Detalhe da pesquisa
1.
The rRNA m6A methyltransferase METTL5 is involved in pluripotency and developmental programs.
Genes Dev
; 34(9-10): 715-729, 2020 05 01.
Artigo
Inglês
| MEDLINE | ID: mdl-32217665
2.
Insights into energy balance dysregulation from a mouse model of methylmalonic aciduria.
Hum Mol Genet
; 32(17): 2717-2734, 2023 08 26.
Artigo
Inglês
| MEDLINE | ID: mdl-37369025
3.
Mass spectrometry-based draft of the mouse proteome.
Nat Methods
; 19(7): 803-811, 2022 07.
Artigo
Inglês
| MEDLINE | ID: mdl-35710609
4.
Mice lacking the mitochondrial exonuclease MGME1 develop inflammatory kidney disease with glomerular dysfunction.
PLoS Genet
; 18(5): e1010190, 2022 05.
Artigo
Inglês
| MEDLINE | ID: mdl-35533204
5.
Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT).
Kidney Int
; 105(4): 844-864, 2024 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-38154558
6.
A humanized version of Foxp2 affects cortico-basal ganglia circuits in mice.
Cell
; 137(5): 961-71, 2009 May 29.
Artigo
Inglês
| MEDLINE | ID: mdl-19490899
7.
Knockout mouse models as a resource for the study of rare diseases.
Mamm Genome
; 34(2): 244-261, 2023 06.
Artigo
Inglês
| MEDLINE | ID: mdl-37160609
8.
Biallelic loss-of-function variants in RABGAP1 cause a novel neurodevelopmental syndrome.
Genet Med
; 24(11): 2399-2407, 2022 11.
Artigo
Inglês
| MEDLINE | ID: mdl-36083289
9.
A comprehensive phenotypic characterization of a whole-body Wdr45 knock-out mouse.
Mamm Genome
; 32(5): 332-349, 2021 10.
Artigo
Inglês
| MEDLINE | ID: mdl-34043061
10.
A comprehensive and comparative phenotypic analysis of the collaborative founder strains identifies new and known phenotypes.
Mamm Genome
; 31(1-2): 30-48, 2020 02.
Artigo
Inglês
| MEDLINE | ID: mdl-32060626
11.
Low catalytic activity is insufficient to induce disease pathology in triosephosphate isomerase deficiency.
J Inherit Metab Dis
; 42(5): 839-849, 2019 09.
Artigo
Inglês
| MEDLINE | ID: mdl-31111503
12.
Standardized, systemic phenotypic analysis reveals kidney dysfunction as main alteration of Kctd1 I27N mutant mice.
J Biomed Sci
; 24(1): 57, 2017 Aug 17.
Artigo
Inglês
| MEDLINE | ID: mdl-28818080
13.
Peptidase inhibitor 16 is a membrane-tethered regulator of chemerin processing in the myocardium.
J Mol Cell Cardiol
; 99: 57-64, 2016 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-27539859
14.
MiR-34a deficiency accelerates medulloblastoma formation in vivo.
Int J Cancer
; 136(10): 2293-303, 2015 May 15.
Artigo
Inglês
| MEDLINE | ID: mdl-25348795
15.
An ENU mutagenesis-derived mouse model with a dominant Jak1 mutation resembling phenotypes of systemic autoimmune disease.
Am J Pathol
; 183(2): 352-68, 2013 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-23791841
16.
Missing-in-metastasis MIM/MTSS1 promotes actin assembly at intercellular junctions and is required for integrity of kidney epithelia.
J Cell Sci
; 124(Pt 8): 1245-55, 2011 Apr 15.
Artigo
Inglês
| MEDLINE | ID: mdl-21406566
17.
Srgap3â»/â» mice present a neurodevelopmental disorder with schizophrenia-related intermediate phenotypes.
FASEB J
; 26(11): 4418-28, 2012 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-22820399
18.
AOX delays the onset of the lethal phenotype in a mouse model of Uqcrh (complex III) disease.
Biochim Biophys Acta Mol Basis Dis
; 1869(7): 166760, 2023 10.
Artigo
Inglês
| MEDLINE | ID: mdl-37230398
19.
Implication of FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT).
medRxiv
; 2023 Mar 22.
Artigo
Inglês
| MEDLINE | ID: mdl-36993625
20.
Requirement of the RNA-editing enzyme ADAR2 for normal physiology in mice.
J Biol Chem
; 286(21): 18614-22, 2011 May 27.
Artigo
Inglês
| MEDLINE | ID: mdl-21467037