Detalhe da pesquisa
1.
Rapamycin and rapalogs for tuberous sclerosis complex.
Cochrane Database Syst Rev
; 7: CD011272, 2023 07 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37432030
2.
Angiotensin-converting enzyme (ACE) inhibitors for proteinuria and microalbuminuria in people with sickle cell disease.
Cochrane Database Syst Rev
; 12: CD009191, 2021 12 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-34932828
3.
The role of mTOR signalling pathway in hypoxia-induced cognitive impairment.
Int J Neurosci
; 131(5): 482-488, 2021 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-32202188
4.
In Silico Analyses and Cytotoxicity Study of Asiaticoside and Asiatic Acid from Malaysian Plant as Potential mTOR Inhibitors.
Molecules
; 25(17)2020 Sep 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32887218
5.
Placebo Controlled Trials: Interests of Subjects versus Interests of Drug Regulators.
Malays J Med Sci
; 24(4): 1-4, 2017 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-28951684
6.
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
7.
Informed Consent Template and Guidelines on the Ethical Practice in Human Genetics and Human Genomic Research; Initiatives of the Universiti Sains Malaysia.
Malays J Med Sci
; 22(6): 47-53, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-28223885
8.
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
9.
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
10.
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
11.
Gene and schizophrenia in the pregenome and postgenome-wide association studies era: a bibliometric analysis and network visualization.
Psychiatr Genet
; 33(2): 37-49, 2023 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36825838
12.
Two-years antibody responses following SARS-CoV-2 infection in humans: A study protocol.
PLoS One
; 17(8): e0272690, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35972930
13.
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
14.
Deletion analysis of SMN1 exon 7 alone may be necessary and sufficient for the diagnosis of spinal muscular atrophy.
J Neurogenet
; 25(1-2): 15-6, 2011 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-21338334
15.
Nomenclature Confusion in Deletion Mutations Involving Repetitive Nucleotides: A Lesson from HBB Gene Codon 35 (-C) vs. Codon 36 (-C).
Hemoglobin
; 39(6): 452-3, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26291969
16.
Macrodactyly and poliosis in tuberous sclerosis complex.
Jpn J Clin Oncol
; 44(11): 1130, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-25320338
17.
SMN2 and NAIP gene dosages in Vietnamese patients with spinal muscular atrophy.
Pediatr Int
; 50(3): 346-51, 2008 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-18533950
18.
Antiphospholipid antibodies in epilepsy: A systematic review and meta-analysis.
Autoimmun Rev
; 17(8): 755-767, 2018 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-29885542
19.
A novel mutation at the N-terminal of SMN Tudor domain inhibits its interaction with target proteins.
J Neurol
; 254(5): 624-30, 2007 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-17415510
20.
Presence of Anticardiolipin Antibodies in Patients with Dementia: A Systematic Review and Meta-Analysis.
Front Aging Neurosci
; 9: 250, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28824414