A proteína do núcleo de sialomucina 24 também conhecida como CD164 (Grupo de diferenciação 164) é uma proteína que em humanos é codificada pelo gene CD164.[3][4] O CD164 funciona como uma molécula de adesão celular.[3]
Referências
- ↑ «Doenças geneticamente associadas a CD164 ver/editar referências no wikidata»
- ↑ «Human PubMed Reference:»
- ↑ a b Watt SM, Bühring HJ, Rappold I, Chan JY, Lee-Prudhoe J, Jones T, Zannettino AC, Simmons PJ, Doyonnas R, Sheer D, Butler LH (Agosto de 1998). «CD164, a novel sialomucin on CD34(+) and erythroid subsets, is located on human chromosome 6q21». Blood. 92 (3): 849–66. PMID 9680353
- ↑ Zannettino AC, Bühring HJ, Niutta S, Watt SM, Benton MA, Simmons PJ (Outubro de 1998). «The sialomucin CD164 (MGC-24v) is an adhesive glycoprotein expressed by human hematopoietic progenitors and bone marrow stromal cells that serves as a potent negative regulator of hematopoiesis». Blood. 92 (8): 2613–28. PMID 9763543
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Doyonnas R, Yi-Hsin Chan J, Butler LH, et al. (2000). «CD164 monoclonal antibodies that block hemopoietic progenitor cell adhesion and proliferation interact with the first mucin domain of the CD164 receptor». J. Immunol. 165 (2): 840–51. PMID 10878358. doi:10.4049/jimmunol.165.2.840 *
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Havens AM, Jung Y, Sun YX, et al. (2006). «The role of sialomucin CD164 (MGC-24v or endolyn) in prostate cancer metastasis». BMC Cancer. 6. 195 páginas. PMC 1557671. PMID 16859559. doi:10.1186/1471-2407-6-195 *
Forde S, Tye BJ, Newey SE, et al. (2007). «Endolyn (CD164) modulates the CXCL12-mediated migration of umbilical cord blood CD133+ cells». Blood. 109 (5): 1825–33. PMID 17077324. doi:10.1182/blood-2006-05-023028 *
Strausberg RL, Feingold EA, Grouse LH, et al. (2002). «Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences». Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. PMC 139241. PMID 12477932. doi:10.1073/pnas.242603899 *
Hennersdorf F, Florian S, Jakob A, et al. (2005). «Identification of CD13, CD107a, and CD164 as novel basophil-activation markers and dissection of two response patterns in time kinetics of IgE-dependent upregulation». Cell Res. 15 (5): 325–35. PMID 15916720. doi:10.1038/sj.cr.7290301