Detalhe da pesquisa
1.
The molecular basis for the endocytosis of small R-SNAREs by the clathrin adaptor CALM.
Cell
; 147(5): 1118-31, 2011 Nov 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-22118466
2.
A large-scale conformational change couples membrane recruitment to cargo binding in the AP2 clathrin adaptor complex.
Cell
; 141(7): 1220-9, 2010 Jun 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-20603002
3.
Inhibition of clathrin-mediated endocytosis by knockdown of AP-2 leads to alterations in the plasma membrane proteome.
Traffic
; 22(1-2): 6-22, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33225555
4.
A 24-generation-old founder mutation impairs splicing of RBBP8 in Pakistani families affected with Jawad syndrome.
Clin Genet
; 100(4): 486-488, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34270086
5.
Spastin binds to lipid droplets and affects lipid metabolism.
PLoS Genet
; 11(4): e1005149, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25875445
6.
Sorting Motifs in the Cytoplasmic Tail of the Immunomodulatory E3/49K Protein of Species D Adenoviruses Modulate Cell Surface Expression and Ectodomain Shedding.
J Biol Chem
; 291(13): 6796-812, 2016 Mar 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-26841862
7.
Cutting edge: the UNC93B1 tyrosine-based motif regulates trafficking and TLR responses via separate mechanisms.
J Immunol
; 193(7): 3257-61, 2014 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25187660
8.
Syntaxin binding mechanism and disease-causing mutations in Munc18-2.
Proc Natl Acad Sci U S A
; 110(47): E4482-91, 2013 Nov 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-24194549
9.
FCHO controls AP2's initiating role in endocytosis through a PtdIns(4,5)P2-dependent switch.
Sci Adv
; 8(17): eabn2018, 2022 Apr 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-35486718
10.
De novo variants of CSNK2B cause a new intellectual disability-craniodigital syndrome by disrupting the canonical Wnt signaling pathway.
HGG Adv
; 3(3): 100111, 2022 Jul 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-35571680
11.
AP-4 binds basolateral signals and participates in basolateral sorting in epithelial MDCK cells.
Nat Cell Biol
; 4(2): 154-9, 2002 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-11802162
12.
Hypoxia-inducible protein 2 is a novel lipid droplet protein and a specific target gene of hypoxia-inducible factor-1.
FASEB J
; 24(11): 4443-58, 2010 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-20624928
13.
Modifier Genes in Microcephaly: A Report on WDR62, CEP63, RAD50 and PCNT Variants Exacerbating Disease Caused by Biallelic Mutations of ASPM and CENPJ.
Genes (Basel)
; 12(5)2021 05 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-34068194
14.
AP-1 and AP-3 mediate sorting of melanosomal and lysosomal membrane proteins into distinct post-Golgi trafficking pathways.
Traffic
; 9(7): 1157-72, 2008 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-18410487
15.
The clavesin family, neuron-specific lipid- and clathrin-binding Sec14 proteins regulating lysosomal morphology.
J Biol Chem
; 284(40): 27646-54, 2009 Oct 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-19651769
16.
The adaptor protein AP-3 is required for CD1d-mediated antigen presentation of glycosphingolipids and development of Valpha14i NKT cells.
J Exp Med
; 198(8): 1133-46, 2003 Oct 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-14557411
17.
Microtubule-dependent and independent roles of spastin in lipid droplet dispersion and biogenesis.
Life Sci Alliance
; 3(6)2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32321733
18.
Cytosolic Gram-negative bacteria prevent apoptosis by inhibition of effector caspases through lipopolysaccharide.
Nat Microbiol
; 5(2): 354-367, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31873204
19.
An update of pathogenic variants in ASPM, WDR62, CDK5RAP2, STIL, CENPJ, and CEP135 underlying autosomal recessive primary microcephaly in 32 consanguineous families from Pakistan.
Mol Genet Genomic Med
; 8(9): e1408, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32677750
20.
A mutation in the signal sequence of LRP5 in a family with an osteoporosis-pseudoglioma syndrome (OPPG)-like phenotype indicates a novel disease mechanism for trinucleotide repeats.
Hum Mutat
; 30(4): 641-8, 2009 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-19177549