scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1053199984 |
P356 | DOI | 10.1038/310325A0 |
P698 | PubMed publication ID | 6462218 |
P2093 | author name string | F Mitelman | |
P2860 | cites work | Mapping of human chromosomal regions related to neoplasia: Evidence from chromosomes 1 and 17 | Q35054247 |
Gene-amplification model of carcinogenesis | Q35351306 | ||
The origin of human cancers | Q40123412 | ||
Report of the committee on chromosome rearrangements in neoplasia and on fragile sites | Q40166075 | ||
Clustering of aberrations to specific chromosomes in human neoplasms. IV. A survey of 1,871 cases | Q40325966 | ||
Clustering of aberrations to specific chromosomes in human neoplasms. III. Incidence and geographic distribution of chromosome aberrations in 856 cases | Q44160745 | ||
The role of gene dosage and genetic transpositions in carcinogenesis | Q53569200 | ||
Onco gen: Human oncogene locations and chromosome aberrations | Q59071123 | ||
Translocation of c-abl oncogene correlates with the presence of a Philadelphia chromosome in chronic myelocytic leukaemia | Q59085791 | ||
An international system for human cytogenetic nomenclature (1978) ISCN (1978). Report of the Standing Commitee on Human Cytogenetic Nomenclature | Q67446121 | ||
Catalogue of chromosome aberrations in cancer | Q71065155 | ||
P433 | issue | 5975 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | leukemia | Q29496 |
P304 | page(s) | 325-327 | |
P577 | publication date | 1984-07-01 | |
P1433 | published in | Nature | Q180445 |
P1476 | title | Restricted number of chromosomal regions implicated in aetiology of human cancer and leukaemia | |
P478 | volume | 310 |
Q84535070 | A GOG 210 aCGH study of gain at 1q23 in endometrioid endometrial cancer in the context of racial disparity and outcome |
Q36727428 | A novel, plasmid-based system for studying gene rearrangements in mammalian cells |
Q44689785 | Aberrant breakpoints in chronic myelogenous leukaemia; oncogenes and fragile sites. |
Q41216899 | Application of log-linear model in inference on karyotypic evolution in chronic myelocytic leukemia |
Q37686616 | Assignment of the gene coding for the T3-delta subunit of the T3-T-cell receptor complex to the long arm of human chromosome 11 and to mouse chromosome 9. |
Q50536128 | Chromosomal insertion of human papillomavirus 18 sequences in HeLa cells detected by nonisotopic in situ hybridization and reflection contrast microscopy. |
Q37559044 | Chromosomal localization and characterization of c-abl in the t(6;9) of acute nonlymphocytic leukemia |
Q52828811 | Chromosome changes in human monocytic cell lines with in vitro spontaneous malignant transformation. |
Q54253017 | Chromosome study of five cancers of the prostate. |
Q34559025 | Cloning and structural analysis of cDNAs for bcl-2 and a hybrid bcl-2/immunoglobulin transcript resulting from the t(14;18) translocation |
Q38878855 | Cytogenetic characterization of several androgen responsive and unresponsive sublines of the human prostatic carcinoma cell line LNCaP. |
Q68990600 | DNA-abnormality in hairy cell leukemia |
Q74570927 | Detection of chromosome over- and underrepresentations in hyperdiploid acute lymphoblastic leukemia by comparative genomic hybridization |
Q68309251 | Evidence for the clonal nature of hypereosinophilic syndrome |
Q24568213 | Identification of a single chromosome in the normal human genome essential for suppression of hamster cell transformation |
Q24611533 | Interferon-inducible gene maps to a chromosomal band associated with a (4;11) translocation in acute leukemia cells |
Q35976936 | Karyotypic abnormalities in tumours of the pancreas |
Q77207982 | Localization of chromosome breakpoints: implication of the chromatin structure and nuclear architecture |
Q36472629 | Non-random distribution of Alu-family repeats in human chromosomes |
Q70030393 | Oncogenes and the mammalian X chromosome |
Q24675587 | Regional localization of the human transferrin receptor gene to 3q26.2----qter |
Q39760709 | The cellular ets genes: molecular biology and clinical implications in human leukemias |
Q68675753 | The occurrence of variant Ph translocations in chronic myeloid leukemia (CML): a report of six cases |