Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Tulin Ibsirlioglu"'
Publikováno v:
Methods. 171:97-107
Here, the in vitro engineering of a cartilage-like tissue by using decellularized extracellular matrix scaffold (hECM) seeded with human adipose stem cells (hASCs) which can both be isolated from the human waste adipose tissue is described. Cell-free
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::680a10f9f69e2643f579c4a42251e66c
https://doi.org/10.1016/j.ymeth.2019.04.020
https://doi.org/10.1016/j.ymeth.2019.04.020
Autor:
Nesrin Besbas, Nicolas G. Bazan, Richard F. Ransom, Chaoying Liang, Edward K. Wakeland, Aysin Bakkaloglu, Tulin Ibsirlioglu, Fatih Ozaltin, Massimo Attanasio, Benjamin E. Wakeland, Komal Vadnagara, Ali Duzova, Emine Korkmaz, Sung Wan An, Richard J. Quigg, Chou Long Huang, Yong Du, Shazia Ashraf, Oguz Soylemezoglu, Alysha Rauhauser, Chandra Mohan, Binghua Li, Deborah Lewis, Friedhelm Hildebrandt, Dongmei Lu, Ekim Z. Taskiran, Rezan Topaloglu, Yelda Bilginer, Phylip Chen, Susan Arbuckle, Seza Ozen, İpek Işık Gönül, Matthew K. Topham
Publikováno v:
Journal of the American Society of Nephrology. 24:377-384
Renal microangiopathies and membranoproliferative GN (MPGN) can manifest similar clinical presentations and histology, suggesting the possibility of a common underlying mechanism in some cases. Here, we performed homozygosity mapping and whole exome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55adf7e24474c48ef2a3733c36e8957e
https://doi.org/10.1681/asn.2012090903
https://doi.org/10.1681/asn.2012090903
Autor:
Serena Bettoni, Ariela Benigni, Paola Cassis, Mira Krendel, Susanna Tomasoni, Giuseppe Remuzzi, Franz Schaefer, Fatih Ozaltin, Fabio Macciardi, Marina Morigi, Marina Noris, Isabella Abbate, Tulin Ibsirlioglu, Carmine Pecoraro, Rossella Piras, Andrea Calabria, Roberta Donadelli, Ramona Maranta, Sevinç Emre, Simona Buelli, Friedhelm Hildebrandt, Paraskevas Iatropoulos, Massimo Delledonne, Caterina Mele, Edgar A. Otto, Maria Rosaria Capobianchi
Publikováno v:
The New England journal of medicine. 365(4)
A B S T R AC T Background Focal segmental glomerulosclerosis is a kidney disease that is manifested as the nephrotic syndrome. It is often resistant to glucocorticoid therapy and progresses to endstage renal disease in 50 to 70% of patients. Genetic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cef20ede7325ded86d337dca13effdc2
https://pubmed.ncbi.nlm.nih.gov/21751899
https://pubmed.ncbi.nlm.nih.gov/21751899
Autor:
Figen Kaymaz, Engin Yilmaz, Beltinge Demircioglu Kilic, Ekim Z. Taskiran, Paraskevas Iatropoulos, Dilek Ertoy Baydar, Nurten A. Akarsu, Aysin Bakkaloglu, Fatih Ozaltin, Mithat Büyükçelik, Ayse Balat, Esin Asan, Franz Schaefer, Tulin Ibsirlioglu
Idiopathic nephrotic syndrome (INS) is a genetically heterogeneous group of disorders characterized by proteinuria, hypoalbuminemia, and edema. Because it typically results in end-stage kidney disease, the steroid-resistant subtype (SRNS) of INS is e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aaa85e8e61d4e5b5de17f85fe6c5268f
http://hdl.handle.net/11655/13922
http://hdl.handle.net/11655/13922
