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SGCZ gene

Known as: sarcoglycan zeta, ZSG1, SGCZ 
 
National Institutes of Health

Papers overview

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2017
2017
A novel relationship for schizophrenia, bipolar and major depressive disorder Part 5: a hint from chromosome 5 high density association screen.
Familial clustering of schizophrenia (SCZ), bipolar disorder (BPD), and major depressive disorder (MDD) was systematically… Expand
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2017
2017
The Value of MiR-383, an Intronic MiRNA, as a Diagnostic and Prognostic Biomarker in Intestinal-Type Gastric Cancer
MicroRNAs, a class of gene expression regulatory non-coding RNAs, participate in the pathogenic mechanisms of gastric cancer… Expand
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2016
2016
Shutdown of HIV-1 Transcription in T Cells by Nullbasic, a Mutant Tat Protein
UNLABELLED Nullbasic is a derivative of the HIV-1 transactivator of transcription (Tat) protein that strongly inhibits HIV-1… Expand
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2014
2014
SGCZ mutations are unlikely to be associated with myoclonus dystonia
BACKGROUND Myoclonus dystonia syndrome (MDS) is a hyperkinetic movement disorder caused, in a proportion of cases, by mutations… Expand
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Highly Cited
2012
Highly Cited
2012
Transactivation of microRNA-383 by steroidogenic factor-1 promotes estradiol release from mouse ovarian granulosa cells by targeting RBMS1.
Our previous studies have shown that microRNA-383 (miR-383) is one of the most down-regulated miRNA in TGF-β1-treated mouse… Expand
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2012
2012
Copy number variations associated with obesity related traits in African Americans: a joint analysis between GENOA and HyperGEN
Obesity is a highly heritable trait and a growing public health problem. African Americans are a genetically diverse, yet… Expand
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2008
2008
Detection of exonic copy-number changes using a highly efficient oligonucleotide-based comparative genomic hybridization-array method.
Genomic copy-number variations (CNVs) involving large DNA segments are known to cause many genetic disorders. Depending on the… Expand
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2008
2008
A novel locus for generalized epilepsy with febrile seizures plus in French families.
BACKGROUND Generalized epilepsy with febrile seizures plus (GEFS(+)) is a familial autosomal dominant entity characterized by the… Expand
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2008
2008
Candidate-gene testing for orphan limb-girdle muscular dystrophies.
The term limb-girdle muscular dystrophies (LGMD) identify about two dozens of distinct genetic disorders. Additional genes must… Expand
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Review
1997
Review
1997
[Adhalin(alpha-sarcoglycan) gene mutations in patients with malignant limb-girdle muscular dystrophy (MLGMD) (Miyoshi)].
Malignant limb-girdle muscular dystrophy (MLGMD) (Miyoshi) is considered to be roughly the same as SCARMD (Ben Hamida) in its… Expand
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