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14q11.2

A chromosome band present on 14q
National Institutes of Health

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21 relations
AJUBA wt AlleleCCNB1IP1 wt AlleleCEBPE wt AlleleCHD8 wt Allele

Papers overview

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Review
2018
Review
2018
Constitutional Partial Proximal Trisomy 14q11.2 to 14q21: Two New Moroccan Cases and Review of the Literature
2018
2018
t(X;14)(q28;q11.2) TRA-TRD/MTCP1
T-cell prolymphocytic leukemia (T-PLL) is a rare and aggressive post-thymic lymphoid neoplasm characterized by recurrent… 
2011
2011
Erratum to: Population and Computational Analysis of the MGEA6 P521A Variation as a Risk Factor for Familial Idiopathic Basal Ganglia Calcification (Fahr’s Disease)
2007
2007
BCL 2 L 2 is a probable target for novel 14 q 11 . 2 amplification detected in a non-small cell lung cancer cell line
Department of Molecular Cytogenetics, Medical Research Institute and School of Biomedical Science, Department of Integrated… 
2007
2007
Genome Wide-DNA Profiling of HIV-Related Non-Hodgkin Lymphomas: Implications for Disease Pathogenesis and Histogenesis.
Non-Hodgkin’s lymphomas (NHL) represent a frequent complication of HIV infection and a major source of morbidity and mortality… 
2006
2006
Chromosomal imbalances and their target genes in gastrointestinal stromal tumors
Gastrointestinal stromal tumor (GIST) is a mesenchymal sarcoma of the gastrointestinal tract. The tumors characteristically… 
1999
1999
The 5' flanking region of the human granzyme H gene directs expression to T/natural killer cell progenitors and lymphokine-activated killer cells in transgenic mice.
Human granzyme H is a neutral serine protease that is expressed predominantly in the lymphokine-activated killer (LAK)/natural… 
1999
1999
[An analysis of the linkage of hypertrophic cardiomyopathy and the delta locus of the T-cell receptor (TCRD) chain in the family of P].
AIM To estimate probability of location of the gene determining family hypertrophic cardiomyopathy (HCMP) in family P. on the… 
1998
1998
Identification and Characterization of a Membrane Protein ( y 1 L Amino Acid Transporter-1 ) That Associates with 4 F 2 hc to Encode the Amino Acid Transport Activity y 1
We have identified a new human cDNA (yL amino acid transporter-1 (yLAT-1)) that induces system yL transport activity with 4F2hc… 
1994
1994
Mapping of the first preferentially expressed cDNA in human fetal cochlea to human 14q11.2-12 and to a region of homologous synteny on mouse chromosome 12
We have isolated a cDNA, Coch-5B2 (D14S564E) from a human fetal cochlear cDNA library by subtractive hybridization and…