Detalhe da pesquisa
1.
A missense mutation in zinc finger homeobox-3 (ZFHX3) impedes growth and alters metabolism and hypothalamic gene expression in mice.
FASEB J;
37(10): e23189, 2023 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37713040
2.
Cleft palate and minor metabolic disturbances in a mouse global Arl15 gene knockout.
FASEB J;
37(11): e23211, 2023 11.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37773757
3.
Loss of Bardet-Biedl syndrome proteins causes synaptic aberrations in principal neurons.
PLoS Biol;
17(9): e3000414, 2019 09.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31479441
4.
Correction: Loss of Bardet-Biedl syndrome proteins causes synaptic aberrations in principal neurons.
PLoS Biol;
17(10): e3000520, 2019 Oct.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31593567
5.
A novel mutation in the mouse Pcsk1 gene showing obesity and diabetes.
Mamm Genome;
31(1-2): 17-29, 2020 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31974728
6.
Novel mutations in human and mouse SCN4A implicate AMPK in myotonia and periodic paralysis.
Brain;
137(Pt 12): 3171-85, 2014 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25348630
7.
Leptin haploinsufficiency exerts sex-dependent partial protection in SOD1G93A mice by reducing inflammatory pathways in the adipose tissue.
Sci Rep;
14(1): 2671, 2024 02 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38302474
8.
Expression of an activating mutation in the gene encoding the KATP channel subunit Kir6.2 in mouse pancreatic beta cells recapitulates neonatal diabetes.
J Clin Invest;
119(1): 80-90, 2009 Jan.
Artigo
em Inglês
| MEDLINE
| ID: mdl-19065048
9.
A Wars2 mutant mouse shows a sex and diet specific change in fat distribution, reduced food intake and depot-specific upregulation of WAT browning.
Front Physiol;
13: 953199, 2022.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36091365
10.
AKR1D1 knockout mice develop a sex-dependent metabolic phenotype.
J Endocrinol;
253(3): 97-113, 2022 04 13.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35318963
11.
Palmitoylated small GTPase ARL15 is translocated within Golgi network during adipogenesis.
Biol Open;
10(12)2021 12 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34779483
12.
The KCNJ11-E23K Gene Variant Hastens Diabetes Progression by Impairing Glucose-Induced Insulin Secretion.
Diabetes;
70(5): 1145-1156, 2021 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33568422
13.
Linking the FTO obesity rs1421085 variant circuitry to cellular, metabolic, and organismal phenotypes in vivo.
Sci Adv;
7(30)2021 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34290091
14.
A lead candidate functional single nucleotide polymorphism within the WARS2 gene associated with waist-hip-ratio does not alter RNA stability.
Biochim Biophys Acta Gene Regul Mech;
1863(11): 194640, 2020 11.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33007465
15.
Monitoring type 2 diabetes from volatile faecal metabolome in Cushing's syndrome and single Afmid mouse models via a longitudinal study.
Sci Rep;
9(1): 18779, 2019 12 11.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31827172
16.
The development of a high throughput drug-responsive model of white adipose tissue comprising adipogenic 3T3-L1 cells in a 3D matrix.
Biofabrication;
12(1): 015018, 2019 12 11.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31715591
17.
An N-Ethyl-N-Nitrosourea (ENU)-Induced Tyr265Stop Mutation of the DNA Polymerase Accessory Subunit Gamma 2 (Polg2) Is Associated With Renal Calcification in Mice.
J Bone Miner Res;
34(3): 497-507, 2019 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30395686
18.
Mice with a Brd4 Mutation Represent a New Model of Nephrocalcinosis.
J Bone Miner Res;
34(7): 1324-1335, 2019 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30830987
19.
A Wars2 Mutant Mouse Model Displays OXPHOS Deficiencies and Activation of Tissue-Specific Stress Response Pathways.
Cell Rep;
25(12): 3315-3328.e6, 2018 12 18.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30566859
20.
A mouse model for inherited renal fibrosis associated with endoplasmic reticulum stress.
Dis Model Mech;
10(6): 773-786, 2017 06 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28325753