about
Human inositol 1,4,5-trisphosphate type-1 receptor, InsP3R1: structure, function, regulation of expression and chromosomal localizationCardiopulmonary function in two human disorders of the hypoxia-inducible factor (HIF) pathway: von Hippel-Lindau disease and HIF-2alpha gain-of-function mutationThe R22X mutation of the SDHD gene in hereditary paraganglioma abolishes the enzymatic activity of complex II in the mitochondrial respiratory chain and activates the hypoxia pathwayYeast MIG1 repressor is related to the mammalian early growth response and Wilms' tumour finger proteinsAmplification of the human dihydrofolate reductase gene via double minutes is initiated by chromosome breaksLoss of allelic heterozygosity at a second locus on chromosome 11 in sporadic Wilms' tumor cells.Skin fibroblasts from individuals hemizygous for the familial adenopolyposis susceptibility gene show delayed crisis in vitro.Genetics and biochemistry of collagen binding-triggered glandular differentiation in a human colon carcinoma cell line.The short arm of chromosome 11 is a "hot spot" for hypermethylation in human neoplasiaEncephalocraniocutaneous lipomatosis with a mutation in the NF1 gene.Neuronal migration disorders in humans and in mouse models--an overview.Nonrandom duplication of the chromosome bearing a mutated Ha-ras-1 allele in mouse skin tumors.Induction of multiple independent T-cell lymphomas in rats inoculated with MOloney murine leukemia virus.Induced rates of mitotic crossing over and possible mitotic gene conversion per wing anlage cell in Drosophila melanogaster by X rays and fission neutrons.Retinoids and ovarian cancer.Cortical malformations and epilepsy.Genetic screening analysis of patients with hereditary diffuse gastric cancer from northern and northeastern Brazil.Specific chromosomal abnormalities characterize fibrosarcomas of bovine papillomavirus type 1 transgenic mice.Differential DNA sequence deletions from chromosomes 3, 11, 13, and 17 in squamous-cell carcinoma, large-cell carcinoma, and adenocarcinoma of the human lungStructural alterations of DNA ligase I in Bloom syndromeFine mapping of an imprinted gene for familial nonchromaffin paragangliomas, on chromosome 11q23.Ocular manifestations of von Hippel-Lindau disease: clinical and genetic investigations.Stability of genomic imprinting in human induced pluripotent stem cells.A targeted mutation in the mouse E-cadherin gene results in defective preimplantation developmentThyroid hormone receptor mutations in cancer and resistance to thyroid hormone: perspective and prognosisGenetic linkage of Beckwith-Wiedemann syndrome to 11p15.Allelic deletion and mutation of the von Hippel-Lindau (VHL) tumor suppressor gene in pancreatic microcystic adenomas.High-throughput detection of aberrant imprint methylation in the ovarian cancer by the bisulphite PCR-Luminex methodA novel target cell for c-fos-induced oncogenesis: development of chondrogenic tumours in embryonic stem cell chimeras.Congenital abnormalities in children with cancer and their relatives: results from a case-control study (IRESCC)Familial testicular cancer: a report of the UK family register, estimation of risk and an HLA class 1 sib-pair analysis.Retinoblastoma and hypochondroplasia: a case report of two germline mutations arising simultaneously.The normal human H-ras1 gene can act as an onco-suppressor.Mutations of K-ras oncogene in human adrenal tumours in Taiwan.Restriction fragment length polymorphisms of L-myc and myb in human leukaemia and lymphoma in relation to age-selected controls.Hypermethylation of the 5' CpG island of the gene encoding the serine protease Testisin promotes its loss in testicular tumorigenesis.Cell-heritable stages of tumor progression in transgenic mice harboring the bovine papillomavirus type 1 genome.ras effector loop mutations that dissociate p120GAP and neurofibromin interactions.Requirement for the simian virus 40 small tumor antigen in tumorigenesis in transgenic miceRecombination between two integrated proviruses, one of which was inserted near c-myc in a retrovirus-induced rat thymoma: implications for tumor progression.
P2860
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P2860
description
1986 nî lūn-bûn
@nan
1986年の論文
@ja
1986年論文
@yue
1986年論文
@zh-hant
1986年論文
@zh-hk
1986年論文
@zh-mo
1986年論文
@zh-tw
1986年论文
@wuu
1986年论文
@zh
1986年论文
@zh-cn
name
Genetics of human cancer.
@en
type
label
Genetics of human cancer.
@en
prefLabel
Genetics of human cancer.
@en
P1476
Genetics of human cancer.
@en
P2093
Knudson AG Jr
P304
P356
10.1146/ANNUREV.GE.20.120186.001311
P577
1986-01-01T00:00:00Z