Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Soumia Brakta"'
Publikováno v:
Stem Cell Research & Therapy, Vol 9, Iss 1, Pp 1-8 (2018)
Abstract Background Myometrium, the muscular wall of the uterus, is an active organ markedly remodeled during a woman’s reproductive life, especially during pregnancy. Different studies using the 5-bromo-2′-deoxyuridine and side population method
Externí odkaz:
https://doaj.org/article/fc8887d4dd1d4be8b105e7a0c1c5a923
Publikováno v:
SAGE Open Medical Case Reports, Vol 8 (2020)
Fibrothecomas are mostly benign ovarian tumors. We describe a rare case of fibrothecoma in a 59-year-old woman with a history of recurrent massive ascites and postmenopausal bleeding. Over 2 years she has undergone more than 50 paracenteses with 8–
Externí odkaz:
https://doaj.org/article/48f2f198a1744b4fa4f0cdc22dca3798
Autor:
Jonathan D. J. Labonne, Terri M. Driessen, Marvin E. Harris, Il-Keun Kong, Soumia Brakta, John Theisen, Modibo Sangare, Lawrence C. Layman, Cheol-Hee Kim, Janghoo Lim, Hyung-Goo Kim
Publikováno v:
Journal of Clinical Medicine, Vol 9, Iss 1, p 274 (2020)
We report a genomic and phenotypic delineation for two chromosome regions with candidate genes for syndromic intellectual disability at 12q12 and Xp22.31, segregating independently in one family with four affected members. Fine mapping of three affec
Externí odkaz:
https://doaj.org/article/f160c4a569c2441f8d54dc00c2ef0ffa
Autor:
Sara A. Mohamed, Shahinaz Shalaby, Soumia Brakta, Lelyand Elam, Amro Elsharoud, Ayman Al-Hendy
Publikováno v:
Biomedicines, Vol 7, Iss 1, p 7 (2019)
Background: Premature ovarian insufficiency (POI) is a challenging disease, with limited treatment options at the moment. Umbilical cord blood mesenchymal stem cells (UCMSCs) have demonstrated promising regenerative abilities in several diseases incl
Externí odkaz:
https://doaj.org/article/c4fe4e66c0294219986a165ae65fd3d4
Autor:
Soumia Brakta, Zoe A. Hawkins, Nikhil Sahajpal, Natalie Seman, Dina Kira, Lynn P. Chorich, Hyung-Goo Kim, Hongyan Xu, John A. Phillips, Ravindra Kolhe, Lawrence C. Layman
Publikováno v:
Human Genetics. 142:483-494
Autor:
Michael P. Dougherty, Alexandra M. Poch, Lynn P. Chorich, Zoe A. Hawkins, Hongyan Xu, Robert A. Roman, Haitao Liu, Soumia Brakta, Hugh S. Taylor, James Knight, Hyung-Goo Kim, Michael P. Diamond, Lawrence C. Layman
Publikováno v:
New England Journal of Medicine. 388:1055-1056
Publikováno v:
Fertility and Sterility. 111:389-396
Objective To test the hypothesis that the polycystic ovary syndrome (PCOS) phenotype, or its component features, is less severe in adolescents than in young adult patients, in a referred (clinical) population. Design Cross-sectional study. Setting Te
Publikováno v:
SAGE Open Medical Case Reports
SAGE Open Medical Case Reports, Vol 8 (2020)
SAGE Open Medical Case Reports, Vol 8 (2020)
Fibrothecomas are mostly benign ovarian tumors. We describe a rare case of fibrothecoma in a 59-year-old woman with a history of recurrent massive ascites and postmenopausal bleeding. Over 2 years she has undergone more than 50 paracenteses with 8–
Autor:
Laurel A. Coons, Hyung-Goo Kim, John A. Katzenellenbogen, Kenneth S. Korach, Lynn P. Chorich, Janet E. Hall, Lawrence C. Layman, Soumia Brakta
Publikováno v:
J Clin Endocrinol Metab
ContextWe previously reported the first female with a causative ESR1 gene variant, who exhibited absent puberty and high estrogens. At age 15 years, she presented with lower abdominal pain, absent breast development, primary amenorrhea, and multicyst
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d5205bf2010c2a54643c64a28a805b3
https://europepmc.org/articles/PMC7108680/
https://europepmc.org/articles/PMC7108680/
Autor:
Kim, Jonathan D. J. Labonne, Terri M. Driessen, Marvin E. Harris, Il-Keun Kong, Soumia Brakta, John Theisen, Modibo Sangare, Lawrence C. Layman, Cheol-Hee Kim, Janghoo Lim, Hyung-Goo
Publikováno v:
Journal of Clinical Medicine; Volume 9; Issue 1; Pages: 274
We report a genomic and phenotypic delineation for two chromosome regions with candidate genes for syndromic intellectual disability at 12q12 and Xp22.31, segregating independently in one family with four affected members. Fine mapping of three affec