CA50331/CA/NCI NIH HHS/United States[Grant Number] - Search Results

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Year	Number of Results
1993	1
1994	1
1996	1
1997	2
2021	0

Page 1

A splicing mutation in RB1 in low penetrance retinoblastoma.

Schubert EL, Strong LC, Hansen MF. Schubert EL, et al. Hum Genet. 1997 Oct;100(5-6):557-63. doi: 10.1007/s004390050551. Hum Genet. 1997. PMID: 9341870

A previously unknown polymorphism located within the RB1 locus only present in Asian individuals.

Schubert EL, Hansen MF. Schubert EL, et al. Hum Hered. 1996 Mar-Apr;46(2):118-20. doi: 10.1159/000154338. Hum Hered. 1996. PMID: 8666413

Concordance between parental origin of chromosome 13q loss and chromosome 6p duplication in sporadic retinoblastoma.

Naumova A, Hansen M, Strong L, Jones PA, Hadjistilianou D, Mastrangelo D, Griegel S, Rajewsky MF, Shields J, Donoso L, et al. Naumova A, et al. Am J Hum Genet. 1994 Feb;54(2):274-81. Am J Hum Genet. 1994. PMID: 8304344 Free PMC article.

A method to isolate DNA from small archival tissue samples for p53 gene analysis.

Schubert EL, Bischoff FZ, Whitaker LL, Pleasants LM, Hansen MF. Schubert EL, et al. Hum Mutat. 1993;2(2):123-6. doi: 10.1002/humu.1380020211. Hum Mutat. 1993. PMID: 8318988

Induction of apoptosis in Mv1Lu cells by expression of competitive RB1 mutants.

Whitaker LL, Hansen MF. Whitaker LL, et al. Oncogene. 1997 Aug 28;15(9):1069-77. doi: 10.1038/sj.onc.1201277. Oncogene. 1997. PMID: 9285561

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