Detalhe da pesquisa
1.
Ablation of lysophosphatidic acid receptor 1 attenuates hypertrophic cardiomyopathy in a mouse model.
Proc Natl Acad Sci U S A
; 119(28): e2204174119, 2022 07 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-35787042
2.
Impaired lymphatic contraction associated with immunosuppression.
Proc Natl Acad Sci U S A
; 108(46): 18784-9, 2011 Nov 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-22065738
3.
Surfactant protein-C chromatin-bound green fluorescence protein reporter mice reveal heterogeneity of surfactant protein C-expressing lung cells.
Am J Respir Cell Mol Biol
; 48(3): 288-98, 2013 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-23204392
4.
Efficient in vivo genome editing prevents hypertrophic cardiomyopathy in mice.
Nat Med
; 29(2): 412-421, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36797483
5.
Eya4-deficient mice are a model for heritable otitis media.
J Clin Invest
; 118(2): 651-8, 2008 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-18219393
6.
LAMP2 Cardiomyopathy: Consequences of Impaired Autophagy in the Heart.
J Am Heart Assoc
; 10(17): e018829, 2021 09 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34459252
7.
Calsequestrin 2 (CASQ2) mutations increase expression of calreticulin and ryanodine receptors, causing catecholaminergic polymorphic ventricular tachycardia.
J Clin Invest
; 117(7): 1814-23, 2007 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-17607358
8.
BET bromodomain proteins regulate transcriptional reprogramming in genetic dilated cardiomyopathy.
JCI Insight
; 5(15)2020 08 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32603312
9.
Lamin A/C haploinsufficiency causes dilated cardiomyopathy and apoptosis-triggered cardiac conduction system disease.
J Mol Cell Cardiol
; 44(2): 293-303, 2008 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-18182166
10.
CRISPR/Cas9-Mediated Fluorescent Tagging of Endogenous Proteins in Human Pluripotent Stem Cells.
Curr Protoc Hum Genet
; 96: 21.11.1-21.11.20, 2018 01 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-29364519
11.
Molecular profiling of dilated cardiomyopathy that progresses to heart failure.
JCI Insight
; 1(6)2016 May 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-27239561
12.
5'RNA-Seq identifies Fhl1 as a genetic modifier in cardiomyopathy.
J Clin Invest
; 124(3): 1364-70, 2014 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-24509080
13.
Rapamycin reverses hypertrophic cardiomyopathy in a mouse model of LEOPARD syndrome-associated PTPN11 mutation.
J Clin Invest
; 121(3): 1026-43, 2011 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-21339643
14.
The role of cardiac troponin T quantity and function in cardiac development and dilated cardiomyopathy.
PLoS One
; 3(7): e2642, 2008 Jul 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-18612386
15.
Regulation of tendon differentiation by scleraxis distinguishes force-transmitting tendons from muscle-anchoring tendons.
Development
; 134(14): 2697-708, 2007 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-17567668
16.
Wnt9a signaling is required for joint integrity and regulation of Ihh during chondrogenesis.
Development
; 133(15): 3039-49, 2006 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-16818445
17.
Cardiac myosin missense mutations cause dilated cardiomyopathy in mouse models and depress molecular motor function.
Proc Natl Acad Sci U S A
; 103(39): 14525-30, 2006 Sep 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-16983074
18.
Transgenic mouse colony management.
Curr Protoc Mol Biol
; Chapter 23: Unit 23.10, 2005 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-18265361
19.
Transgenic mouse production by zygote injection.
Curr Protoc Mol Biol
; Chapter 23: Unit 23.9, 2004 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-18265349
20.
Mouse colony management.
Curr Protoc Mol Biol
; Chapter 23: Unit 23.8, 2002 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-18265310