Detalhe da pesquisa
1.
Opitz syndrome: improving clinical interpretation of intronic variants in MID1 gene.
Pediatr Res
; 93(5): 1208-1215, 2023 04.
Artigo
Inglês
| MEDLINE | ID: mdl-35953512
2.
TRIM E3 Ubiquitin Ligases in Rare Genetic Disorders.
Adv Exp Med Biol
; 1233: 311-325, 2020.
Artigo
Inglês
| MEDLINE | ID: mdl-32274764
3.
The E3 ubiquitin ligase MID1/TRIM18 promotes atypical ubiquitination of the BRCA2-associated factor 35, BRAF35.
Biochim Biophys Acta Mol Cell Res
; 1864(10): 1844-1854, 2017 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-28760657
4.
The combination of transcriptomics and informatics identifies pathways targeted by miR-204 during neurogenesis and axon guidance.
Nucleic Acids Res
; 42(12): 7793-806, 2014 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-24895435
5.
Midline 1 directs lytic granule exocytosis and cytotoxicity of mouse killer T cells.
Eur J Immunol
; 44(10): 3109-18, 2014 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-25043946
6.
TRIM family: Pleiotropy and diversification through homomultimer and heteromultimer formation.
IUBMB Life
; 64(1): 64-71, 2012 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-22131136
7.
Functional interactions between ubiquitin E2 enzymes and TRIM proteins.
Biochem J
; 434(2): 309-19, 2011 Mar 01.
Artigo
Inglês
| MEDLINE | ID: mdl-21143188
8.
Genomics and evolution of the TRIM gene family.
Adv Exp Med Biol
; 770: 1-9, 2012.
Artigo
Inglês
| MEDLINE | ID: mdl-23630996
9.
TRIM proteins in development.
Adv Exp Med Biol
; 770: 131-41, 2012.
Artigo
Inglês
| MEDLINE | ID: mdl-23631005
10.
Cellular Function of TRIM E3 Ubiquitin Ligases in Health and Disease.
Cells
; 11(2)2022 01 12.
Artigo
Inglês
| MEDLINE | ID: mdl-35053366
11.
Microtubular TRIM36 E3 Ubiquitin Ligase in Embryonic Development and Spermatogenesis.
Cells
; 11(2)2022 01 12.
Artigo
Inglês
| MEDLINE | ID: mdl-35053362
12.
SPECC1L Mutations Are Not Common in Sporadic Cases of Opitz G/BBB Syndrome.
Genes (Basel)
; 13(2)2022 01 28.
Artigo
Inglês
| MEDLINE | ID: mdl-35205294
13.
Lack of Mid1, the mouse ortholog of the Opitz syndrome gene, causes abnormal development of the anterior cerebellar vermis.
J Neurosci
; 30(8): 2880-7, 2010 Feb 24.
Artigo
Inglês
| MEDLINE | ID: mdl-20181585
14.
TRIM32 and Malin in Neurological and Neuromuscular Rare Diseases.
Cells
; 10(4)2021 04 06.
Artigo
Inglês
| MEDLINE | ID: mdl-33917450
15.
An online tool for fetal fraction prediction based on direct size distribution analysis of maternal cell-free DNA.
Biotechniques
; 70(2): 81-88, 2021 02.
Artigo
Inglês
| MEDLINE | ID: mdl-33249919
16.
The MID1 gene product in physiology and disease.
Gene
; 747: 144655, 2020 Jul 15.
Artigo
Inglês
| MEDLINE | ID: mdl-32283114
17.
Emerging Roles of the TRIM E3 Ubiquitin Ligases MID1 and MID2 in Cytokinesis.
Front Physiol
; 10: 274, 2019.
Artigo
Inglês
| MEDLINE | ID: mdl-30941058
18.
Analysis of the Zn-Binding Domains of TRIM32, the E3 Ubiquitin Ligase Mutated in Limb Girdle Muscular Dystrophy 2H.
Cells
; 8(3)2019 03 16.
Artigo
Inglês
| MEDLINE | ID: mdl-30884854
19.
A unique missense mutation in the RING domain impairs MID1 E3 ubiquitin ligase activity and localisation and is associated with uncommon Opitz Syndrome-like signs.
Biochim Biophys Acta Mol Basis Dis
; 1870(4): 167126, 2024 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-38508475
20.
Cellular TRIM33 restrains HIV-1 infection by targeting viral integrase for proteasomal degradation.
Nat Commun
; 10(1): 926, 2019 02 25.
Artigo
Inglês
| MEDLINE | ID: mdl-30804369