Molecular etiology of low-penetrance retinoblastoma in two pedigrees.
about
Apoptosis induced by the nuclear death domain protein p84N5 is inhibited by association with Rb proteinNegative regulation of DNA replication by the retinoblastoma protein is mediated by its association with MCM7.RB1 gene mutation up-date, a meta-analysis based on 932 reported mutations available in a searchable database.A knowledge network for a dynamic taxonomy of psychiatric diseaseCrystal Structure of the Retinoblastoma Protein N Domain Provides Insight into Tumor Suppression, Ligand Interaction, and Holoprotein ArchitectureGenetic interaction between Rb and K-ras in the control of differentiation and tumor suppressionThe N Terminus of the Retinoblastoma Protein Inhibits DNA Replication via a Bipartite Mechanism Disrupted in Partially Penetrant Retinoblastomas.Recent advances in the gene map of inherited eye disorders: primary hereditary diseases of the retina, choroid, and vitreous.Low penetrance of retinoblastoma for p.V654L mutation of the RB1 gene.The retinoblastoma protein is linked to the activation of Ras.Temperature-sensitive RB mutations linked to incomplete penetrance of familial retinoblastoma in 12 families.Are there low-penetrance TP53 Alleles? evidence from childhood adrenocortical tumorsTumor suppression by a severely truncated species of retinoblastoma protein.Frequency of somatic and germ-line mosaicism in retinoblastoma: implications for genetic counseling.Functional interactions between the retinoblastoma (Rb) protein and Sp-family members: superactivation by Rb requires amino acids necessary for growth suppression.Stable binding to E2F is not required for the retinoblastoma protein to activate transcription, promote differentiation, and suppress tumor cell growth.Constitutional RB1-gene mutations in patients with isolated unilateral retinoblastoma.Deletion of RB exons 24 and 25 causes low-penetrance retinoblastomaThe genetics of retinoblastoma, revisitedThe RB1 gene mutation in a child with ectopic intracranial retinoblastomaMutations of N-terminal regions render the retinoblastoma protein insufficient for functions in development and tumor suppression.Incomplete penetrance of familial retinoblastoma linked to germ-line mutations that result in partial loss of RB functionLow-penetrant RB allele in small-cell cancer shows geldanamycin instability and discordant expression with mutant rasGermline mutations in retinoma patients: relevance to low-penetrance and low-expressivity molecular basis.Bimodal expressivity in dominant retinitis pigmentosa genetically linked to chromosome 19q.RB1 gene mutations in Argentine retinoblastoma patients. Implications for genetic counseling.
P2860
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P2860
Molecular etiology of low-penetrance retinoblastoma in two pedigrees.
description
1993 nî lūn-bûn
@nan
1993 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
1993 թվականի հունիսին հրատարակված գիտական հոդված
@hy
1993年の論文
@ja
1993年論文
@yue
1993年論文
@zh-hant
1993年論文
@zh-hk
1993年論文
@zh-mo
1993年論文
@zh-tw
1993年论文
@wuu
name
Molecular etiology of low-penetrance retinoblastoma in two pedigrees.
@ast
Molecular etiology of low-penetrance retinoblastoma in two pedigrees.
@en
type
label
Molecular etiology of low-penetrance retinoblastoma in two pedigrees.
@ast
Molecular etiology of low-penetrance retinoblastoma in two pedigrees.
@en
prefLabel
Molecular etiology of low-penetrance retinoblastoma in two pedigrees.
@ast
Molecular etiology of low-penetrance retinoblastoma in two pedigrees.
@en
P2093
P2860
P1476
Molecular etiology of low-penetrance retinoblastoma in two pedigrees
@en
P2093
P2860
P304
P407
P577
1993-06-01T00:00:00Z