Human Genome Epidemiology Literature Finder
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Records 1 - 5 (of 5 Records) |
| Query Trace: Pelvic Organ Prolapse and LOXL1[original query] |
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| A single nucleotide polymorphism in the promoter of the LOXL1 gene and its relationship to pelvic organ prolapse and preterm premature rupture of membranes. Reproductive sciences (Thousand Oaks, Calif.) 2009 May 16 (5): 438-46. Ferrell Georgia, Lu Minyan, Stoddard Paul, Sammel Mary D, Romero Roberto, Strauss Jerome F, Matthews Catherine |
| Mutation screen of LOXL1 in patients with female pelvic organ prolapse. Female pelvic medicine & reconstructive surgery 0 20 (6): 316-21. Neupane Ruel, Sadeghi Zhina, Fu Rao, Hagstrom Stephanie A, Moore Courtenay K, Daneshgari Firo |
| [Elastogenesis-Related Gene Polymorphisms and the Risk of Pelvic Organ Prolapse Development]. Genetika 2015 Oct 51 (10): 1191-8. Khadzhieva M B, Kamoeva S V, Ivanova A V, Abilev S K, Salnikova L |
| Collagen type 1A1, type 3A1, and LOXL1/4 polymorphisms as risk factors of pelvic organ prolapse. BMC research notes 2021 Jan 14 (1): 15. Ashikari Asuka, Suda Tetsuji, Miyazato Mino |
| The rs2165241 polymorphism of the Loxl1 gene in postmenopausal women with pelvic organ prolapse. Climacteric : the journal of the International Menopause Society 2022 4 25 (4): 407-412. Costa E Silva C L, Bortolini M A T, Batista N C, Silva R S P, Teixeira J B, Oliveira É, Souto R P, Castro R |
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