Mapping chromosome band 11q23 in human acute leukemia with biotinylated probes: identification of 11q23 translocation breakpoints with a yeast artificial chromosome.
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Molecular characterization of a human DNA kinaseAcute mixed-lineage leukemia t(4;11)(q21;q23) generates an MLL-AF4 fusion productCloning of ELL, a gene that fuses to MLL in a t(11;19)(q23;p13.1) in acute myeloid leukemiaIdentification of Nck family genes, chromosomal localization, expression, and signaling specificityThe t(10;11)(p13;q14) in the U937 cell line results in the fusion of the AF10 gene and CALM, encoding a new member of the AP-3 clathrin assembly protein familyA novel interleukin-12 p40-related protein induced by latent Epstein-Barr virus infection in B lymphocytesTAL2, a helix-loop-helix gene activated by the (7;9)(q34;q32) translocation in human T-cell leukemiaIdentification of a gene, MLL, that spans the breakpoint in 11q23 translocations associated with human leukemiasExpression, regulation, and chromosomal localization of the Max geneCytogenetic and molecular delineation of the smallest commonly deleted region of chromosome 5 in malignant myeloid diseasesIsolation of the human peroxisomal acyl-CoA oxidase gene: organization, promoter analysis, and chromosomal localizationConstruction of a 2.8-megabase yeast artificial chromosome contig and cloning of the human methylthioadenosine phosphorylase gene from the tumor suppressor region on 9p21HEN1 and HEN2: a subgroup of basic helix-loop-helix genes that are coexpressed in a human neuroblastomaRearrangements of the retinoic acid receptor alpha and promyelocytic leukemia zinc finger genes resulting from t(11;17)(q23;q21) in a patient with acute promyelocytic leukemiaA yeast artificial chromosome-based map of the region of chromosome 20 containing the diabetes-susceptibility gene, MODY1, and a myeloid leukemia related geneThe hybrid PAX3-FKHR fusion protein of alveolar rhabdomyosarcoma transforms fibroblasts in cultureA DNA damage and stress inducible G protein-coupled receptor blocks cells in G2/MProstate stem cell antigen: a cell surface marker overexpressed in prostate cancerAmplification and overexpression of peroxisome proliferator-activated receptor binding protein (PBP/PPARBP) gene in breast cancerChromosome localization and RFLP analysis of PDC-E2: the major autoantigen of primary biliary cirrhosisStructure of AF3p21, a new member of mixed lineage leukemia (MLL) fusion partner proteins-implication for MLL-induced leukemogenesis.GPHN, a novel partner gene fused to MLL in a leukemia with t(11;14)(q23;q24).Identification and analysis of the gene encoding human PC2, a prohormone convertase expressed in neuroendocrine tissues.Isolation of a yeast artificial chromosome spanning the 8;21 translocation breakpoint t(8;21)(q22;q22.3) in acute myelogenous leukemia.Fluorescence in situ hybridization: molecular probes for diagnosis of pediatric neoplastic diseases.The truncation that generated the v-cbl oncogene reveals an ability for nuclear transport, DNA binding and acute transformation.Molecular rearrangements of the MLL gene are present in most cases of infant acute myeloid leukemia and are strongly correlated with monocytic or myelomonocytic phenotypes.Increased genetic instability of the common fragile site at 3p14 after integration of exogenous DNA.Detection of deletions and cryptic translocations in Miller-Dieker syndrome by in situ hybridization.Molecular biology in medicine.Acute leukemias with the t(4;11)(q21;q23).Identification of the gene associated with the recurring chromosomal translocations t(3;14)(q27;q32) and t(3;22)(q27;q11) in B-cell lymphomasAnalysis of the murine All-1 gene reveals conserved domains with human ALL-1 and identifies a motif shared with DNA methyltransferases.MLL is fused to CBP, a histone acetyltransferase, in therapy-related acute myeloid leukemia with a t(11;16)(q23;p13.3).Molecular cloning of 19p13 breakpoint region in infantile leukemia with t(11;19)(q23;p13) translocation.Review of Ets1 structure, function, and roles in immunityMammalian neurotrophin-4: structure, chromosomal localization, tissue distribution, and receptor specificity.Molecular cloning of the breakpoints of a complex Philadelphia chromosome translocation: identification of a repeated region on chromosome 17.Molecular cytogenetic delineation of a novel critical genomic region in chromosome bands 11q22.3-923.1 in lymphoproliferative disorders.The (4;11)(q21;q23) chromosome translocations in acute leukemias involve the VDJ recombinase
P2860
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P2860
Mapping chromosome band 11q23 in human acute leukemia with biotinylated probes: identification of 11q23 translocation breakpoints with a yeast artificial chromosome.
description
1990 nî lūn-bûn
@nan
1990 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1990 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
1990年の論文
@ja
1990年論文
@yue
1990年論文
@zh-hant
1990年論文
@zh-hk
1990年論文
@zh-mo
1990年論文
@zh-tw
1990年论文
@wuu
name
Mapping chromosome band 11q23 ...... a yeast artificial chromosome.
@ast
Mapping chromosome band 11q23 ...... a yeast artificial chromosome.
@en
type
label
Mapping chromosome band 11q23 ...... a yeast artificial chromosome.
@ast
Mapping chromosome band 11q23 ...... a yeast artificial chromosome.
@en
prefLabel
Mapping chromosome band 11q23 ...... a yeast artificial chromosome.
@ast
Mapping chromosome band 11q23 ...... a yeast artificial chromosome.
@en
P2093
P2860
P356
P1476
Mapping chromosome band 11q23 ...... a yeast artificial chromosome.
@en
P2093
E van Melle
J D Rowley
J H Kersey
P Taillon-Miller
R Espinosa
P2860
P304
P356
10.1073/PNAS.87.23.9358
P407
P577
1990-12-01T00:00:00Z