Two human c-onc genes are located on the long arm of chromosome 8.
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Human proto-oncogene c-mos maps to 8q11Cerebellar degeneration-related antigen: a highly conserved neuroectodermal marker mapped to chromosomes X in human and mouseInfluence of calorie restriction on oncogene expression and DNA synthesis during liver regenerationInterferon-inducible gene maps to a chromosomal band associated with a (4;11) translocation in acute leukemia cellsHigh-resolution chromosomal localization of human genes for amylase, proopiomelanocortin, somatostatin, and a DNA fragment (D3S1) by in situ hybridizationA human c-erbA oncogene homologue is closely proximal to the chromosome 17 breakpoint in acute promyelocytic leukemiaCooperative antiproliferative effect of coordinated ectopic expression of DLC1 tumor suppressor protein and silencing of MYC oncogene expression in liver cancer cells: Therapeutic implicationsThe short arm of chromosome 11 is a "hot spot" for hypermethylation in human neoplasiaInactivation of MYC reverses tumorigenesis.Mapping of the c-myc, pvt-1 and immunoglobulin kappa genes in relation to the mouse plasmacytoma-associated variant (6;15) translocation breakpoint.Aberrant c-myc RNAs of Burkitt's lymphoma cells have longer half-livesInterchromosomal recombination of the cellular oncogene c-myc with the immunoglobulin heavy chain locus in murine plasmacytomas is a reciprocal exchangeThe second oncogene mil of avian retrovirus MH2 is related to the src gene family.Translocation of an immunoglobulin kappa locus to a region 3' of an unrearranged c-myc oncogene enhances c-myc transcription.The molecular biology of chromosome alterations in myelogenous leukemia.Double minutes arise from circular extrachromosomal DNA intermediates which integrate into chromosomal sites in human HL-60 leukemia cells.Amplification and deregulation of MYC following Epstein-Barr virus infection of a human B-cell lineChromosomal location of the human gene for DNA polymerase beta.Primary structure of c-kit: relationship with the CSF-1/PDGF receptor kinase family--oncogenic activation of v-kit involves deletion of extracellular domain and C terminus.Localization of the beta-globin gene by chromosomal in situ hybridization.The William Allan Memorial Award address: Reverse genetics and beyondLocalization of the restriction fragment length polymorphism D14S1 (pAW-101) to chromosome 14q32.1 leads to 32.2 by in situ hybridization.Cervical cancer: is herpes simplex virus type II a cofactor?Secondary activation of c-abl may be related to translocation to the nucleolar organizer region in an in vitro cultured rat leukemia cell line (K3D)The N-ras oncogene assigned to the short arm of human chromosome 1.Chromosomal localization of the human c-fms oncogeneMapping and gene expression profile of the minimally overrepresented 8q24 region in prostate cancer.Recurrent chromosomal imbalances detected in biopsy material from oral premalignant and malignant lesions by combined tissue microdissection, universal DNA amplification, and comparative genomic hybridizationOver-expression of the c-myc proto-oncogene in colorectal carcinoma.Products of a reciprocal chromosome translocation involving the c-myc gene in a murine plasmacytoma.The 2p breakpoint of a 2;8 translocation in Burkitt lymphoma interrupts the V kappa locus.Orientation of loci within the human major histocompatibility complex by chromosomal in situ hybridization.The HL60 cell line: a model system for studying human myeloid cell differentiation.c-sis is translocated from chromosome 22 to chromosome 9 in chronic myelocytic leukemiaLocalization of cloned unique DNA to three different regions of chromosome 19: screen for linkage probes for myotonic dystrophy.Recent advances in the treatment of acute lymphoblastic leukemia in adults and future prospects.Malignant lymphomas with band 8q24 chromosome abnormality: a morphologic continuum extending from Burkitt's to immunoblastic lymphoma.The structure and nucleotide sequence of the 5' end of the human c-myc oncogene.Structure and expression of the oncogene c-myc in fresh tumor material from patients with hematopoietic malignancies.Polymorphic gene for human carbonic anhydrase II: a molecular disease marker located on chromosome 8.
P2860
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P2860
Two human c-onc genes are located on the long arm of chromosome 8.
description
1982 nî lūn-bûn
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1982年の論文
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1982年学术文章
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1982年学术文章
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1982年学术文章
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1982年学术文章
@zh-my
1982年学术文章
@zh-sg
1982年學術文章
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1982年學術文章
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1982年學術文章
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name
Two human c-onc genes are located on the long arm of chromosome 8.
@ast
Two human c-onc genes are located on the long arm of chromosome 8.
@en
type
label
Two human c-onc genes are located on the long arm of chromosome 8.
@ast
Two human c-onc genes are located on the long arm of chromosome 8.
@en
prefLabel
Two human c-onc genes are located on the long arm of chromosome 8.
@ast
Two human c-onc genes are located on the long arm of chromosome 8.
@en
P2093
P2860
P356
P1476
Two human c-onc genes are located on the long arm of chromosome 8.
@en
P2093
R S Chaganti
S C Jhanwar
W S Hayward
P2860
P304
P356
10.1073/PNAS.79.24.7842
P407
P577
1982-12-01T00:00:00Z