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19q13.4

A chromosome band present on 19q
National Institutes of Health

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15 relations
19qCNOT3 wt AlleleChromosomesFPR1 wt Allele

Papers overview

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2006
2006
Mesenchymal hamartoma of the liver with an interstitial deletion involving chromosome band 19q13.4: a theory as to pathogenesis?
Mesenchymal hamartoma of the liver is the third most common liver tumor of infancy. The lesion is primarily mesenchymal in origin… 
2004
2004
Mapping of a translocation breakpoint in a Peutz–Jeghers hamartoma to the putative PJS locus at 19q13.4 and mutation analysis of candidate genes in polyp and STK11‐negative PJS cases
Germ‐line mutations in the serine‐threonine kinase gene STK11 (LKB1) cause Peutz–Jeghers syndrome (PJS), a rare autosomal… 
Highly Cited
2004
Highly Cited
2004
SNP haplotypes and allele frequencies show evidence for disruptive and balancing selection in the human leukocyte receptor complex
The human leukocyte receptor complex (LRC) of Chromosome 19q13.4 encodes polymorphic and highly homologous genes that are… 
2004
2004
Characterization and chondrocyte differentiation stage-specific expression of KRAB zinc-finger protein gene ZNF470.
2003
2003
Distribution of LILRA3 (ILT6/LIR4) deletion in psoriatic patients and healthy controls.
2001
2001
Delineation of a 150-kb breakpoint cluster in benign thyroid tumors with 19q13.4 aberrations
Structural rearrangements involving the long arm of chromosome 19 characterize a cytogenetic subgroup of benign thyroid tumors… 
2001
2001
Conserved organization of the ILT/LIR gene family within the polymorphic human leukocyte receptor complex
Abstract. The human leukocyte receptor complex (LRC) at Chromosome 19q13.4 encodes Ig superfamily proteins which regulate the… 
1999
1999
NILR‐1, a novel immunoglobulin‐like receptor expressed by neutrophilic granulocytes, is encoded by a leukocyte receptor gene complex on rat chromosome 1
Several receptors expressed by subsets of leukocytes and with sequence homology to the killer cell inhibitory receptors have… 
1995
1995
FISH analyses of a newly established thyroid tumor cell line showing a t(1;19)(p35 or p36.1;q13) reveal that the breakpoint lies between 19q13.3-13.4 and 19q13.4.
Translocations involving the long arm of human chromosome 19 are specific chromosomal alterations found in a subset of benign… 
1994
1994
Assignment of the human lens fiber cell MP19 gene (LIM2) to chromosome 19q13.4, and adjacent to ETFB
The LIM2 gene may play a major role in lens fiber cell structure or communication, and thus cataractogenesis. A human cDNA… 
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