FAQ

Xq22-24

A chromosome band present on Xq
National Institutes of Health

Topic mentions per year

Topic mentions per year

1994-2006
0119942006

Related topics

Related topics

1 relation
Chromosomes

Related mentions per year

Related mentions per year

1936-2018
19401960198020002020
Xq22-24
Chromosomes

Papers overview

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2006
2006
Characterization of the MCT-1 pseudogene: identification and implication of its location in a highly amplified region of chromosome 20.
The MCT-1 oncogene was initially identified as an amplified gene on chromosome Xq22-24 in a T-cell lymphoma. MCT-1 is over… (More)
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2003
2003
Expression of the candidate MCT-1 oncogene in B- and T-cell lymphoid malignancies.
Our laboratory has recently discovered a novel candidate oncogene, MCT-1, amplified in human T-cell lymphoma and mapped to… (More)
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Review
2003
Review
2003
MLL/SEPTIN6 chimeric transcript from inv ins(X;11)(q24;q23q13) in acute monocytic leukemia: report of a case and review of the literature.
Rearrangements of the MLL gene on chromosome 11, band q23, are one of the most common genetic changes in acute leukemia… (More)
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2002
2002
SEPTIN6, a human homologue to mouse Septin6, is fused to MLL in infant acute myeloid leukemia with complex chromosomal abnormalities involving 11q23 and Xq24.
t(X;11) is a recurrent translocation in pediatric acute myeloid leukemia (AML). We showed that the MLL gene on 11q23 was fused to… (More)
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2001
2001
Expression and stabilization of the MCT-1 protein by DNA damaging agents
The contribution of oncogene amplification and/or overexpression to T-cell lymphoid neoplasms has only of late been established… (More)
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2000
2000
Identification of a highly polymorphic microsatellite within the bovine ectodysplasin A (ED1) gene on BTA Xq22-24.
 
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1998
1998
A novel candidate oncogene, MCT-1, is involved in cell cycle progression.
Using the arbitrarily primed-PCR (AP-PCR) assay to detect genetic abnormalities that occur in a panel of lymphoid cell lines, we… (More)
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Review
1997
Review
1997
The clinical spectrum of type IV collagen mutations.
Clinical manifestations of type IV collagen mutations can vary from the severe, clinically and genetically heterogeneous renal… (More)
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1994
1994
Effect of telomeres on the interphase location of adjacent regions of the human X chromosome.
Chromosomes occupy specific nonrandom domains in the interphase nucleus of eukaryotic cells. We have used a Chinese hamster-human… (More)
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