Z A M H Zabidi-Hussin
Overview
Explore the profile of Z A M H Zabidi-Hussin including associated specialties, affiliations and a list of published articles.
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14
Citations
116
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Recent Articles
1.
Ismail N, Rani A, Nik Abdul Malik N, Boon Hock C, Mohd Azlan S, Razak S, et al.
J Mol Diagn
. 2017 Jan;
19(2):265-276.
PMID: 28087349
Tuberous sclerosis complex (TSC) is an autosomal dominant neurocutaneous disorder characterized by tumor growth in multiple organs and caused by mutations in either TSC1 or TSC2 genes. Because of their...
2.
Mohseni J, Al-Najjar B, Wahab H, Zabidi-Hussin Z, Sasongko T
J Hum Genet
. 2016 Jun;
61(9):823-30.
PMID: 27251006
Several histone deacetylase inhibitors (HDACis) are known to increase Survival Motor Neuron 2 (SMN2) expression for the therapy of spinal muscular atrophy (SMA). We aimed to compare the effects of...
3.
Sasongko T, Ismail N, Nik Abdul Malik N, Zabidi-Hussin Z
Orphanet J Rare Dis
. 2015 Aug;
10:95.
PMID: 26259610
Background: Rapamycin has gained significant attention for its potential activity in reducing the size of TSC-associated tumors, thus providing alternative to surgery. This study aimed at determining the efficacy of...
4.
Sasongko T, Ismail N, Nik Mohd Ariff N, Zabidi-Hussin Z
Jpn J Clin Oncol
. 2014 Oct;
44(11):1130.
PMID: 25320338
No abstract available.
5.
Ismail N, Nik Abdul Malik N, Mohseni J, Rani A, Hayati F, Salmi A, et al.
Jpn J Clin Oncol
. 2014 Apr;
44(5):506-11.
PMID: 24683199
Tuberous sclerosis complex is an autosomal dominant neurocutaneous disorder affecting multiple organs. Tuberous sclerosis complex is caused by mutation in either one of the two disease-causing genes, TSC1 or TSC2,...
6.
Mohseni J, Zabidi-Hussin Z, Sasongko T
Genet Mol Biol
. 2013 Oct;
36(3):299-307.
PMID: 24130434
Histone acetylation plays an important role in regulation of transcription in eukaryotic cells by promoting a more relaxed chromatin structure necessary for transcriptional activation. Histone deacetylases (HDACs) remove acetyl groups...
7.
Rani A, Sasongko T, Sulong S, Bunyan D, Salmi A, Zilfalil B, et al.
J Neurogenet
. 2013 Feb;
27(1-2):11-5.
PMID: 23438214
We undertook the clinical feature examination and dystrophin analysis using multiplex ligation-dependent probe amplification (MLPA) and direct DNA sequencing of selected exons in a cohort of 35 Malaysian Duchenne/Becker muscular...
8.
9.
Marini M, Sasongko T, Watihayati M, Atif A, Hayati F, Zabidi-Hussin Z, et al.
Indian J Med Res
. 2012 Mar;
135:31-5.
PMID: 22382180
Background & Objectives: Genetic diagnosis of spinal muscular atrophy (SMA) is complicated by the presence of SMN2 gene as majority of SMA patients show absence or deletion of SMN1 gene....
10.
Rani A, Malueka R, Sasongko T, Awano H, Lee T, Yagi M, et al.
Mol Genet Metab
. 2011 Apr;
103(3):303-4.
PMID: 21514860
In Duchenne muscular dystrophy (DMD), identification of one nonsense mutation in the DMD gene has been considered an endpoint of genetic diagnosis. Here, we identified two closely spaced nonsense mutations...