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TNXA gene

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

Papers overview

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2018
2018
As the major glia in PNS, Schwann cells play a critical role in peripheral nerve injury repair. Finding an efficient approach to… Expand
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2009
2009
Inter-individual gene copy-number variations (CNVs) probably afford human populations the flexibility to respond to a variety of… Expand
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Review
2005
Review
2005
Two types of chimeric RCCX modules found in chromosome 6p21.3 are the chimeras CYP21P/CYP21 and TNXA/TNXB. The CYP21P-specific… Expand
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2004
2004
Detection of the CYP21 deletion in congenital adrenal hyperplasia (CAH) in the RCCX module has been previously done by Southern… Expand
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2004
2004
Arterial tortuosity syndrome (ATS) is a rare hereditary disorder with variable clinical presentation including tortuosity and… Expand
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2000
2000
  • Z. Yang, C. Y. Yu
  • Experimental and Clinical Immunogenetics
  • 2000
  • Corpus ID: 45164668
The MHC complement gene cluster (MCGC) in most people contains thirteen structural genes, pseudogenes and gene segments. Novel… Expand
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Highly Cited
1999
Highly Cited
1999
The frequent variations of human complement component C4 gene size and gene numbers, plus the extensive polymorphism of the… Expand
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1999
1999
The central class III region of the human major histocompatibility complex contains highly polymorphic genes that are associated… Expand
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1999
1999
The RCCX module of the human MHC class III region is comprised of four genes arranged in tandem: RP, complement C4, steroid 21… Expand
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Review
1998
Review
1998
  • 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… Expand
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