Detalhe da pesquisa
1.
Ascribing novel functions to the sarcomeric protein, myosin binding protein H (MyBPH) in cardiac sarcomere contraction.
Exp Cell Res
; 331(2): 338-51, 2015 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25449695
2.
Myomegalin is a novel A-kinase anchoring protein involved in the phosphorylation of cardiac myosin binding protein C.
BMC Cell Biol
; 12: 18, 2011 May 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-21569246
3.
Investigating SAPAP3 variants in the etiology of obsessive-compulsive disorder and trichotillomania in the South African white population.
Compr Psychiatry
; 52(2): 181-7, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21295225
4.
The KCNE genes in hypertrophic cardiomyopathy: a candidate gene study.
J Negat Results Biomed
; 10: 12, 2011 Oct 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-21967835
5.
The role of the brain-derived neurotrophic factor (BDNF) val66met variant in the phenotypic expression of obsessive-compulsive disorder (OCD).
Am J Med Genet B Neuropsychiatr Genet
; 150B(8): 1050-62, 2009 Dec 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-19219856
6.
Troponin T and beta-myosin mutations have distinct cardiac functional effects in hypertrophic cardiomyopathy patients without hypertrophy.
Cardiovasc Res
; 77(4): 687-94, 2008 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-18029407
7.
Genetic variation in angiotensin-converting enzyme 2 gene is associated with extent of left ventricular hypertrophy in hypertrophic cardiomyopathy.
Hum Genet
; 124(1): 57-61, 2008 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-18560893
8.
Investigating the role of the brain-derived neurotrophic factor (BDNF) val66met variant in obsessive-compulsive disorder (OCD).
World J Biol Psychiatry
; 9(2): 126-34, 2008.
Artigo
em Inglês
| MEDLINE | ID: mdl-17853300
9.
Cluster analysis of obsessive-compulsive symptomatology: identifying obsessive-compulsive disorder subtypes.
Isr J Psychiatry Relat Sci
; 45(3): 164-76, 2008.
Artigo
em Inglês
| MEDLINE | ID: mdl-19398820
10.
Investigating the possible effects of trauma experiences and 5-HTT on the dissociative experiences of patients with OCD using path analysis and multiple regression.
Neuropsychobiology
; 56(1): 6-13, 2007.
Artigo
em Inglês
| MEDLINE | ID: mdl-17943026
11.
Genetic correlates in trichotillomania--A case-control association study in the South African Caucasian population.
Isr J Psychiatry Relat Sci
; 43(2): 93-101, 2006.
Artigo
em Inglês
| MEDLINE | ID: mdl-16910371
12.
Hoarding in obsessive-compulsive disorder: clinical and genetic correlates.
J Clin Psychiatry
; 66(9): 1155-60, 2005 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-16187774
13.
Diagnostic disparity and identification of two TNNI3 gene mutations, one novel and one arising de novo, in South African patients with restrictive cardiomyopathy and focal ventricular hypertrophy.
Cardiovasc J Afr
; 26(2): 63-9, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25940119
14.
Obsessive-compulsive disorder and the promoter region polymorphism (5-HTTLPR) in the serotonin transporter gene (SLC6A4): a negative association study in the Afrikaner population.
Int J Neuropsychopharmacol
; 3(4): 327-331, 2000 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-11343612
15.
Investigating the role of dopaminergic and serotonergic candidate genes in obsessive-compulsive disorder.
Eur Neuropsychopharmacol
; 13(2): 93-8, 2003 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-12650952
16.
Corrigendum to "gender in obsessive-compulsive disorder: clinical and genetic findings" [Eur. Neuropsychopharmacol. 14 (2004) 105-113].
Eur Neuropsychopharmacol
; 14(5): 437-45, 2004 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-15468463
17.
Gender in obsessive-compulsive disorder: clinical and genetic findings.
Eur Neuropsychopharmacol
; 14(2): 105-13, 2004 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-15013025
18.
Early- versus late-onset obsessive-compulsive disorder: investigating genetic and clinical correlates.
Psychiatry Res
; 128(2): 175-82, 2004 Sep 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-15488960
19.
AKAP9 is a genetic modifier of congenital long-QT syndrome type 1.
Circ Cardiovasc Genet
; 7(5): 599-606, 2014 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25087618
20.
MT-CYB mutations in hypertrophic cardiomyopathy.
Mol Genet Genomic Med
; 1(1): 54-65, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24498601