Skip to search formSkip to main contentSkip to account menu

SLC26A2 gene

Known as: SLC26A2, SOLUTE CARRIER FAMILY 26 (SULFATE TRANSPORTER), MEMBER 2, solute carrier family 26 member 2 
National Institutes of Health

Related topics

Related topics

1 relation

Narrower (1)

Atelosteogenesis type 2

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2010
2010
New intermediate phenotype between MED and DD caused by compound heterozygous mutations in the DTDST gene
DTDST mutations cause a spectrum of diastrophic dysplasia disorders characterized by defects of proteoglycans sulfation… 
2010
2010
Imaging the spectrum of DTDST gene mutations
Poster: "ECR 2011 / C-0026 / Imaging the spectrum of DTDST gene mutations" by: "S. F. Miller; Memphis, TN/US" 
2009
2009
Diastrofik Displazi: Vaka Sunumu
Diastrophic dysplasia (DTD) is a rare syndrome which is characterized by disproportionate short stature, normal-sized skull… 
2009
2009
DIASTROPHIC DYSPLASIA: CASE REPORT
Diastrophic dysplasia (DTD) is a rare syndrome which is characterized by disproportionate short stature, normal-sized skull… 
2005
2005
Suppressed transcription of genes for sulfate transporter, DTDST, as a major mechanism for induction of a carbohydrate tumor marker sialyl Lewisx in colon cancers
2002
2002
DTDST mutations are not a frequent cause of idiopathic talipes equinovarus (club foot)
Idiopathic talipes equinovarus (ITEV) or isolated club foot deformity is a common birth defect having an average birth prevalence… 
Review
2001
Review
2001
Molecular Mechanisms in Renal and Intestinal Sulfate (Re)Absorption
Inorganic sulfate is an essential cofactor for sulfate conjugation reactions that are responsible not only for the detoxification… 
2000
2000
Homologous mutations in two diverse sulphate transporters have similar effects
Review
1998
Review
1998
Atelosteogenesis type 2.
Atelosteogenesis type 2 (AO2) (MIM 256050) is a neonatally lethal chondrodysplasia characterised by severe limb shortening and… 
1996
1996
Phenotypic features of dentition in diastrophic dysplasia.
Diastrophic dysplasia (DTD) is a well-characterized, recessively inherited osteochondrodysplasia. The gene, DTDST, in which… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)