Retinoblastoma: Clues to Human Oncogenesis

scientific article published on March 9, 1984

Retinoblastoma: Clues to Human Oncogenesis is …
instance of (P31):
scholarly articleQ13442814
review articleQ7318358

External links are
P356DOI10.1126/SCIENCE.6320372
P953full work available at URLhttps://syndication.highwire.org/content/doi/10.1126/science.6320372
P698PubMed publication ID6320372

P2093author name stringW. F. Benedict
A. L. Murphree
P2860cites workJournal of the National Cancer InstituteQ400279
American Journal of Human GeneticsQ4744249
Chromosome number 11 and Wilms' tumorQ72925909
Mutation and cancer: statistical study of retinoblastomaQ24618185
Human-tumor-derived cell lines contain common and different transforming genesQ34245850
T24 human bladder carcinoma oncogene is an activated form of the normal human homologue of BALB- and Harvey-MSV transforming genesQ34253435
Cellular Transforming GenesQ34253517
Expression of recessive alleles by chromosomal mechanisms in retinoblastomaQ34264957
N.A.S. symposium: new evidence as the basis for increased efforts in cancer researchQ34700414
A general theory of carcinogenesisQ34744320
Genetics and the Etiology of Childhood CancerQ37019539
Cellular Oncogenes and Multistep CarcinogenesisQ40161805
Second nonocular tumors in retinoblastoma survivors. Are they radiation-induced?Q40229965
Chromosome 1 in 26 carcinomas of the cervix uteriStructural and numerical changesQ40608870
Hereditary Renal-Cell Carcinoma Associated with a Chromosomal TranslocationQ41751694
Amplified DNA with limited homology to myc cellular oncogene is shared by human neuroblastoma cell lines and a neuroblastoma tumourQ42799715
Correlation Between Balance of Specific Chromosomes and Expression of Malignancy in Hamster Cells 2Q44458293
Chromosome changes in 17 human neoplasms studied with bandingQ44683654
Chromosomes 1 in 14 ovarian cancers. Heterochromatin variants and structural changesQ46226642
Abnormalities of chromosome No. 1 in human solid malignant tumoursQ46929735
Familial Retinoblastoma and Chromosome 13 Deletion Transmitted via an Insertional TranslocationQ53569910
The chromosomal basis of human neoplasia.Q53762162
Nonrandom distribution of chromosomal aberrations induced by three chemicals.Q54565358
Patient with 13 Chromosome Deletion: Evidence That the Retinoblastoma Gene Is a Recessive Cancer GeneQ55062498
Multiple karyotypic changes in retinoblastoma tumor cells: Presence of normal chromosome No. 13 in most tumorsQ58348288
Human breast carcinomas: marker chromosomes involving 1q in seven casesQ68209700
Renal Carcinoma (Hypernephroma) Occurring in 5 SiblingsQ69374279
Human cell hybrids: analysis of transformation and tumorigenicityQ70264695
Familial renal cell carcinoma with a 3;11 chromosome translocation limited to tumor cellsQ70439023
Abnormalities of chromosome #13 in retinoblastomas from individuals with normal constitutional karyotypesQ70448253
High rate of detection of 13q14 deletion mosaicism among retinoblastoma patients (using more extensive methods)Q70480845
Similar chromosomal abnormalities in several retinoblastomasQ70601008
Nonrandom chromosomal changes in untreated retinoblastomasQ71139588
Regional assignment of genes for human esterase D and retinoblastoma to chromosome band 13q14Q71198008
Gene for hereditary retinoblastoma assigned to human chromosome 13 by linkage to esterase DQ71656765
Specific chromosome defect associated with human small-cell lung cancer; deletion 3p(14-23)Q72916321
P433issue4640
P407language of work or nameEnglishQ1860
P921main subjectretinoblastomaQ500695
Suppression, GeneticQ71148826
P304page(s)1028-1033
P577publication date1984-03-01
1984-03-09
P1433published inScienceQ192864
P1476titleRetinoblastoma: clues to human oncogenesis
Retinoblastoma: Clues to Human Oncogenesis
P478volume223

Reverse relations

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