Detalhe da pesquisa
1.
A Transcriptomic Meta-Analysis Shows Lipid Metabolism Dysregulation as an Early Pathological Mechanism in the Spinal Cord of SOD1 Mice.
Int J Mol Sci
; 22(17)2021 Sep 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34502460
2.
A genetic modifier suggests that endurance exercise exacerbates Huntington's disease.
Hum Mol Genet
; 27(10): 1723-1731, 2018 05 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-29509900
3.
A mutation in Nischarin causes otitis media via LIMK1 and NF-κB pathways.
PLoS Genet
; 13(8): e1006969, 2017 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-28806779
4.
Genetic Analysis Reveals a Hierarchy of Interactions between Polycystin-Encoding Genes and Genes Controlling Cilia Function during Left-Right Determination.
PLoS Genet
; 12(6): e1006070, 2016 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27272319
5.
Symptomatic secondary syphilis: empirical antimicrobial treatment or await microbiology?
Sex Health
; 16(6): 598-599, 2019 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31665617
6.
Chronic Kidney Disease Risk in African and Caribbean Populations With HIV.
J Infect Dis
; 218(11): 1767-1772, 2018 10 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-29982487
7.
ATMIN is a transcriptional regulator of both lung morphogenesis and ciliogenesis.
Development
; 141(20): 3966-77, 2014 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25294941
8.
Clinical characteristics and outcomes of HIV-associated immune complex kidney disease.
Nephrol Dial Transplant
; 31(12): 2099-2107, 2016 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-26786550
9.
Probing Cancer Cell Metabolism Using NMR Spectroscopy.
Adv Exp Med Biol
; 899: 89-111, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27325263
10.
Myofibrillar myopathy caused by a mutation in the motor domain of mouse MyHC IIb.
Hum Mol Genet
; 21(8): 1706-24, 2012 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-22199023
11.
MicroRNAs 296 and 298 are imprinted and part of the GNAS/Gnas cluster and miR-296 targets IKBKE and Tmed9.
RNA
; 18(1): 135-44, 2012 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-22114321
12.
HIF-VEGF pathways are critical for chronic otitis media in Junbo and Jeff mouse mutants.
PLoS Genet
; 7(10): e1002336, 2011 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-22028672
13.
A mutation in the mitochondrial fission gene Dnm1l leads to cardiomyopathy.
PLoS Genet
; 6(6): e1001000, 2010 Jun 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-20585624
14.
Loss of mitogen-activated protein kinase kinase kinase 4 (MAP3K4) reveals a requirement for MAPK signalling in mouse sex determination.
PLoS Biol
; 7(9): e1000196, 2009 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-19753101
15.
Mouse hitchhiker mutants have spina bifida, dorso-ventral patterning defects and polydactyly: identification of Tulp3 as a novel negative regulator of the Sonic hedgehog pathway.
Hum Mol Genet
; 18(10): 1719-39, 2009 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-19223390
16.
Upregulation of PKD1L2 provokes a complex neuromuscular disease in the mouse.
Hum Mol Genet
; 18(19): 3553-66, 2009 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-19578180
17.
Zfhx3-mediated genetic ablation of the SCN abolishes light entrainable circadian activity while sparing food anticipatory activity.
iScience
; 24(10): 103142, 2021 Oct 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-34632336
18.
Ciliary exclusion of Polycystin-2 promotes kidney cystogenesis in an autosomal dominant polycystic kidney disease model.
Nat Commun
; 10(1): 4072, 2019 09 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31492868
19.
Transcript Analysis Reveals a Hypoxic Inflammatory Environment in Human Chronic Otitis Media With Effusion.
Front Genet
; 10: 1327, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-32153623
20.
Clarin-2 is essential for hearing by maintaining stereocilia integrity and function.
EMBO Mol Med
; 11(9): e10288, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-31448880