Detalhe da pesquisa
1.
A common allele of HLA is associated with asymptomatic SARS-CoV-2 infection.
Nature;
620(7972): 128-136, 2023 Aug.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37468623
2.
Neurite outgrowth deficits caused by rare PLXNB1 mutation in pediatric bipolar disorder.
Mol Psychiatry;
28(6): 2525-2539, 2023 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37032361
3.
Postseptic Cognitive Impairment and Expression of APOE in Peripheral Blood: The Cognition After SepsiS (CASS) Observational Pilot Study.
J Intensive Care Med;
36(3): 262-270, 2021 Mar.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31916880
4.
A systemic sclerosis disease model: can inducible pluripotent stem cells fill an unmet need in defining vascular leak?
Rheumatology (Oxford);
62(7): e226-e228, 2023 07 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36575990
5.
Deletion of Glycogen Synthase Kinase 3 Beta Reprograms NK Cell Metabolism.
Cancers (Basel);
15(3)2023 Jan 24.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36765663
6.
Focal adhesion kinase regulates smooth muscle cell recruitment to the developing vasculature.
Arterioscler Thromb Vasc Biol;
31(10): 2193-202, 2011 Oct.
Artigo
em Inglês
| MEDLINE
| ID: mdl-21757658
7.
Mitochondrial calcium uniporter stabilization preserves energetic homeostasis during Complex I impairment.
Nat Commun;
13(1): 2769, 2022 05 19.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35589699
8.
A common allele of HLA mediates asymptomatic SARS-CoV-2 infection.
medRxiv;
2022 Oct 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34031661
9.
Loss of microRNAs in neural crest leads to cardiovascular syndromes resembling human congenital heart defects.
Arterioscler Thromb Vasc Biol;
30(12): 2575-86, 2010 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-20884876
10.
A sonic hedgehog signaling domain in the arterial adventitia supports resident Sca1+ smooth muscle progenitor cells.
Proc Natl Acad Sci U S A;
105(27): 9349-54, 2008 Jul 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-18591670
11.
Generation and Genetic Correction of USH2A c.2299delG Mutation in Patient-Derived Induced Pluripotent Stem Cells.
Genes (Basel);
12(6)2021 05 25.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34070435
12.
The history and geographic distribution of a KCNQ1 atrial fibrillation risk allele.
Nat Commun;
12(1): 6442, 2021 11 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34750360
13.
Genetic Mapping of a new Hippo allele, HpoN.1.2, in Drosophila melanogaster.
MicroPubl Biol;
20212021 Apr 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33851093
14.
Relationship of lipoprotein-associated phospholipase A2 and oxidized low density lipoprotein in carotid atherosclerosis.
J Lipid Res;
50(9): 1735-43, 2009 Sep.
Artigo
em Inglês
| MEDLINE
| ID: mdl-19359705
15.
Nkx2-5 mutation causes anatomic hypoplasia of the cardiac conduction system.
J Clin Invest;
113(8): 1130-7, 2004 Apr.
Artigo
em Inglês
| MEDLINE
| ID: mdl-15085192
16.
Author Correction: Mitochondrial calcium uniporter stabilization preserves energetic homeostasis during Complex I impairment.
Nat Commun;
13(1): 3532, 2022 Jun 20.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35725853
17.
Transgenic mice overexpressing mutant PRKAG2 define the cause of Wolff-Parkinson-White syndrome in glycogen storage cardiomyopathy.
Circulation;
107(22): 2850-6, 2003 Jun 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-12782567
18.
Electrophysiologic characterization and postnatal development of ventricular pre-excitation in a mouse model of cardiac hypertrophy and Wolff-Parkinson-White syndrome.
J Am Coll Cardiol;
42(5): 942-51, 2003 Sep 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-12957447
19.
Implications of ventricular arrhythmia vulnerability during murine electrophysiology studies.
Physiol Genomics;
15(1): 84-91, 2003 Sep 29.
Artigo
em Inglês
| MEDLINE
| ID: mdl-12888626
20.
Function follows form: cardiac conduction system defects in Nkx2-5 mutation.
Anat Rec A Discov Mol Cell Evol Biol;
280(2): 966-72, 2004 Oct.
Artigo
em Inglês
| MEDLINE
| ID: mdl-15368343