195 related articles for article (PubMed ID: 19491728)
1. Molecular karyotype of sporadic unilateral retinoblastoma tumors.
Ganguly A; Nichols KE; Grant G; Rappaport E; Shields C
Retina; 2009; 29(7):1002-12. PubMed ID: 19491728
[TBL] [Abstract][Full Text] [Related]
2. High resolution SNP array profiling identifies variability in retinoblastoma genome stability.
Mol BM; Massink MP; van der Hout AH; Dommering CJ; Zaman JM; Bosscha MI; Kors WA; Meijers-Heijboer HE; Kaspers GJ; Riele Ht; Moll AC; Cloos J; Dorsman JC
Genes Chromosomes Cancer; 2014 Jan; 53(1):1-14. PubMed ID: 24249257
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Constitutional genomic instability, chromosome aberrations in tumor cells and retinoblastoma.
Amare Kadam PS; Ghule P; Jose J; Bamne M; Kurkure P; Banavali S; Sarin R; Advani S
Cancer Genet Cytogenet; 2004 Apr; 150(1):33-43. PubMed ID: 15041221
[TBL] [Abstract][Full Text] [Related]
5. RB1 gene inactivation by chromothripsis in human retinoblastoma.
McEvoy J; Nagahawatte P; Finkelstein D; Richards-Yutz J; Valentine M; Ma J; Mullighan C; Song G; Chen X; Wilson M; Brennan R; Pounds S; Becksfort J; Huether R; Lu C; Fulton RS; Fulton LL; Hong X; Dooling DJ; Ochoa K; Mardis ER; Wilson RK; Easton J; Zhang J; Downing JR; Ganguly A; Dyer MA
Oncotarget; 2014 Jan; 5(2):438-50. PubMed ID: 24509483
[TBL] [Abstract][Full Text] [Related]
6. Spectrum of RB1 gene mutations and loss of heterozygosity in Mexican patients with retinoblastoma: identification of six novel mutations.
Macías M; Dean M; Atkinson A; Jiménez-Morales S; García-Vazquez FJ; Saldaña-Alvarez Y; Ramírez-Bello J; Chávez M; Orozco L
Cancer Biomark; 2008; 4(2):93-9. PubMed ID: 18503160
[TBL] [Abstract][Full Text] [Related]
7. Uncommon RB1 somatic mutations in a unilateral retinoblastoma patient.
Ottaviani D; Alonso C; Szijan I
Medicina (B Aires); 2015; 75(3):137-41. PubMed ID: 26117602
[TBL] [Abstract][Full Text] [Related]
8.
Price EA; Patel R; Scheimberg I; Kotiloglu Karaa E; Sagoo MS; Reddy MA; Onadim Z
Ophthalmic Genet; 2021 Oct; 42(5):604-611. PubMed ID: 34003079
[No Abstract] [Full Text] [Related]
9. Linkage analysis and detection of somatic, postzygous RB1 mutations in Serbian retinoblastoma patients.
Kontic M; Palacios I; Kontic M; Alonso J; Pestana A
J BUON; 2011; 16(1):142-6. PubMed ID: 21674866
[TBL] [Abstract][Full Text] [Related]
10. Spectrum of germline
Rojanaporn D; Boontawon T; Chareonsirisuthigul T; Thanapanpanich O; Attaseth T; Saengwimol D; Anurathapan U; Sujirakul T; Kaewkhaw R; Hongeng S
Mol Vis; 2018; 24():778-788. PubMed ID: 30636860
[TBL] [Abstract][Full Text] [Related]
11. Spectrum of RB1 mutations identified in 403 retinoblastoma patients.
Price EA; Price K; Kolkiewicz K; Hack S; Reddy MA; Hungerford JL; Kingston JE; Onadim Z
J Med Genet; 2014 Mar; 51(3):208-14. PubMed ID: 24225018
[TBL] [Abstract][Full Text] [Related]
12. Risk assessment of recurrence in sporadic retinoblastoma using a molecular-based algorithm.
Tran HV; Schorderet DF; Gaillard MC; Balmer A; Munier FL
Ophthalmic Genet; 2012 Mar; 33(1):6-11. PubMed ID: 22103627
[TBL] [Abstract][Full Text] [Related]
13. Characterisation of retinoblastomas without RB1 mutations: genomic, gene expression, and clinical studies.
Rushlow DE; Mol BM; Kennett JY; Yee S; Pajovic S; Thériault BL; Prigoda-Lee NL; Spencer C; Dimaras H; Corson TW; Pang R; Massey C; Godbout R; Jiang Z; Zacksenhaus E; Paton K; Moll AC; Houdayer C; Raizis A; Halliday W; Lam WL; Boutros PC; Lohmann D; Dorsman JC; Gallie BL
Lancet Oncol; 2013 Apr; 14(4):327-34. PubMed ID: 23498719
[TBL] [Abstract][Full Text] [Related]
14. High incidence of allelic loss at 16q12.2 region spanning RBL2/p130 gene in retinoblastoma.
Priya K; Jada SR; Quah BL; Quah TC; Lai PS
Cancer Biol Ther; 2009 Apr; 8(8):714-7. PubMed ID: 19252413
[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. Enhanced sensitivity for detection of low-level germline mosaic RB1 mutations in sporadic retinoblastoma cases using deep semiconductor sequencing.
Chen Z; Moran K; Richards-Yutz J; Toorens E; Gerhart D; Ganguly T; Shields CL; Ganguly A
Hum Mutat; 2014 Mar; 35(3):384-91. PubMed ID: 24282159
[TBL] [Abstract][Full Text] [Related]
17. Profiling genomic copy number changes in retinoblastoma beyond loss of RB1.
Bowles E; Corson TW; Bayani J; Squire JA; Wong N; Lai PB; Gallie BL
Genes Chromosomes Cancer; 2007 Feb; 46(2):118-29. PubMed ID: 17099872
[TBL] [Abstract][Full Text] [Related]
18. Mutational analysis of the RB1 gene in Indian patients with retinoblastoma.
Ata-ur-Rasheed M; Vemuganti Gk; Honavar Sg; Ahmed N; Hasnain Se; Kannabiran C
Ophthalmic Genet; 2002 Jun; 23(2):121-8. PubMed ID: 12187430
[TBL] [Abstract][Full Text] [Related]
19. Comparative genomic hybridization of 49 primary retinoblastoma tumors identifies chromosomal regions associated with histopathology, progression, and patient outcome.
Lillington DM; Kingston JE; Coen PG; Price E; Hungerford J; Domizio P; Young BD; Onadim Z
Genes Chromosomes Cancer; 2003 Feb; 36(2):121-8. PubMed ID: 12508240
[TBL] [Abstract][Full Text] [Related]
20. Screening for RB1 mutations in tumor tissue using denaturing high performance liquid chromatography, multiplex ligation-dependent probe amplification, and loss of heterozygosity analysis.
Sellner LN; Edkins E; Smith N
Pediatr Dev Pathol; 2006; 9(1):31-7. PubMed ID: 16808635
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]