Genetic Factors of Comorbidity of Pelvic Organ Prolapse, Stress Urinary Incontinence, and Chronic Venous Insufficiency of the Lower Limbs in Women
暂无分享,去创建一个
[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.