Zobrazeno 1 - 4
of 4
pro vyhledávání: '"David Eric Anderson"'
Autor:
Annika Pfeiffer, Jennifer D. Petersen, Guido H. Falduto, David Eric Anderson, Joshua Zimmerberg, Dean D. Metcalfe, Ana Olivera
Publikováno v:
Journal of Extracellular Vesicles, Vol 11, Iss 10, Pp n/a-n/a (2022)
Abstract Activating mutations in the receptor KIT promote the dysregulated proliferation of human mast cells (huMCs). The resulting neoplastic huMCs secrete extracellular vesicles (EVs) that can transfer oncogenic KIT among other cargo into recipient
Externí odkaz:
https://doaj.org/article/165c68a2761947fb95bb85c81dfb9874
Publikováno v:
International Journal of Molecular Sciences, Vol 21, Iss 3, p 895 (2020)
Human tyrosinase (Tyr) is involved in pigment biosynthesis, where mutations in its corresponding gene TYR have been linked to oculocutaneous albinism 1, an autosomal recessive disorder. Although the enzymatic capabilities of Tyr have been well-charac
Externí odkaz:
https://doaj.org/article/fbfd84ff9d83447e8ab7412ae219d875
Publikováno v:
International Journal of Molecular Sciences
Volume 21
Issue 3
International Journal of Molecular Sciences, Vol 21, Iss 3, p 895 (2020)
Volume 21
Issue 3
International Journal of Molecular Sciences, Vol 21, Iss 3, p 895 (2020)
Human tyrosinase (Tyr) is involved in pigment biosynthesis, where mutations in its corresponding gene TYR have been linked to oculocutaneous albinism 1, an autosomal recessive disorder. Although the enzymatic capabilities of Tyr have been well-charac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d00707e02e9bf9710723ec7a3a592ce
https://hdl.handle.net/10919/97090
https://hdl.handle.net/10919/97090
Autor:
Jun Hayakawa, John F. Tisdale, Naoya Uchida, Kareem Washington, Matthew M. Hsieh, Oswald Phang, David Eric Anderson
Publikováno v:
Blood. 112:2446-2446
Xenografting immunodeficient mice has been employed as a surrogate human hematopoietic stem cell (HSC) assay, however, erythroid output has not been reliably reported, limiting the usefulness of this model for erythroid disorders. We have previously