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Items: 1 to 20 of 143

1.

A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma.

Friend SH, Bernards R, Rogelj S, Weinberg RA, Rapaport JM, Albert DM, Dryja TP.

Nature. 1986 Oct 16-22;323(6089):643-6.

PMID:
2877398
2.

Deletions of a DNA sequence in retinoblastomas and mesenchymal tumors: organization of the sequence and its encoded protein.

Friend SH, Horowitz JM, Gerber MR, Wang XF, Bogenmann E, Li FP, Weinberg RA.

Proc Natl Acad Sci U S A. 1987 Dec;84(24):9059-63. Erratum in: Proc Natl Acad Sci U S A 1988 Apr;85(7):2234.

3.

Genetic sequences that predispose to retinoblastoma and osteosarcoma.

Dryja TP, Friend S, Weinberg RA.

Symp Fundam Cancer Res. 1986;39:115-9.

PMID:
3480547
4.

Molecular detection of deletions involving band q14 of chromosome 13 in retinoblastomas.

Dryja TP, Rapaport JM, Joyce JM, Petersen RA.

Proc Natl Acad Sci U S A. 1986 Oct;83(19):7391-4.

5.

Structural evidence for the authenticity of the human retinoblastoma gene.

Fung YK, Murphree AL, T'Ang A, Qian J, Hinrichs SH, Benedict WF.

Science. 1987 Jun 26;236(4809):1657-61.

PMID:
2885916
6.

Expression of recessive alleles by chromosomal mechanisms in retinoblastoma.

Cavenee WK, Dryja TP, Phillips RA, Benedict WF, Godbout R, Gallie BL, Murphree AL, Strong LC, White RL.

Nature. 1983 Oct 27-Nov 2;305(5937):779-84.

PMID:
6633649
7.

Human retinoblastoma susceptibility gene: cloning, identification, and sequence.

Lee WH, Bookstein R, Hong F, Young LJ, Shew JY, Lee EY.

Science. 1987 Mar 13;235(4794):1394-9.

PMID:
3823889
8.

Somatic events unmask recessive cancer genes to initiate malignancy.

Gallie BL, Worton RG.

J Cell Biochem. 1986;32(3):215-22. Review.

PMID:
3023409
9.

Osteosarcoma and retinoblastoma: a shared chromosomal mechanism revealing recessive predisposition.

Hansen MF, Koufos A, Gallie BL, Phillips RA, Fodstad O, Brøgger A, Gedde-Dahl T, Cavenee WK.

Proc Natl Acad Sci U S A. 1985 Sep;82(18):6216-20.

10.

Chromosome 13 homozygosity in osteosarcoma without retinoblastoma.

Dryja TP, Rapaport JM, Epstein J, Goorin AM, Weichselbaum R, Koufos A, Cavenee WK.

Am J Hum Genet. 1986 Jan;38(1):59-66.

11.

One hundred years of retinoblastoma research. From the clinic to the gene and back again.

Cowell JK.

Ophthalmic Paediatr Genet. 1989 Jun;10(2):75-88. Review.

PMID:
2571113
12.

Human retinoblastoma susceptibility gene: genomic organization and analysis of heterozygous intragenic deletion mutants.

Bookstein R, Lee EY, To H, Young LJ, Sery TW, Hayes RC, Friedmann T, Lee WH.

Proc Natl Acad Sci U S A. 1988 Apr;85(7):2210-4.

13.

Preferential mutation of paternally derived RB gene as the initial event in sporadic osteosarcoma.

Toguchida J, Ishizaki K, Sasaki MS, Nakamura Y, Ikenaga M, Kato M, Sugimot M, Kotoura Y, Yamamuro T.

Nature. 1989 Mar 9;338(6211):156-8.

PMID:
2918936
14.

Chromosome 13 alterations in osteosarcoma cell lines derived from a patient with previous retinoblastoma.

Hovig E, Lothe R, Farrants G, Brøgger A, Fodstad O, Børresen AL.

Cancer Genet Cytogenet. 1991 Nov;57(1):31-40.

PMID:
1684533
15.

Assignment of common allele loss in osteosarcoma to the subregion 17p13.

Toguchida J, Ishizaki K, Nakamura Y, Sasaki MS, Ikenaga M, Kato M, Sugimoto M, Kotoura Y, Yamamuro T.

Cancer Res. 1989 Nov 15;49(22):6247-51.

16.

Retinoblastoma: clues to human oncogenesis.

Murphree AL, Benedict WF.

Science. 1984 Mar 9;223(4640):1028-33. Review.

PMID:
6320372
17.

Chromosomal reorganization for the expression of recessive mutation of retinoblastoma susceptibility gene in the development of osteosarcoma.

Toguchida J, Ishizaki K, Sasaki MS, Ikenaga M, Sugimoto M, Kotoura Y, Yamamuro T.

Cancer Res. 1988 Jul 15;48(14):3939-43.

18.

Some retinoblastomas, osteosarcomas, and soft tissue sarcomas may share a common etiology.

Weichselbaum RR, Beckett M, Diamond A.

Proc Natl Acad Sci U S A. 1988 Apr;85(7):2106-9.

19.

The molecular basis of retinoblastomas.

Weinberg RA.

Ciba Found Symp. 1989;142:99-105; discussion 106-11.

PMID:
2743837
20.

Detection of submicroscopic deletions and a DNA polymorphism at the retinoblastoma locus.

Horsthemke B, Greger V, Barnert HJ, Höpping W, Passarge E.

Hum Genet. 1987 Jul;76(3):257-61.

PMID:
2885256
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