Detalhe da pesquisa
1.
Transcript, methylation and molecular docking analyses of the effects of HDAC inhibitors, SAHA and Dacinostat, on SMN2 expression in fibroblasts of SMA patients.
J Hum Genet
; 61(9): 823-30, 2016 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-27251006
2.
Two novel gross deletions of TSC2 in Malaysian patients with tuberous sclerosis complex and TSC2/PKD1 contiguous deletion syndrome.
Jpn J Clin Oncol
; 44(5): 506-11, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24683199
3.
Mutation spectrum of dystrophin gene in malaysian patients with Duchenne/Becker muscular dystrophy.
J Neurogenet
; 27(1-2): 11-5, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-23438214
4.
Histone deacetylase inhibitors as potential treatment for spinal muscular atrophy.
Genet Mol Biol
; 36(3): 299-307, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-24130434
5.
Allele-specific PCR for a cost-effective & time-efficient diagnostic screening of spinal muscular atrophy.
Indian J Med Res
; 135: 31-5, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22382180
6.
Two closely spaced nonsense mutations in the DMD gene in a Malaysian family.
Mol Genet Metab
; 103(3): 303-4, 2011 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-21514860
7.
Biochemical profiling to predict disease severity in metachromatic leukodystrophy.
Mol Genet Metab
; 99(2): 142-8, 2010 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-19815439
8.
Macrodactyly and poliosis in tuberous sclerosis complex.
Jpn J Clin Oncol
; 44(11): 1130, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-25320338
9.
Combination of Multiple Ligation-Dependent Probe Amplification and Illumina MiSeq Amplicon Sequencing for TSC1/TSC2 Gene Analyses in Patients with Tuberous Sclerosis Complex.
J Mol Diagn
; 19(2): 265-276, 2017 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-28087349
10.
Rapamycin and its analogues (rapalogs) for Tuberous Sclerosis Complex-associated tumors: a systematic review on non-randomized studies using meta-analysis.
Orphanet J Rare Dis
; 10: 95, 2015 Aug 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-26259610
11.
Challenges in clinical research in Malaysia.
Med J Malaysia
; 62(4): 275-7, 2007 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-18551927
12.
Screening of the LIX1 gene in Japanese and Malaysian patients with SMA and/or SMA-like disorder.
Brain Dev
; 32(5): 385-9, 2010 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-19664890
13.
Combination of SMN2 copy number and NAIP deletion predicts disease severity in spinal muscular atrophy.
Brain Dev
; 31(1): 42-5, 2009 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-18842367
14.
Does nondisclosure of genetic paternity status constitute a breach of ethics?: Commentary on "The dilemma of revealing sensitive information on paternity status in Arabian social and cultural contexts" by Abdallah A. Adlan and Henk A. M. J. ten Have.
J Bioeth Inq
; 9(4): 413-4, 2012 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-23188398