Výsledky vyhledávání - "I. P. Meschede"

Myosin Va interacts with the exosomal protein spermine synthase

Autor: A.F.Z. Nascimento, Rui M.P. da Silva-Júnior, Leandro H.P. Assis, Jackeline S. Araujo, Mário T. Murakami, Priscila Oliveira de Giuseppe, Enilza Maria Espreáfico, Luciano G. Dolce, I. P. Meschede

Publikováno v: Bioscience Reports
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP

A recent paper in Bioscience Reports (BSR20182189) describes the discovery of an interaction between the motor protein myosin Va and the metabolic enzyme spermine synthase. Myosin Va is a molecular motor which plays a key role in vesicle transport. M

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::06133eb760a2223dc70d105d6905e0be
https://pubmed.ncbi.nlm.nih.gov/30967493

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Griscelli syndrome-type 2 in twin siblings: case report and update on RAB27A human mutations and gene structure

Autor: T C Izidoro-Toledo, J Gurgel-Gianetti, T O Santos, Enilza Maria Espreáfico, I. P. Meschede

Publikováno v: Brazilian Journal of Medical and Biological Research v.41 n.10 2008
Brazilian Journal of Medical and Biological Research
Associação Brasileira de Divulgação Científica (ABDC)
instacron:ABDC
Brazilian Journal of Medical and Biological Research, Vol 41, Iss 10, Pp 839-848 (2008)
Brazilian Journal of Medical and Biological Research, Volume: 41, Issue: 10, Pages: 839-848, Published: OCT 2008

Griscelli syndrome (GS) is a rare autosomal recessive disorder caused by mutation in the MYO5A (GS1, Elejalde), RAB27A (GS2) or MLPH (GS3) genes. Typical features of all three subtypes of this disease include pigmentary dilution of the hair and skin

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d4fb3f6e3bdede832ee49b7401ca371
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2008001000002

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