Publication Listing for the MeSH term retinoblastoma. Found 13 abstracts

Knudson AG. A personal sixty-year tour of genetics and medicine. Annual Review of Genomics and Human Genetics. 2005 Jan;6:1-14.

Fujio Y, Guo K, Mano T, Mitsuuchi Y, Testa JR, Walsh K. Cell cycle withdrawal promotes myogenic induction of Akt, a positive modulator of myocyte survival. Mol Cell Biol. 1999 Jul;19(7):5073-82.

Nowell P, Rowley J, Knudson A. Cancer genetics, cytogenetics - defining the enemy within. Nat Med. 1998 Oct;4(10):1107-11.

Knudson AG. Hereditary cancer: Theme and variations. J Clin Oncol. 1997 Oct;15(10):3280-7.

Bianchi AB, Hara T, Ramesh V, Gao JZ, Kleinszanto AJ, Morin F, Menon AG, Trofatter JA, Gusella JF, Seizinger BR, Kley N. Mutations in Transcript Isoforms of the Neurofibromatosis-2 Gene in Multiple Human Tumor Types. Nat Genet. 1994 Feb;6(2):185-92.

Rebbeck TR, Lustbader ED, Buetow KH. Somatic Allele Loss in Genetic-Linkage Analysis of Cancer. Genet Epidemiol. 1994 Jan;11(5):419-29.

Knudson A. Genetics of Tumors of the Head and Neck. Archives of Otolaryngology-Head & Neck Surgery. 1993 Jul;119(7):735-7.

Knudson AG. All in the (Cancer) Family. Nat Genet. 1993 Oct;5(2):103-4.

Knudson AG. Pediatric Molecular Oncology - Past as Prologue to the Future. Cancer. 1993 May 15;71(10):3320-4.

Knudson AG. Introduction to the Genetics of Primary Renal Tumors in Children. Med Pediatr Oncol. 1993 Jan;21(3):193-8.

Godwin AK, Testa JR, Handel LM, Liu Z, Vanderveer LA, Tracey PA, Hamilton TC. Spontaneous Transformation of Rat Ovarian Surface Epithelial- Cells - Association with Cytogenetic Changes and Implications of Repeated Ovulation in the Etiology of Ovarian-Cancer. J Natl Cancer Inst. 1992 Apr 15;84(8):592-601.

Miura I, Graziano SL, Cheng JQ, Doyle LA, Testa JR. Chromosome Alterations in Human Small-Cell Lung-Cancer - Frequent Involvement of 5q. Cancer Res. 1992 Mar;52(5):1322-8.

Ruggeri B, Zhang SY, Caamano J, Dirado M, Flynn SD, Kleinszanto AJ. Human Pancreatic Carcinomas and Cell-Lines Reveal Frequent and Multiple Alterations in the P53 and Rb-1 Tumor-Suppressor Genes. Oncogene. 1992 Aug;7(8):1503-11.

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retinoblastoma mutations expression gene deletion carcinoma sarcoma lines n-myc beckwith-wiedemann syndrome abnormalities tumor suppressor genes breast-cancer wilms tumor cancer mutation amplification heterozygosity chromosome-11 familial monoclonal-antibodies bilateral acoustic neurofibromatosis epidermal growth-factor translocation rhabdoid tumor dependent dna polymerase ataxia-telangiectasia cells burkitt-lymphoma type-1 gene squamous-cell carcinoma chromosome prevention family cancer syndromes nf2 p53 brca1 proliferating myoblasts tsc2 gene somatic genetic mutation induction eker rat model dominantly inherited cancer wilms tumor locus tumors wilms-tumor human papillomavirus type-16 c-myc oncogene chromosome-5 drash syndrome imprinting phosphatidylinositol 3-kinase short arm chromosome-22 pleckstrin homology domain tay-sachs-disease colorectal-cancer leukemia growth factor-ii oncogenes ret protooncogene causation lung-cancer protein treatment alleles ovarian-cancer alpha-interferon polyposis-coli c-akt human prostate carcinoma recombination risk-factors pediatric cancer suppression sequence polyposis beta association osteo- differentiation dna predisposition identification segment lod score skeletal-muscle cells protein-kinase-b transformation cycle heterogeneity regulated expression homolog two hits cancer-genetic chaos loss of heterozygosity human breast-cancer terminal