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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

Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
Saving mothers and newborns in communities: strengthening community midwives to provide high quality essential newborn and maternal care in Baluchistan, Pakistan in a financially sustainable manner
BackgroundTo address it's persistently high maternal mortality rate of 276/100,000 live births, the government of Pakistan… 
Highly Cited
2009
Highly Cited
2009
Adsorption of As(V) on surfactant-modified natural zeolites.
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… 
2008
2008
Cognitive and Neuromuscular Assessment in Geriatric Patients with Thyroid Dysfunction
The aim of this study is to evaluate objectively, the functional changes in the nervous system, central changes (cognitive… 
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
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
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
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… 
1987
1987
A virtual statistical mechanical neural computer.
Abstract : The study applies recently developed statistical algorithms and an innovative large system scaling technique to the… 
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