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2p12-p13

A chromosome band present on 2p
National Institutes of Health

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Chromosome 2 Short ArmChromosomes

Papers overview

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2000
2000
Evaluation of the HOX11L1 gene as a candidate for congenital disorders of intestinal innervation
Editor—Homeobox (Hox) gene products are characterised by the presence of a highly conserved 20 amino acid region (homeodomain… 
2000
2000
Tissue-specific splicing of Omi stress-regulated endoprotease leads to an inactive protease with a modified PDZ motif.
Omi is a human serine protease whose catalytic domain is homologous to a bacterial heat shock endoprotease (HtrA), a protein… 
1996
1996
Assignment of human KH-box-containing genes by in situ hybridization: HNRNPK maps to 9q21.32-q21.33, PCBP1 to 2p12-p13, and PCBP2 to 12q13.12-q13.13, distal to FRA12A.
This report describes the localization of various human KH-box-containing genes using fluorescence in situ hybridization… 
Highly Cited
1996
Highly Cited
1996
Genetic and physical mapping at the limb-girdle muscular dystrophy locus (LGMD2B) on chromosome 2p.
The limb-girdle muscular dystrophies (LGMD) are a genetically heterogeneous group of disorders, different forms of which have… 
1996
1996
Localization of the human glucosidase I gene to chromosome 2p12-p13 by fluorescence in situ hybridization and PCR analysis of somatic cell hybrids.
This report describes the localization of the human glucosidase I gene to human chromosome 2p12-p13 by the methods of… 
1994
1994
Assignment of the human MAD and MXI1 genes to chromosomes 2p12-p13 and 10q24-q25.
MAD and MXI1, two recently described members of the basic helix-loop-helix (bHLH) gene family, encode proteins that dimerize with… 
Highly Cited
1993
Highly Cited
1993
mnd2: a new mouse model of inherited motor neuron disease.
The autosomal recessive mutation mnd2 results in early onset motor neuron disease with rapidly progressive paralysis, severe… 
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