Detalhe da pesquisa
1.
Pleiotropic role of TRAF7 in skull-base meningiomas and congenital heart disease.
Proc Natl Acad Sci U S A
; 120(16): e2214997120, 2023 04 18.
Artigo
Inglês
| MEDLINE | ID: mdl-37043537
2.
Reply to Pisan et al.: Pathogenicity of inherited TRAF7 mutations in congenital heart disease.
Proc Natl Acad Sci U S A
; 121(12): e2319578121, 2024 Mar 19.
Artigo
Inglês
| MEDLINE | ID: mdl-38466853
3.
Cerebrovascular disorders associated with genetic lesions.
Cell Mol Life Sci
; 76(2): 283-300, 2019 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-30327838
4.
Combined HMG-COA reductase and prenylation inhibition in treatment of CCM.
Proc Natl Acad Sci U S A
; 114(21): 5503-5508, 2017 05 23.
Artigo
Inglês
| MEDLINE | ID: mdl-28500274
5.
Ccm3, a gene associated with cerebral cavernous malformations, is required for neuronal migration.
Development
; 141(6): 1404-15, 2014 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-24595293
6.
International Trends in Adverse Drug Event-Related Mortality from 2001 to 2019: An Analysis of the World Health Organization Mortality Database from 54 Countries.
Drug Saf
; 47(3): 237-249, 2024 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-38133735
7.
Altered Expression of Several Molecular Mediators of Cerebrospinal Fluid Production in Hyp Mice.
J Endocr Soc
; 7(4): bvad022, 2023 Feb 09.
Artigo
Inglês
| MEDLINE | ID: mdl-36819458
8.
Super-enhancer hijacking drives ectopic expression of hedgehog pathway ligands in meningiomas.
Nat Commun
; 14(1): 6279, 2023 10 07.
Artigo
Inglês
| MEDLINE | ID: mdl-37805627
9.
Polycystin-2 is an intracellular calcium release channel.
Nat Cell Biol
; 4(3): 191-7, 2002 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-11854751
10.
ATF3 protects against renal ischemia-reperfusion injury.
J Am Soc Nephrol
; 19(2): 217-24, 2008 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-18235102
11.
Functional synergy between cholecystokinin receptors CCKAR and CCKBR in mammalian brain development.
PLoS One
; 10(4): e0124295, 2015.
Artigo
Inglês
| MEDLINE | ID: mdl-25875176
12.
Homozygous loss of DIAPH1 is a novel cause of microcephaly in humans.
Eur J Hum Genet
; 23(2): 165-72, 2015 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-24781755
13.
Mutations in KATNB1 cause complex cerebral malformations by disrupting asymmetrically dividing neural progenitors.
Neuron
; 84(6): 1226-39, 2014 Dec 17.
Artigo
Inglês
| MEDLINE | ID: mdl-25521378
14.
Mutations in KATNB1 Cause Complex Cerebral Malformations by Disrupting Asymmetrically Dividing Neural Progenitors.
Neuron
; 85(1): 228, 2015 Jan 07.
Artigo
Inglês
| MEDLINE | ID: mdl-29654772
15.
CD2AP expression in a renal ischemia/reperfusion injury model and analysis of its related genes using overexpression and RNA interference technique.
Am J Nephrol
; 25(4): 373-81, 2005.
Artigo
Inglês
| MEDLINE | ID: mdl-16088078
16.
Klotho reduces apoptosis in experimental ischaemic acute renal failure.
Nephrol Dial Transplant
; 20(12): 2636-45, 2005 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-16204278
17.
Trans-heterozygous Pkd1 and Pkd2 mutations modify expression of polycystic kidney disease.
Hum Mol Genet
; 11(16): 1845-54, 2002 Aug 01.
Artigo
Inglês
| MEDLINE | ID: mdl-12140187