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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… 
National Institutes of Health

Related topics

Related topics

3 relations
RNA SplicingSMN2 geneprotein protein interaction

Papers overview

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Highly Cited
2009
Highly Cited
2009
Adsorption of As(V) on surfactant-modified natural zeolites.
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… 
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… 
Highly Cited
1999
Highly Cited
1999
Promoter analysis of the human centromeric and telomeric survival motor neuron genes (SMNC and SMNT).
1999
1999
Significance of endogenous heat shock protein in adjuvant arthritis.
OBJECTIVE To investigate the role of endogenous heat shock protein (HSP) (rat 60 kDa HSP, rHSP 60) in adjuvant arthritis (AA… 
Highly Cited
1998
Highly Cited
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… 
Highly Cited
1998
Highly Cited
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… 
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… 
Highly Cited
1996
Highly Cited
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… 
1993
1993
Induction of Acute Arthritis in Mice by Peptidoglycan Derived from Gram‐Positive Bacteria and Its Possible Role in Cytokine Production
The activities of a water‐soluble peptidoglycan fragment derived from Staphylococcus epidermidis (SEPS) were examined as to their… 
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