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Alleles, X-Linked

Known as: X-Linked Alleles, X-Linked Allele, Alleles, X Linked 
National Institutes of Health

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Genes, X-Linked

Papers overview

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2015
2015
Explorer The Asp 84 Glu variant of the melanocortin 1 receptor ( MC 1 R ) is associated with melanoma
Melanocyte stimulating hormone (MSH) plays an important role in determining the cutaneous response to ultraviolet radiation and… 
2009
2009
Protective role of the HLA–A*02 allele in Portuguese patients with multiple sclerosis
Background Multiple sclerosis (MS) is associated with human leukocyte antigen (HLA) HLA–DRB1*15. Recent evidence that CD8 T cells… 
Review
2008
Review
2008
CcrB typing tool: an online resource for staphylococci ccrB sequence typing.
Sir, In 2006, we published a manuscript in this journal describing the allelic variation in the ccrAB locus in a representative… 
2007
2007
Identification of genetic variations of exon 2 of BoLA‐DQB gene in five Chinese yellow cattle breeds
One hundred and eighty animals from five Chinese yellow cattle breeds were used to identify genetic variations in the exon 2 of… 
2003
2003
Association between pepsinogen C gene polymorphism and genetic predisposition to gastric cancer.
AIM To identify a molecular marker for gastric cancer, and to investigate the relationship between the polymorphism of pepsinogen… 
2003
2003
The HRAS1 variable number of tandem repeats and risk of breast cancer.
Rare alleles at the HRAS1 variable number of tandem repeats (VNTRs) locus have been implicated in breast cancer risk. We assessed… 
1999
1999
HRAS1 rare minisatellite alleles and breast cancer in Australian women under age forty years.
BACKGROUND A recent meta-analysis of 23 studies supported the empirically derived hypothesis that women who lack one of the four… 
1998
1998
Polymorphisms of the apolipoprotein B 3' variable number of tandem repeats region associated with coronary artery disease in Taiwanese.
We studied the allelic frequency of the variable number of tandem repeats region 3' of the apolipoprotein B gene (apoB 3' VNTR… 
1991
1991
Novel SOS phenotypes caused by second-site mutations in the recA430 gene of Escherichia coli.
1986
1986
Analysis of multiple restriction fragment length polymorphisms of the gene for the human complement receptor type I. Duplication of genomic sequences occurs in association with a high molecular mass…
Human CR1 exhibits an unusual form of polymorphism in which allotypic variants differ in the molecular weight of their respective… 
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