Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Hailu Shitaye"'
Autor:
Ellen A. Tsai, Melissa A. Gilbert, Christopher M. Grochowski, Lara A. Underkoffler, He Meng, Xiaojie Zhang, Michael M. Wang, Hailu Shitaye, Kurt D. Hankenson, David Piccoli, Henry Lin, Binita M. Kamath, Marcella Devoto, Nancy B. Spinner, Kathleen M. Loomes
Publikováno v:
Cellular and Molecular Gastroenterology and Hepatology, Vol 2, Iss 5, Pp 663-675.e2 (2016)
Background & Aims: Alagille syndrome is an autosomal-dominant, multisystem disorder caused primarily by mutations in JAG1, resulting in bile duct paucity, cholestasis, cardiac disease, and other features. Liver disease severity in Alagille syndrome i
Externí odkaz:
https://doaj.org/article/b1059066274f46d2a191417369a2f263
Publikováno v:
Current Osteoporosis Reports. 8:68-76
Thrombospondins (TSPs) are a family of five secreted multimeric matricellular proteins that share homology in the type II and III repeats and carboxy-terminal region. Type I repeats, also known as properdin or thrombospondin repeats (TSRs), are found
Autor:
Christina N. Bennett, Michael Friedman, Weijun Luo, Ormond A. MacDougald, Kurt D. Hankenson, Joshua W. Miller, Hailu Shitaye
Publikováno v:
Experimental Cell Research. 314:3382-3391
Differentiation of marrow-derived mesenchymal progenitors to either the osteoblast or adipocyte lineage is reciprocally regulated. Factors that promote osteoblastogenesis inhibit adipogenesis, while adipogenic factors are inhibitory to osteoblast dif
The matricellular protein thrombospondin-2 (TSP2) inhibits proliferation and enhances osteoblastogenesis of multipotent mesenchymal progenitor cells (MPC). Osteoblastogenesis and adipogenesis are reciprocally regulated, thus we hypothesized that TSP2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39de1272a870f16ab75499e8fc93b535
https://europepmc.org/articles/PMC2939302/
https://europepmc.org/articles/PMC2939302/
Publikováno v:
Human immunology. 60(12)
The function of the TAP gene products appears to be the transport of antigenic peptides into the lumen of the endoplasmic reticulum where peptides are loaded onto HLA molecules. The polymorphisms within the TAP genes and potential disease association
Publikováno v:
Bone. 42:S23
Publikováno v:
Matrix Biology. 25:S23-S23
Autor:
Kurt D. Hankenson, David A. Piccoli, Ellen A. Tsai, Lara A. Underkoffler, Michael M. Wang, Binita M. Kamath, He Meng, Christopher M. Grochowski, Hailu Shitaye, Marcella Devoto, Nancy B. Spinner, Henry C. Lin, Melissa A. Gilbert, Xiaojie Zhang, Kathleen M. Loomes
Publikováno v:
Cellular and Molecular Gastroenterology and Hepatology, Vol 2, Iss 5, Pp 663-675.e2 (2016)
Cellular and Molecular Gastroenterology and Hepatology
Cellular and Molecular Gastroenterology and Hepatology
Background & Aims: Alagille syndrome is an autosomal-dominant, multisystem disorder caused primarily by mutations in JAG1, resulting in bile duct paucity, cholestasis, cardiac disease, and other features. Liver disease severity in Alagille syndrome i