Detalhe da pesquisa
1.
Mfsd7b facilitates choline transport and missense mutations affect choline transport function.
Cell Mol Life Sci
; 81(1): 3, 2023 Dec 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-38055060
2.
Postnatal deletion of Spns2 prevents neuroinflammation without compromising blood vascular functions.
Cell Mol Life Sci
; 79(11): 541, 2022 Oct 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36198832
3.
Erythrocytes efficiently utilize exogenous sphingosines for S1P synthesis and export via Mfsd2b.
J Biol Chem
; 296: 100201, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33334894
4.
Convenient synthesis of deazaflavin cofactor FO and its activity in F(420)-dependent NADP reductase.
Org Biomol Chem
; 13(18): 5082-5, 2015 May 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-25827330
5.
Lack of SPNS1 results in accumulation of lysolipids and lysosomal storage disease in mouse models.
JCI Insight
; 9(8)2024 Mar 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-38451736
6.
MFSD7c functions as a transporter of choline at the blood-brain barrier.
Cell Res
; 34(3): 245-257, 2024 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-38302740
7.
Mfsd2b and Spns2 are essential for maintenance of blood vessels during development and in anaphylactic shock.
Cell Rep
; 40(7): 111208, 2022 08 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-35977478
8.
Deficiency of MFSD7c results in microcephaly-associated vasculopathy in Fowler syndrome.
J Clin Invest
; 130(8): 4081-4093, 2020 08 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-32369449