Common fragile sites, extremely large genes, neural development and cancer.
about
Strong association of de novo copy number mutations with autismA common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autismMate-Pair Sequencing as a Powerful Clinical Tool for the Characterization of Cancers with a DNA Viral EtiologyNew insights into the generation and role of de novo mutations in health and diseaseThe landscape of somatic copy-number alteration across human cancers.Verification of genes differentially expressed in neuroblastoma tumours: a study of potential tumour suppressor genesEvaluation of microsatellite variation in the 1000 Genomes Project pilot studies is indicative of the quality and utility of the raw data and alignments.A whole genome association study of mother-to-child transmission of HIV in Malawi.A CTNNA3 compound heterozygous deletion implicates a role for αT-catenin in susceptibility to autism spectrum disorderHigh-resolution genomic profiling of an adult Wilms' tumor: evidence for a pathogenesis distinct from corresponding pediatric tumors.WWOX protein expression in normal human tissues.Disabled-1 alternative splicing in human fetal retina and neural tumors.Ligand regulation of retinoic acid receptor-related orphan receptors: implications for development of novel therapeuticsParkin enhances the expression of cyclin-dependent kinase 6 and negatively regulates the proliferation of breast cancer cellsGenistein suppresses prostate cancer growth through inhibition of oncogenic microRNA-151.Are common fragile sites merely structural domains or highly organized "functional" units susceptible to oncogenic stress?Rescue from replication stress during mitosis.Genetic or epigenetic silencing of low density lipoprotein receptor-related protein 1B expression in oral squamous cell carcinoma.Retinoid-related Orphan Receptors (RORs): Roles in Cellular Differentiation and Development.Genomic instability in induced stem cellsRetinoid-related orphan receptors (RORs): critical roles in development, immunity, circadian rhythm, and cellular metabolismDeletion at fragile sites is a common and early event in Barrett's esophagus.Large transcription units unify copy number variants and common fragile sites arising under replication stressBreakpoint mapping of 13 large parkin deletions/duplications reveals an exon 4 deletion and an exon 7 duplication as founder mutations.NF-κB induces miR-148a to sustain TGF-β/Smad signaling activation in glioblastoma.Loss of p53 in quaking viable mice leads to Purkinje cell defects and reduced survival.Identification of candidate genes for alcohol preference by expression profiling of congenic rat strains.The epigenetic processes of meiosis in male mice are broadly affected by the widely used herbicide atrazine.Slow endocytosis of the LDL receptor-related protein 1B: implications for a novel cytoplasmic tail conformation.NGS-based approach to determine the presence of HPV and their sites of integration in human cancer genome.Genomic instability in the PARK2 locus is associated with Parkinson's disease.Gastrointestinal adenocarcinomas of the esophagus, stomach, and colon exhibit distinct patterns of genome instability and oncogenesis.Somatic copy number alterations in gastric adenocarcinomas among Asian and Western patients.Cancer risk in patients with constitutional chromosome deletions: a nationwide British cohort study.Genomic mechanisms underlying PARK2 large deletions identified in a cohort of patients with PD.The papillomavirus E2 proteinsHow unfinished business from S-phase affects mitosis and beyondMR Imaging Findings in Xp21.2 Duplication Syndrome.Evolving 'omics' technologies for diagnostics of head and neck cancer.Genome-wide catalogue of chromosomal aberrations in barrett's esophagus and esophageal adenocarcinoma: a high-density single nucleotide polymorphism array analysis.
P2860
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P2860
Common fragile sites, extremely large genes, neural development and cancer.
description
2005 nî lūn-bûn
@nan
2005 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
Common fragile sites, extremely large genes, neural development and cancer.
@ast
Common fragile sites, extremely large genes, neural development and cancer.
@en
Common fragile sites, extremely large genes, neural development and cancer.
@nl
type
label
Common fragile sites, extremely large genes, neural development and cancer.
@ast
Common fragile sites, extremely large genes, neural development and cancer.
@en
Common fragile sites, extremely large genes, neural development and cancer.
@nl
prefLabel
Common fragile sites, extremely large genes, neural development and cancer.
@ast
Common fragile sites, extremely large genes, neural development and cancer.
@en
Common fragile sites, extremely large genes, neural development and cancer.
@nl
P2093
P1433
P1476
Common fragile sites, extremely large genes, neural development and cancer.
@en
P2093
David I Smith
Robert Kuhn
Sarah McAvoy
P356
10.1016/J.CANLET.2005.06.049
P407
P577
2005-10-10T00:00:00Z