about
Comparative analysis of function and interaction of transcription factors in nematodes: extensive conservation of orthology coupled to rapid sequence evolutionRetinoblastomaSensitive and efficient detection of RB1 gene mutations enhances care for families with retinoblastomaRB1 gene mutation up-date, a meta-analysis based on 932 reported mutations available in a searchable database.The tumor suppressor gene retinoblastoma-1 is required for retinotectal development and visual function in zebrafishRealizing the promise of cancer predisposition genes.Single nucleotide polymorphism detection by combinatorial fluorescence energy transfer tags and biotinylated dideoxynucleotides.Disruption of chromosome 11 in canine fibrosarcomas highlights an unusual variability of CDKN2B in dogs.Genes and environment: effects on the development of second malignancies in retinoblastoma survivors.Saccharomyces cerevisiae as a model system to define the chromosomal instability phenotype.Paradoxical instability-activity relationship defines a novel regulatory pathway for retinoblastoma proteins.Models of carcinogenesis: an overview.Molecular nature of 11 spontaneous de novo mutations in Drosophila melanogaster.Mutation spectrum of RB1 gene in unilateral retinoblastoma cases from Tunisia and correlations with clinical features.Mainstreaming genetic testing of cancer predisposition genes.Identification of three novel RB1 mutations in Brazilian patients with retinoblastoma by "exon by exon" PCR mediated SSCP analysisMutational analysis of the RB1 gene in Moroccan patients with retinoblastoma.Structure-function analysis of the retinoblastoma tumor suppressor protein - is the whole a sum of its parts?Evidence for autoregulation and cell signaling pathway regulation from genome-wide binding of the Drosophila retinoblastoma protein.Single-nucleotide polymorphisms in the RB1 gene and association with breast cancer in the British populationHallmarks of alternative splicing in cancer.RB1 mutations and second primary malignancies after hereditary retinoblastoma.Haploinsufficiency of p18(INK4c) sensitizes mice to carcinogen-induced tumorigenesis.A cancer derived mutation in the retinoblastoma gene with a distinct defect for LXCXE dependent interactions.Folding of a cyclin box: linking multitarget binding to marginal stability, oligomerization, and aggregation of the retinoblastoma tumor suppressor AB pocket domainScreening for large rearrangements of the RB1 gene in Iranian patients with retinoblastoma using multiplex ligation-dependent probe amplification.Modulators of alternative splicing as novel therapeutics in cancer.RB1 gene mutations in Argentine retinoblastoma patients. Implications for genetic counseling.Detection of APC mosaicism by next-generation sequencing in an FAP patient.Genetic screening in Iranian patients with retinoblastoma.Mutational analyses of RB and BRCA2 as candidate tumour suppressor genes in parathyroid carcinomaRetinoblastomaMolecular Diagnostics in Clinical Oncology
P2860
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P2860
description
1999 nî lūn-bûn
@nan
1999 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
RB1 gene mutations in retinoblastoma.
@ast
RB1 gene mutations in retinoblastoma.
@en
type
label
RB1 gene mutations in retinoblastoma.
@ast
RB1 gene mutations in retinoblastoma.
@en
prefLabel
RB1 gene mutations in retinoblastoma.
@ast
RB1 gene mutations in retinoblastoma.
@en
P1433
P1476
RB1 gene mutations in retinoblastoma.
@en
P2093
Lohmann DR
P304
P356
10.1002/(SICI)1098-1004(199910)14:4<283::AID-HUMU2>3.3.CO;2-A
P577
1999-01-01T00:00:00Z