Detalhe da pesquisa
1.
Chemical Hybridization of Glucagon and Thyroid Hormone Optimizes Therapeutic Impact for Metabolic Disease.
Cell
; 167(3): 843-857.e14, 2016 Oct 20.
Artigo
Inglês
| MEDLINE | ID: mdl-27720451
2.
Single-cell, whole-embryo phenotyping of mammalian developmental disorders.
Nature
; 623(7988): 772-781, 2023 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-37968388
3.
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
4.
Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing.
Hum Mol Genet
; 32(8): 1266-1275, 2023 04 06.
Artigo
Inglês
| MEDLINE | ID: mdl-36349687
5.
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
6.
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
7.
TRPS1 maintains luminal progenitors in the mammary gland by repressing SRF/MRTF activity.
Breast Cancer Res
; 26(1): 74, 2024 May 03.
Artigo
Inglês
| MEDLINE | ID: mdl-38702730
8.
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
9.
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
10.
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
11.
Knockout of the Complex III subunit Uqcrh causes bioenergetic impairment and cardiac contractile dysfunction.
Mamm Genome
; 34(2): 229-243, 2023 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-36565314
12.
A review of standardized high-throughput cardiovascular phenotyping with a link to metabolism in mice.
Mamm Genome
; 34(2): 107-122, 2023 06.
Artigo
Inglês
| MEDLINE | ID: mdl-37326672
13.
Echo2Pheno: a deep-learning application to uncover echocardiographic phenotypes in conscious mice.
Mamm Genome
; 34(2): 200-215, 2023 06.
Artigo
Inglês
| MEDLINE | ID: mdl-37221250
14.
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
15.
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
Inglês
| MEDLINE | ID: mdl-37294348
16.
Aqp5-/- mice exhibit reduced maximal body O2 consumption under cold exposure, normal pulmonary gas exchange, and impaired formation of brown adipose tissue.
Am J Physiol Regul Integr Comp Physiol
; 324(1): R109-R119, 2023 01 01.
Artigo
Inglês
| MEDLINE | ID: mdl-36409022
17.
RNA editing of Filamin A pre-mRNA regulates vascular contraction and diastolic blood pressure.
EMBO J
; 37(19)2018 10 01.
Artigo
Inglês
| MEDLINE | ID: mdl-30087110
18.
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
19.
N471D WASH complex subunit strumpellin knock-in mice display mild motor and cardiac abnormalities and BPTF and KLHL11 dysregulation in brain tissue.
Neuropathol Appl Neurobiol
; 48(1): e12750, 2022 02.
Artigo
Inglês
| MEDLINE | ID: mdl-34312900
20.
High-throughput discovery of novel developmental phenotypes.
Nature
; 537(7621): 508-514, 2016 09 22.
Artigo
Inglês
| MEDLINE | ID: mdl-27626380