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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.
2018
2018
lncRNA TNXA-PS1 Modulates Schwann Cells by Functioning As a Competing Endogenous RNA Following Nerve Injury
As the major glia in PNS, Schwann cells play a critical role in peripheral nerve injury repair. Finding an efficient approach to… 
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2009
2009
Great genotypic and phenotypic diversities associated with copy-number variations of complement C4 and RP-C4-CYP21-TNX (RCCX) modules: a comparison of Asian-Indian and European American populations.
Inter-individual gene copy-number variations (CNVs) probably afford human populations the flexibility to respond to a variety of… 
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Review
2005
Review
2005
Chimeric CYP21P/CYP21 and TNXA/TNXB genes in the RCCX module.
Two types of chimeric RCCX modules found in chromosome 6p21.3 are the chimeras CYP21P/CYP21 and TNXA/TNXB. The CYP21P-specific… 
2004
2004
PCR-based detection of the CYP21 deletion and TNXA/TNXB hybrid in the RCCX module.
Detection of the CYP21 deletion in congenital adrenal hyperplasia (CAH) in the RCCX module has been previously done by Southern… 
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
2001
Review
2001
Genetic, structural and functional diversities of human complement components C4A and C4B and their mouse homologues, Slp and C4.
The complement protein C4 is a non-enzymatic component of the C3 and C5 convertases and thus essential for the propagation of the… 
Highly Cited
1999
Highly Cited
1999
Modular Variations of the Human Major Histocompatibility Complex Class III Genes for Serine/Threonine Kinase RP, Complement Component C4, Steroid 21-Hydroxylase CYP21, and Tenascin TNX (the RCCX…
The frequent variations of human complement component C4 gene size and gene numbers, plus the extensive polymorphism of the… 
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1999
1999
Homozygous deletion of the CYP21A-TNXA-RP2-C4B gene region conferring C4B deficiency associated with recurrent respiratory infections.
The central class III region of the human major histocompatibility complex contains highly polymorphic genes that are associated… 
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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Review
1998
Review
1998
Molecular Genetics of the Human MHC Complement Gene Cluster
  • C. Y. Yu
  • Experimental and Clinical Immunogenetics
  • 1998
  • Corpus ID: 25061446
The human major histocompatibility complex (MHC) complement gene cluster (MCGC) is a highly variable region that is characterized… 
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