FAQ

SMN2 wt Allele

Known as: Survival of Motor Neuron 2, Centromeric wt Allele, BCD541, Tudor Domain Containing 16B Gene 
Human SMN2 wild-type allele is located in the vicinity of 5q13.2 and is approximately 29 kb in length. This allele, which encodes survival motor… (More)
National Institutes of Health

Topic mentions per year

Topic mentions per year

1987-2014
012319872014

Related topics

Related topics

3 relations
RNA SplicingSMN2 geneprotein protein interaction

Related mentions per year

Related mentions per year

1954-2018
1960198020002020
SMN2 wt Allele
RNA Splicing
protein protein interaction
SMN2 gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2009
2009
Adsorption of As(V) on surfactant-modified natural zeolites.
Natural mordenite (NM), natural clinoptilolite (NC), HDTMA-modified natural mordenite (SMNM) and HDTMA-modified natural… (More)
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2009
2009
Superparamagnetic magnetite nanocrystal clusters: a sensitive tool for MR cellular imaging.
Silica coated, PEI and citric acid hybrid superparamagnetic magnetite nanocrystal clusters (SMNC) were synthesized using either a… (More)
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2009
2009
Diagnostic efficacy of midnight cortisol and midnight ACTH in the diagnosis and localisation of Cushing’s syndrome
Classical tests for diagnosis of Cushing’s syndrome (CS) like urine free cortisol and dexamethasone suppression tests have… (More)
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1999
1999
Promoter analysis of the human centromeric and telomeric survival motor neuron genes (SMNC and SMNT).
Proximal spinal muscular atrophy (SMA) is caused by mutations in the telomeric (SMNT), but not centromeric (SMNC), survival motor… (More)
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1998
1998
Correlation of SMNt and SMNc gene copy number with age of onset and survival in spinal muscular atrophy
Childhood-onset autosomal recessive spinal muscular atrophy (SMA) is associated with absence of the telomeric survival motor… (More)
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1998
1998
Association between centromeric deletions of the SMN gene and sporadic adult-onset lower motor neuron disease.
The telomeric copy (t) of the survival motor neuron (SMN) gene is homozygously deleted in more than 90% of patients with… (More)
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Highly Cited
1997
Highly Cited
1997
Identification of proximal spinal muscular atrophy carriers and patients by analysis of SMNT and SMNC gene copy number.
The survival motor neuron (SMN) transcript is encoded by two genes, SMNT and SMNC. The autosomal recessive proximal spinal… (More)
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1996
1996
An 11 base pair duplication in exon 6 of the SMN gene produces a type I spinal muscular atrophy (SMA) phenotype: further evidence for SMN as the primary SMA-determining gene.
The gene for autosomal recessive spinal muscular atrophy (SMA) has been mapped to 5q12 in a region that contains repeated markers… (More)
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1996
1996
In vitro induction of anti-type 2 T cells by glycyrrhizin.
Glycyrrhizin (GR), an active component of licorice roots, has been previously shown to induce the generation of anti-type 2 T… (More)
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1989
1989
Analysis of the decreased NK (natural killer) activity in lung cancer patients, using whole blood versus separated mononuclear cells.
The aim of this study was to analyze whether a whole blood assay would give a more correct measure of NK activity than assays… (More)
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