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.
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
3.
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
4.
A systematic review of the development and application of home cage monitoring in laboratory mice and rats.
BMC Biol
; 21(1): 256, 2023 11 13.
Artigo
Inglês
| MEDLINE | ID: mdl-37953247
5.
Recommendations for robust and reproducible preclinical research in personalised medicine.
BMC Med
; 21(1): 14, 2023 01 08.
Artigo
Inglês
| MEDLINE | ID: mdl-36617553
6.
A rationale for considering heart/brain axis control in neuropsychiatric disease.
Mamm Genome
; 34(2): 331-350, 2023 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-36538124
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.
A Pathophysiological Intersection of Diabetes and Alzheimer's Disease.
Int J Mol Sci
; 23(19)2022 Sep 30.
Artigo
Inglês
| MEDLINE | ID: mdl-36232867
9.
Laboratory mouse housing conditions can be improved using common environmental enrichment without compromising data.
PLoS Biol
; 16(4): e2005019, 2018 04.
Artigo
Inglês
| MEDLINE | ID: mdl-29659570
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.
Interplay between H1 and HMGN epigenetically regulates OLIG1&2 expression and oligodendrocyte differentiation.
Nucleic Acids Res
; 45(6): 3031-3045, 2017 04 07.
Artigo
Inglês
| MEDLINE | ID: mdl-27923998
13.
Aberrant methylation of tRNAs links cellular stress to neuro-developmental disorders.
EMBO J
; 33(18): 2020-39, 2014 Sep 17.
Artigo
Inglês
| MEDLINE | ID: mdl-25063673
14.
Lifetime study in mice after acute low-dose ionizing radiation: a multifactorial study with special focus on cataract risk.
Radiat Environ Biophys
; 57(2): 99-113, 2018 05.
Artigo
Inglês
| MEDLINE | ID: mdl-29327260
15.
Restless legs syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon.
Genome Res
; 24(4): 592-603, 2014 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-24642863
16.
Spinal poly-GA inclusions in a C9orf72 mouse model trigger motor deficits and inflammation without neuron loss.
Acta Neuropathol
; 134(2): 241-254, 2017 08.
Artigo
Inglês
| MEDLINE | ID: mdl-28409281
17.
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
18.
Mitochondrial dysfunction and decrease in body weight of a transgenic knock-in mouse model for TDP-43.
J Biol Chem
; 289(15): 10769-10784, 2014 Apr 11.
Artigo
Inglês
| MEDLINE | ID: mdl-24515116
19.
MiR-34a deficiency accelerates medulloblastoma formation in vivo.
Int J Cancer
; 136(10): 2293-303, 2015 May 15.
Artigo
Inglês
| MEDLINE | ID: mdl-25348795
20.
Neurobeachin, a regulator of synaptic protein targeting, is associated with body fat mass and feeding behavior in mice and body-mass index in humans.
PLoS Genet
; 8(3): e1002568, 2012.
Artigo
Inglês
| MEDLINE | ID: mdl-22438821