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TNXA gene

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

Related topics

Related topics

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TNXB gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
The prevalence of chimeric TNXA/TNXB gene and clinical symptoms of Ehlers-Danlos syndrome with 21-hydroxylase deficiency.
PURPOSE Defects in both CYP21A2 and TNXB genes can cause congenital adrenal hyperplasia combined with hypermobility type Ehlers… 
2018
2018
Integrated Proteomics and Lipidomics Investigation of the Mechanism Underlying the Neuroprotective Effect of N-benzylhexadecanamide
Macamides are very important secondary metabolites produced by Lepidium meyenii Walp, which possess multiple bioactivities… 
2014
2014
Memory-related gene expression profile of the male rat hippocampus induced by teeth extraction and occlusal support recovery.
2014
2014
Long noncoding RNA expression signatures of bladder cancer revealed by microarray
Dysregulation of long noncoding RNAs (lncRNAs) has been regarded as a primary feature of several human cancers. However, the… 
2009
2009
Genetic deficiency of complement isoforms C4A or C4B predicts improved survival of metastatic renal cell carcinoma.
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… 
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… 
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