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Results: 1 to 20 of 398

Similar articles for PubMed (Select 19280657)

1.

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. doi: 10.1002/humu.20940.

PMID:
19280657
2.

Constitutional and somatic RB1 mutation spectrum in nonfamilial unilateral and bilateral retinoblastoma in India.

Bamne MN, Ghule PN, Jose J, Banavali SD, Kurkure PA, Amare Kadam PS.

Genet Test. 2005 Fall;9(3):200-11.

PMID:
16225399
3.

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.

PMID:
12187430
4.

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.

PMID:
18503160
5.

Constitutional RB1-gene mutations in patients with isolated unilateral retinoblastoma.

Lohmann DR, Gerick M, Brandt B, Oelschläger U, Lorenz B, Passarge E, Horsthemke B.

Am J Hum Genet. 1997 Aug;61(2):282-94.

6.

Detection of mutations of the RB1 gene in retinoblastoma patients by using exon-by-exon PCR-SSCP analysis.

Shimizu T, Toguchida J, Kato MV, Kaneko A, Ishizaki K, Sasaki MS.

Am J Hum Genet. 1994 May;54(5):793-800.

7.

Sensitive and efficient detection of RB1 gene mutations enhances care for families with retinoblastoma.

Richter S, Vandezande K, Chen N, Zhang K, Sutherland J, Anderson J, Han L, Panton R, Branco P, Gallie B.

Am J Hum Genet. 2003 Feb;72(2):253-69. Epub 2002 Dec 18.

8.

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.

PMID:
15884040
9.

A comprehensive, sensitive and economical approach for the detection of mutations in the RB1 gene in retinoblastoma.

Parsam VL, Kannabiran C, Honavar S, Vemuganti GK, Ali MJ.

J Genet. 2009 Dec;88(4):517-27.

10.

Hereditary retinoblastoma transmitted by maternal germline mosaicism.

Barbosa RH, Vargas FR, Aguiar FC, Ferman S, Lucena E, Bonvicino CR, Seuánez HN.

Pediatr Blood Cancer. 2008 Nov;51(5):598-602. doi: 10.1002/pbc.21687.

PMID:
18661485
11.

Molecular-genetic analysis of two cases with retinoblastoma: benefits for disease management.

Kumaramanickavel G, Joseph B, Narayana K, Natesh S, Mamatha G, Shanmugam MP, Elamparathi A, Biswas J.

J Genet. 2003 Apr-Aug;82(1-2):39-44.

12.

Comprehensive screening for constitutional RB1 mutations by DHPLC and QMPSF.

Houdayer C, Gauthier-Villars M, Laugé A, Pagès-Berhouet S, Dehainault C, Caux-Moncoutier V, Karczynski P, Tosi M, Doz F, Desjardins L, Couturier J, Stoppa-Lyonnet D.

Hum Mutat. 2004 Feb;23(2):193-202.

PMID:
14722923
13.

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.

PMID:
16343894
14.
15.

A c.1363C>T (p.R455X) nonsense mutation of RB1 gene in a southern Chinese retinoblastoma pedigree.

Chen CY, Xu CM, Du ZF, Chen XL, Ren GL, Zhang XN.

Genet Test Mol Biomarkers. 2010 Apr;14(2):193-6. doi: 10.1089/gtmb.2009.0162.

PMID:
20059380
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. doi: 10.1002/humu.22488. Epub 2013 Dec 20.

17.

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.

PMID:
16682285
18.

RB1 germ-line deletions in Argentine retinoblastoma patients.

Fernández C, Repetto K, Dalamon V, Bergonzi F, Ferreiro V, Szijan I.

Mol Diagn Ther. 2007;11(1):55-61.

PMID:
17286450
19.

Novel RB1 gene constitutional mutations found in Polish patients with familial and/or bilateral retinoblastoma.

Jakubowska A, Zajaczek S, Haus O, Limon J, Kostyk E, Krzystolik Z, Lubinski J.

Hum Mutat. 2001 Nov;18(5):459.

PMID:
11668642
20.

[Low-penetrance retinoblastoma due to exons 24 and 25 deletions in the Rb1 gene].

Du C, Jiang Y, Gallie BL.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2002 Oct;19(5):370-4. Chinese.

PMID:
12362308
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