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
em Inglês
| MEDLINE | ID: mdl-32217665
2.
Monoallelic variation in DHX9, the gene encoding the DExH-box helicase DHX9, underlies neurodevelopment disorders and Charcot-Marie-Tooth disease.
Am J Hum Genet
; 110(8): 1394-1413, 2023 08 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-37467750
3.
Roquin Suppresses the PI3K-mTOR Signaling Pathway to Inhibit T Helper Cell Differentiation and Conversion of Treg to Tfr Cells.
Immunity
; 47(6): 1067-1082.e12, 2017 12 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-29246441
4.
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
em Inglês
| MEDLINE | ID: mdl-38154558
5.
A review of standardized high-throughput cardiovascular phenotyping with a link to metabolism in mice.
Mamm Genome
; 34(2): 107-122, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-37326672
6.
Knockout mouse models as a resource for the study of rare diseases.
Mamm Genome
; 34(2): 244-261, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-37160609
7.
Comprehensive ECG reference intervals in C57BL/6N substrains provide a generalizable guide for cardiac electrophysiology studies in mice.
Mamm Genome
; 34(2): 180-199, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-37294348
8.
Corrigendum: High-throughput discovery of novel developmental phenotypes.
Nature
; 551(7680): 398, 2017 11 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-29144450
9.
Susceptibility to diet-induced obesity at thermoneutral conditions is independent of UCP1.
Am J Physiol Endocrinol Metab
; 322(2): E85-E100, 2022 02 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34927460
10.
Biallelic loss-of-function variants in RABGAP1 cause a novel neurodevelopmental syndrome.
Genet Med
; 24(11): 2399-2407, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-36083289
11.
High-throughput discovery of novel developmental phenotypes.
Nature
; 537(7621): 508-514, 2016 09 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-27626380
12.
Dexamethasone treatment alters insulin, leptin, and adiponectin levels in male mice as observed in DIO but does not lead to alterations of metabolic phenotypes in the offspring.
Mamm Genome
; 27(1-2): 17-28, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26662513
13.
Viable Ednra Y129F mice feature human mandibulofacial dysostosis with alopecia (MFDA) syndrome due to the homologue mutation.
Mamm Genome
; 27(11-12): 587-598, 2016 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-27671791
14.
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
em Inglês
| MEDLINE | ID: mdl-37230398
15.
Deletion of SERF2 in mice delays embryonic development and alters amyloid deposit structure in the brain.
Life Sci Alliance
; 6(7)2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37130781
16.
Implication of FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT).
medRxiv
; 2023 Mar 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-36993625
17.
Overview of new developments in and the future of cryopreservation in the laboratory mouse.
Mamm Genome
; 23(9-10): 572-9, 2012 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-22936001
18.
Mouse large-scale phenotyping initiatives: overview of the European Mouse Disease Clinic (EUMODIC) and of the Wellcome Trust Sanger Institute Mouse Genetics Project.
Mamm Genome
; 23(9-10): 600-10, 2012 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-22961258
19.
Innovations in phenotyping of mouse models in the German Mouse Clinic.
Mamm Genome
; 23(9-10): 611-22, 2012 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-22926221
20.
The mammalian gene function resource: the International Knockout Mouse Consortium.
Mamm Genome
; 23(9-10): 580-6, 2012 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-22968824