317 related articles for article (PubMed ID: 2568588)
1. Preferential germline mutation of the paternal allele in retinoblastoma.
Zhu XP; Dunn JM; Phillips RA; Goddard AD; Paton KE; Becker A; Gallie BL
Nature; 1989 Jul; 340(6231):312-3. PubMed ID: 2568588
[TBL] [Abstract][Full Text] [Related]
2. Parental origin of mutations of the retinoblastoma gene.
Dryja TP; Mukai S; Petersen R; Rapaport JM; Walton D; Yandell DW
Nature; 1989 Jun; 339(6225):556-8. PubMed ID: 2733786
[TBL] [Abstract][Full Text] [Related]
3. 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; 48(14):3939-43. PubMed ID: 2898286
[TBL] [Abstract][Full Text] [Related]
4. A molecular study of first and second RB1 mutational hits in retinoblastoma patients.
de Andrade AF; da Hora Barbosa R; Vargas FR; Ferman S; Eisenberg AL; Fernandes L; Bonvicino CR
Cancer Genet Cytogenet; 2006 May; 167(1):43-6. PubMed ID: 16682285
[TBL] [Abstract][Full Text] [Related]
5. The genetics of retinoblastoma.
Stahl A; Levy N; Wadzynska T; Sussan JM; Jourdan-Fonta D; Saracco JB
Ann Genet; 1994; 37(4):172-8. PubMed ID: 7710251
[TBL] [Abstract][Full Text] [Related]
6. Sex mutation ratio in retinoblastoma and retinoma: relevance to genetic counseling.
Munier FL; Thonney F; Balmer A; Héon E; Pescia G; Schorderet DF
Klin Monbl Augenheilkd; 1996 May; 208(5):400-3. PubMed ID: 8766064
[TBL] [Abstract][Full Text] [Related]
7. Unilateral retinoblastoma, lack of familial history and older age does not exclude germline RB1 gene mutation.
Brichard B; Heusterspreute M; De Potter P; Chantrain C; Vermylen C; Sibille C; Gala JL
Eur J Cancer; 2006 Jan; 42(1):65-72. PubMed ID: 16343894
[TBL] [Abstract][Full Text] [Related]
8. 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; 338(6211):156-8. PubMed ID: 2918936
[TBL] [Abstract][Full Text] [Related]
9. RB1 gene mutations in retinoblastoma.
Lohmann DR
Hum Mutat; 1999; 14(4):283-8. PubMed ID: 10502774
[TBL] [Abstract][Full Text] [Related]
10. Sensitive multistep clinical molecular screening of 180 unrelated individuals with retinoblastoma detects 36 novel mutations in the RB1 gene.
Nichols KE; Houseknecht MD; Godmilow L; Bunin G; Shields C; Meadows A; Ganguly A
Hum Mutat; 2005 Jun; 25(6):566-74. PubMed ID: 15884040
[TBL] [Abstract][Full Text] [Related]
11. Identification of three new mutations in the RB1 gene in patients with sporadic retinoblastoma in Colombia.
Serrano ML; Yunis JJ
Biomedica; 2013; 33(1):53-61. PubMed ID: 23715307
[TBL] [Abstract][Full Text] [Related]
12. Loss of heterozygosity and mutations are the major mechanisms of RB1 gene inactivation in Chinese with sporadic retinoblastoma.
Choy KW; Pang CP; Yu CB; Wong HL; Ng JS; Fan DS; Lo KW; Chai JT; Wang J; Fu W; Lam DS
Hum Mutat; 2002 Nov; 20(5):408. PubMed ID: 12402348
[TBL] [Abstract][Full Text] [Related]
13. Identification of four novel RB1 germline mutations in Korean retinoblastoma patients.
Yu YS; Kim IJ; Ku JL; Park JG
Hum Mutat; 2001 Sep; 18(3):252. PubMed ID: 11524739
[TBL] [Abstract][Full Text] [Related]
14. Preferential retention of paternal alleles in human retinoblastoma: evidence for genomic imprinting.
Leach RJ; Magewu AN; Buckley JD; Benedict WF; Rother C; Murphree AL; Griegel S; Rajewsky MF; Jones PA
Cell Growth Differ; 1990 Sep; 1(9):401-6. PubMed ID: 1981144
[TBL] [Abstract][Full Text] [Related]
15. Molecular studies of loss of heterozygosity in Chinese sporadic retinoblastoma patients.
Zhang XL; Fu WL; Zhao HX; Zhou LX; Huang JF; Wang JH
Clin Chim Acta; 2005 Aug; 358(1-2):75-80. PubMed ID: 15921673
[TBL] [Abstract][Full Text] [Related]
16. The molecular genetics of retinoblastoma.
Goodrich DW; Lee WH
Cancer Surv; 1990; 9(3):529-54. PubMed ID: 2101724
[TBL] [Abstract][Full Text] [Related]
17. Detection of mosaic RB1 mutations in families with retinoblastoma.
Rushlow D; Piovesan B; Zhang K; Prigoda-Lee NL; Marchong MN; Clark RD; Gallie BL
Hum Mutat; 2009 May; 30(5):842-51. PubMed ID: 19280657
[TBL] [Abstract][Full Text] [Related]
18. Genome instability in secondary solid tumors developing after radiotherapy of bilateral retinoblastoma.
Lefèvre SH; Vogt N; Dutrillaux AM; Chauveinc L; Stoppa-Lyonnet D; Doz F; Desjardins L; Dutrillaux B; Chevillard S; Malfoy B
Oncogene; 2001 Dec; 20(56):8092-9. PubMed ID: 11781822
[TBL] [Abstract][Full Text] [Related]
19. Improved clinical management of retinoblastoma through gene testing.
Raizis A; Clemett R; Corbett R; McGaughran J; Evans J; George P
N Z Med J; 2002 May; 115(1154):231-4. PubMed ID: 12117173
[TBL] [Abstract][Full Text] [Related]
20. Age at diagnosis of isolated unilateral retinoblastoma does not distinguish patients with and without a constitutional RB1 gene mutation but is influenced by a parent-of-origin effect.
Schüler A; Weber S; Neuhäuser M; Jurklies C; Lehnert T; Heimann H; Rudolph G; Jöckel KH; Bornfeld N; Lohmann DR
Eur J Cancer; 2005 Mar; 41(5):735-40. PubMed ID: 15763650
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
