Detalhe da pesquisa
1.
A humanized version of Foxp2 affects cortico-basal ganglia circuits in mice.
Cell
; 137(5): 961-71, 2009 May 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-19490899
2.
Murine tissue factor disulfide mutation causes a bleeding phenotype with sex specific organ pathology and lethality.
Haematologica
; 105(10): 2484-2495, 2020 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33054088
3.
MFAP4 Promotes Vascular Smooth Muscle Migration, Proliferation and Accelerates Neointima Formation.
Arterioscler Thromb Vasc Biol
; 36(1): 122-33, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26564819
4.
Cardiopulmonary dysfunction in the Osteogenesis imperfecta mouse model Aga2 and human patients are caused by bone-independent mechanisms.
Hum Mol Genet
; 21(16): 3535-45, 2012 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-22589248
5.
Standardized, systemic phenotypic analysis of Slc12a1I299F mutant mice.
J Biomed Sci
; 21: 68, 2014 Aug 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-25084970
6.
Cytochrome c oxidase subunit 4 isoform 2-knockout mice show reduced enzyme activity, airway hyporeactivity, and lung pathology.
FASEB J
; 26(9): 3916-30, 2012 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-22730437
7.
Post-stroke inhibition of induced NADPH oxidase type 4 prevents oxidative stress and neurodegeneration.
PLoS Biol
; 8(9)2010 Sep 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-20877715
8.
Requirement of the RNA-editing enzyme ADAR2 for normal physiology in mice.
J Biol Chem
; 286(21): 18614-22, 2011 May 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-21467037
9.
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
10.
11.
Mutation of the Na(+)-K(+)-2Cl(-) cotransporter NKCC2 in mice is associated with severe polyuria and a urea-selective concentrating defect without hyperreninemia.
Am J Physiol Renal Physiol
; 298(6): F1405-15, 2010 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-20219826
12.
Novel missense mutation of uromodulin in mice causes renal dysfunction with alterations in urea handling, energy, and bone metabolism.
Am J Physiol Renal Physiol
; 297(5): F1391-8, 2009 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-19692485
13.
Systemic first-line phenotyping.
Methods Mol Biol
; 530: 463-509, 2009.
Artigo
em Inglês
| MEDLINE | ID: mdl-19266331
14.
Pleiotropic effects in Eya3 knockout mice.
BMC Dev Biol
; 8: 118, 2008 Dec 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-19102749
15.
"Sighted C3H" mice--a tool for analysing the influence of vision on mouse behaviour?
Front Biosci
; 13: 5810-23, 2008 May 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-18508624
16.
Atrial natriuretic peptide and osteopontin are useful markers of cardiac disorders in mice.
Comp Med
; 57(6): 546-53, 2007 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-18246866
17.
Heart-Specific Knockout of the Mitochondrial Thioredoxin Reductase (Txnrd2) Induces Metabolic and Contractile Dysfunction in the Aging Myocardium.
J Am Heart Assoc
; 4(7)2015 Jul 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-26199228
18.
MTO1-deficient mouse model mirrors the human phenotype showing complex I defect and cardiomyopathy.
PLoS One
; 9(12): e114918, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-25506927
19.
Standardized, systemic phenotypic analysis of Umod(C93F) and Umod(A227T) mutant mice.
PLoS One
; 8(10): e78337, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-24205203
20.
Large-scale phenotyping of an accurate genetic mouse model of JNCL identifies novel early pathology outside the central nervous system.
PLoS One
; 7(6): e38310, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22701626