Genetic Factors of Comorbidity of Pelvic Organ Prolapse, Stress Urinary Incontinence, and Chronic Venous Insufficiency of the Lower Limbs in Women

[1]  Liping Tang,et al.  Thermosensitive hydrogels deliver bioactive protein to the vaginal wall , 2017, PloS one.

[2]  Xiaoqi Liu,et al.  A novel FBN1 mutation causes autosomal dominant Marfan syndrome , 2017, Molecular medicine reports.

[3]  J. Raffetto,et al.  Matrix Metalloproteinases in Remodeling of Lower Extremity Veins and Chronic Venous Disease. , 2017, Progress in molecular biology and translational science.

[4]  Ken R. Smith,et al.  Risk for Exfoliation Syndrome in Women With Pelvic Organ Prolapse : A Utah Project on Exfoliation Syndrome (UPEXS) Study. , 2016, JAMA ophthalmology.

[5]  L. Salnikova,et al.  Biological findings from the PheWAS catalog: focus on connective tissue-related disorders (pelvic floor dysfunction, abdominal hernia, varicose veins and hemorrhoids) , 2016, Human Genetics.

[6]  L. Salnikova,et al.  Biological findings from the PheWAS catalog: focus on connective tissue-related disorders (pelvic floor dysfunction, abdominal hernia, varicose veins and hemorrhoids) , 2016, Human Genetics.

[7]  Ping Liu,et al.  LOXL1 Gene Polymorphism With Exfoliation Syndrome/Exfoliation Glaucoma: A Meta-Analysis , 2016, Journal of glaucoma.

[8]  V. Khullar,et al.  Association between joint hypermobility and pelvic organ prolapse in women: a systematic review and meta-analysis , 2016, International Urogynecology Journal.

[9]  Y. Komatsu,et al.  Fibulin-5 deficiency causes developmental defect of premaxillary bone in mice. , 2015, Biochemical and biophysical research communications.

[10]  L. Salnikova,et al.  Elastogenesis-related gene polymorphisms and the risk of pelvic organ prolapse development , 2015, Russian Journal of Genetics.

[11]  V. Puzyrev Genetic bases of human comorbidity , 2015, Russian Journal of Genetics.

[12]  M. Mete,et al.  The Association of Vaginal Wind and Abdominal Striae with Pelvic Organ Prolapse , 2014 .

[13]  P. Handford,et al.  Juvenile idiopathic arthritis, mitral valve prolapse and a familial variant involving the integrin‐binding fragment of FBN1 , 2013, American journal of medical genetics. Part A.

[14]  Victoria L Handa,et al.  Vaginal Childbirth and Pelvic Floor Disorders , 2013, Women's health.

[15]  F. Alizadeh,et al.  The role of pelvic organs prolapse in the etiology of urinary incontinence in women , 2013, Advanced biomedical research.

[16]  Yang Zhou,et al.  Expression and significance of lysyl oxidase-like 1 and fibulin-5 in the cardinal ligament tissue of patients with pelvic floor dysfunction , 2012, Journal of biomedical research.

[17]  Jialiang Zhao,et al.  A novel FBN1 mutation in a Chinese family with isolated ectopia lentis , 2012, Molecular vision.

[18]  K. Kluivers,et al.  Pelvic organ prolapse and collagen-associated disorders , 2011, International Urogynecology Journal.

[19]  D. Sillence,et al.  Mutations in the TGFβ binding-protein-like domain 5 of FBN1 are responsible for acromicric and geleophysic dysplasias. , 2011, American journal of human genetics.

[20]  H. Budka,et al.  Fibulin-5 mutations link inherited neuropathies, age-related macular degeneration and hyperelastic skin. , 2011, Brain : a journal of neurology.

[21]  Madhusudhan Budatha,et al.  Extracellular matrix proteases contribute to progression of pelvic organ prolapse in mice and humans. , 2011, The Journal of clinical investigation.

[22]  G. Walker,et al.  Pelvic organ prolapse and incontinence in developing countries: review of prevalence and risk factors , 2011, International Urogynecology Journal.

[23]  D. Judge,et al.  Mutations in Fibrillin-1 Cause Congenital Scleroderma: Stiff Skin Syndrome , 2010, Science Translational Medicine.

[24]  A. Muñoz,et al.  Vaginal parity and pelvic organ prolapse. , 2010, The Journal of reproductive medicine.

[25]  D. McIntire,et al.  Quantification of Pelvic Organ Prolapse in Mice: Vaginal Protease Activity Precedes Increased MOPQ Scores in Fibulin 5 Knockout Mice1 , 2009, Biology of reproduction.

[26]  G. Pascual,et al.  Down-regulation of lysyl oxydase-like in aging and venous insufficiency. , 2008, Histology and histopathology.

[27]  Kari Stefansson,et al.  Common Sequence Variants in the LOXL1 Gene Confer Susceptibility to Exfoliation Glaucoma , 2007, Science.

[28]  G. Godeau,et al.  Comparison of extracellular matrix in skin and saphenous veins from patients with varicose veins: does the skin reflect venous matrix changes? , 2007, Clinical science.

[29]  O. Nyrén,et al.  Prevalence of symptomatic pelvic organ prolapse in a Swedish population , 2005, International Urogynecology Journal.

[30]  A. Munnich,et al.  In frame fibrillin-1 gene deletion in autosomal dominant Weill-Marchesani syndrome , 2003, Journal of medical genetics.

[31]  A. McTiernan,et al.  Pelvic organ prolapse in the Women's Health Initiative: gravity and gravidity. , 2002, American journal of obstetrics and gynecology.

[32]  Tasuku Honjo,et al.  Fibulin-5/DANCE is essential for elastogenesis in vivo , 2002, Nature.

[33]  G. Cundiff,et al.  Correlation of symptoms with location and severity of pelvic organ prolapse. , 2001, American journal of obstetrics and gynecology.