (← links)
- The search for genes contributing to endometriosis risk (Q36953384) (← links)
- Common variants upstream of KDR encoding VEGFR2 and in TTC39B associate with endometriosis (Q37129450) (← links)
- Developmental exposure of fetal ovaries and fetal germ cells to endometriosis in an endometriosis model causes differential gene expression in the preimplantation embryos of the first-generation and second-generation embryos. (Q37358218) (← links)
- A novel endometriosis inducing factor in women with endometriosis (Q37536146) (← links)
- Prostaglandin E2: the master of endometriosis? (Q37761617) (← links)
- Endometrial adult/progenitor stem cells: pathogenetic theory and new antiangiogenic approach for endometriosis therapy. (Q38137804) (← links)
- Endometriosis: pathogenesis and treatment. (Q38173642) (← links)
- The role of gene polymorphisms in endometriosis. (Q40044064) (← links)
- Replication of endometriosis-associated single-nucleotide polymorphisms from genome-wide association studies in a Caucasian population (Q43920132) (← links)
- Association between polymorphisms in the progesterone receptor gene and endometriosis (Q46673590) (← links)