Detalhe da pesquisa
1.
An Improved Method for Growing Primary Neurons on Electron Microscopy Grids Co-Cultured with Astrocytes.
Int J Mol Sci
; 24(20)2023 Oct 14.
Artigo
Inglês
| MEDLINE | ID: mdl-37894872
2.
Nuclear accumulation of myocyte muscle LIM protein is regulated by heme oxygenase 1 and correlates with cardiac function in the transition to failure.
J Physiol
; 594(12): 3287-305, 2016 06 15.
Artigo
Inglês
| MEDLINE | ID: mdl-26847743
3.
Scribble is required for normal epithelial cell-cell contacts and lumen morphogenesis in the mammalian lung.
Dev Biol
; 373(2): 267-80, 2013 Jan 15.
Artigo
Inglês
| MEDLINE | ID: mdl-23195221
4.
The mouse Wnt/PCP protein Vangl2 is necessary for migration of facial branchiomotor neurons, and functions independently of Dishevelled.
Dev Biol
; 369(2): 211-22, 2012 Sep 15.
Artigo
Inglês
| MEDLINE | ID: mdl-22771245
5.
Modulation of stretch-induced myocyte remodeling and gene expression by nitric oxide: a novel role for lipoma preferred partner in myofibrillogenesis.
Am J Physiol Heart Circ Physiol
; 304(10): H1302-13, 2013 May 15.
Artigo
Inglês
| MEDLINE | ID: mdl-23504181
6.
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
Inglês
| MEDLINE | ID: mdl-19223390
7.
The novel mouse mutant, chuzhoi, has disruption of Ptk7 protein and exhibits defects in neural tube, heart and lung development and abnormal planar cell polarity in the ear.
BMC Dev Biol
; 10: 87, 2010 Aug 12.
Artigo
Inglês
| MEDLINE | ID: mdl-20704721
8.
Mylk3 null C57BL/6N mice develop cardiomyopathy, whereas Nnt null C57BL/6J mice do not.
Life Sci Alliance
; 3(4)2020 04.
Artigo
Inglês
| MEDLINE | ID: mdl-32213617
9.
The exon junction complex senses energetic stress and regulates contractility and cell architecture in cardiac myocytes.
Biosci Rep
; 37(4)2017 08 31.
Artigo
Inglês
| MEDLINE | ID: mdl-28566540
10.
N-ethyl-N-nitrosourea-Induced Adaptor Protein 2 Sigma Subunit 1 (Ap2s1) Mutations Establish Ap2s1 Loss-of-Function Mice.
JBMR Plus
; 1(1): 3-15, 2017 May 02.
Artigo
Inglês
| MEDLINE | ID: mdl-29479578
11.
Cinacalcet corrects hypercalcemia in mice with an inactivating Gα11 mutation.
JCI Insight
; 2(20)2017 10 19.
Artigo
Inglês
| MEDLINE | ID: mdl-29046478
12.
Gα11 mutation in mice causes hypocalcemia rectifiable by calcilytic therapy.
JCI Insight
; 2(3): e91103, 2017 02 09.
Artigo
Inglês
| MEDLINE | ID: mdl-28194447
13.
Genetic interactions between planar cell polarity genes cause diverse neural tube defects in mice.
Dis Model Mech
; 7(10): 1153-63, 2014 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-25128525
14.
Dissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screen.
Proc Natl Acad Sci U S A
; 102(35): 12477-82, 2005 Aug 30.
Artigo
Inglês
| MEDLINE | ID: mdl-16109771