Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Kenan Qin"'
Publikováno v:
Journal of Nutrition and Metabolism, Vol 2011 (2011)
Lipoprotein delivery of fatty acids and cholesterol is linked with peroxisome proliferator-activated receptor (PPAR) activation in adipocytes and macrophages. We postulated that similar interactions exist in sebaceous epithelial cells (sebocytes) in
Externí odkaz:
https://doaj.org/article/2262c5c1c50046f3ac1781ce5b522a32
Publikováno v:
Journal of Networking and Network Applications. 2:172-182
Prediction of learners’ learning styles in online environments has several advantages, including steering learners on the proper path, motivating and engaging them while learning, and improving their learning results. It also helps instructors in t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::973ebaa5ac6f8fd0e444a8056ac1724a
https://doi.org/10.33969/j-nana.2022.020405
https://doi.org/10.33969/j-nana.2022.020405
Publikováno v:
2022 International Conference on Networking and Network Applications (NaNA).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f6ac0eb5044d87b41fbf0c431893eb59
https://doi.org/10.1109/nana56854.2022.00057
https://doi.org/10.1109/nana56854.2022.00057
Publikováno v:
2021 International Conference on Networking and Network Applications (NaNA).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2aa42841b82f415638afed0dab867483
https://doi.org/10.1109/nana53684.2021.00089
https://doi.org/10.1109/nana53684.2021.00089
Publikováno v:
Hormone Research in Paediatrics. 76:434-441
Background/Aims: P450c17 deficiency is an uncommon steroidogenic disorder that typically presents as a sexually infantile adolescent phenotypic female with hypertension and hypokalemia. Although cortisol synthesis is impaired, elevated corticosterone
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e55feb72f65bec4ab6e0288b1a1826b
https://doi.org/10.1159/000329857
https://doi.org/10.1159/000329857
Autor:
Helmuth G. Dörr, Carol Worrell, S. Cabrol, Sojung Lee, Javier de las Heras, Lisa Öhl, Philip Murray, Satz Mengensatzproduktion, Fida Bacha, L. Perin, Brigid Gregg, Christof Schöfl, Thomas M.K. Völkl, M. Jésuran-Perelroizen, Denise L. Jacobson, Christine Yu, Rohan Hazra, Manfred Rauh, Silva A. Arslanian, Olaf Hiort, Tracie L. Miller, Jun Mishina, M. Colle, Y. Le Bouc, Druck Reinhardt Druck Basel, Robert Gut, Robert L. Rosenfield, Peter E. Clayton, Toshiaki Tanaka, Hala Tfayli, William Borkowsky, Linda A. DiMeglio, Larry K. Kociolek, Dan Hanson, Judith L. Ross, Peter A. Lee, Russell B. Van Dyke, R. Coutant, Giampiero I. Baroncelli, Hajime Togari, Eleonora Dati, Kunjal Patel, Susumu Yokoya, John Germak, Silvano Bertelloni, Mitchell E. Geffner, Kenji Fujieda, Yoshiki Seino, Kenan Qin, P. Czernichow, Graeme C.M. Black, Margarita Silio, Anne-Marie Kappelgaard
Publikováno v:
Hormone Research in Paediatrics. 76:I-VI
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e3ce2d17595c59b9c6f9cfd721cdfbf5
https://doi.org/10.1159/000335230
https://doi.org/10.1159/000335230
Autor:
Robert L. Rosenfield, Kenan Qin
Publikováno v:
Steroids. 76:135-139
Hexose-6-phosphate dehydrogenase (H6PD) inactivating mutations cause cortisone reductase deficiency, which manifests with hyperandrogenism unexplained by commonly used tests and, thus, mimics polycystic ovary syndrome (PCOS). The aim of this study wa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98548f8b04b7195dd75532e807a659f3
https://doi.org/10.1016/j.steroids.2010.10.001
https://doi.org/10.1016/j.steroids.2010.10.001
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 94:2594-2601
Kruppel-like factor 15 (KLF15) is a newly discovered transcription factor that plays an important role in glucose homeostasis and lipid accumulation in cells. We present evidence for KLF15 as a transcriptional regulator of the human 17beta-hydroxyste
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9c76b5d62ba794992715712378d82da
https://doi.org/10.1210/jc.2009-0139
https://doi.org/10.1210/jc.2009-0139
Publikováno v:
Pediatric Nephrology. 18:913-918
The unusual coincidence of Bartter syndrome and C1q nephropathy is described and the literature reviewed. An African-American girl presented at 4 years of age with acute hyponatremic dehydration and failure to thrive. Persistent hypokalemic alkalosis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e7c002f90577f7750ce055e9cd46d3d7
https://doi.org/10.1007/s00467-003-1194-1
https://doi.org/10.1007/s00467-003-1194-1
Publikováno v:
Journal of Nutrition and Metabolism, Vol 2011 (2011)
Journal of Nutrition and Metabolism
Journal of Nutrition and Metabolism
Lipoprotein delivery of fatty acids and cholesterol is linked with peroxisome proliferator-activated receptor (PPAR) activation in adipocytes and macrophages. We postulated that similar interactions exist in sebaceous epithelial cells (sebocytes) in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2198b1a341b041c2e5573e4871ab360
https://doaj.org/article/2262c5c1c50046f3ac1781ce5b522a32
https://doaj.org/article/2262c5c1c50046f3ac1781ce5b522a32