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TNXA gene

Known as: TNXA, HXBL, XA 
National Institutes of Health

Related topics

Related topics

1 relation
TNXB gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Measurement of serum tenascin-X in patients with congenital adrenal hyperplasia at risk for Ehlers–Danlos contiguous gene deletion syndrome CAH-X
Approximately 10% of patients with congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency carry a mutation that… 
2014
2014
Memory-related gene expression profile of the male rat hippocampus induced by teeth extraction and occlusal support recovery.
2011
2011
Analysis of the CYP21A2 gene with intergenic recombination and multiple gene deletions in the RCCX module.
The most frequent bimodular RCCX module of the RP1-C4A-CYP21A1P-TNXA-RP2-C4B-CYP21A2-TNXB gene sequence is located on chromosome… 
2008
2008
Low frequency of the CYP21A2 deletion in ethnic Chinese (Taiwanese) patients with 21-hydroxylase deficiency.
Review
2005
Review
2005
Diversity of the CYP21P-like gene in CYP21 deficiency.
More than 90% of cases of congenital adrenal hyperplasia (CAH) are caused by mutations of the CYP21 gene. The occurrence of… 
2004
2004
Exclusion of candidate genes in a family with arterial tortuosity syndrome
Arterial tortuosity syndrome (ATS) is a rare hereditary disorder with variable clinical presentation including tortuosity and… 
Review
2003
Review
2003
Mapping of a de novo unequal crossover causing a deletion of the steroid 21-hydroxylase (CYP21A2) gene and a non-functional hybrid tenascin-X (TNXB) gene
In the human genome, the major histocompatibility complex class III region on chromosome 6p21.3 stands out as an area of… 
2000
2000
Organizations and Gene Duplications of the Human and Mouse MHC Complement Gene Clusters1
The MHC complement gene cluster (MCGC) in most people contains thirteen structural genes, pseudogenes and gene segments. Novel… 
1999
1999
An Unequal Crossover between the RCCX Modules of the Human MHC Leading to the Presence of a CYP21B Gene and a Tenascin TNXB/TNXA-RP2 Recombinant between C4A and C4B Genes in a Patient with Juvenile…
The RCCX module of the human MHC class III region is comprised of four genes arranged in tandem: RP, complement C4, steroid 21… 
1999
1999
Homozygous deletion of the CYP21A-TNXA-RP2-C4B gene region conferring C4B deficiency associated with recurrent respiratory infections.
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