Pages that link to "Q33853617"
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The following pages link to Tumor-specific loss of 11p15.5 alleles in del11p13 Wilms tumor and in familial adrenocortical carcinoma (Q33853617):
Displaying 50 items.
- Isolation, characterization, and expression of the murine Wilms' tumor gene (WT1) during kidney development (Q24607161) (← links)
- Transcriptional map of 170-kb region at chromosome 11p15.5: Identification and mutational analysis of the BWR1A gene reveals the presence of mutations in tumor samples (Q24681580) (← links)
- Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping (Q28236877) (← links)
- WT1 expression induces features of renal epithelial differentiation in mesenchymal fibroblasts (Q28505651) (← links)
- Tumor-suppressor genes: cardinal factors in inherited predisposition to human cancers (Q30499489) (← links)
- Microdissection of chromosome band 11 p 15.5: Characterization of probes mapping distal to theHBBC locus (Q33246532) (← links)
- Loss of the eukaryotic initiation factor 3f in pancreatic cancer (Q33301656) (← links)
- Paternally inherited duplications of 11p15.5 and Beckwith-Wiedemann syndrome (Q33679562) (← links)
- Adrenal cancer (Q33872479) (← links)
- The parathyroid hormone-responsive B1 gene is interrupted by a t(1;7)(q42;p15) breakpoint associated with Wilms' tumour (Q34181512) (← links)
- The human MyoD1 (MYF3) gene maps on the short arm of chromosome 11 but is not associated with the WAGR locus or the region for the Beckwith-Wiedemann syndrome (Q34200750) (← links)
- Silencing of imprinted CDKN1C gene expression is associated with loss of CpG and histone H3 lysine 9 methylation at DMR-LIT1 in esophageal cancer (Q34303935) (← links)
- Genetic predisposition to cancer and familial cancer syndromes (Q34438119) (← links)
- Uniparental paternal disomy in a genetic cancer-predisposing syndrome (Q34535432) (← links)
- Loss of heterozygosity mapping in Wilms tumor indicates the involvement of three distinct regions and a limited role for nondisjunction or mitotic recombination (Q35165770) (← links)
- A radiation hybrid map of the distal short arm of human chromosome 11, containing the Beckwith-Wiedemann and associated embryonal tumor disease loci (Q35194082) (← links)
- Constitutional 1p36 deletion in a child with neuroblastoma. (Q35194318) (← links)
- Segregation analysis of cancer in families of childhood soft-tissue-sarcoma patients (Q35195645) (← links)
- Evidence for WT1 as a Wilms tumor (WT) gene: intragenic germinal deletion in bilateral WT (Q35196582) (← links)
- Uniparental disomy occurs infrequently in Wilms tumor patients (Q35889086) (← links)
- Tumour suppression associated with expression of human insulin-like growth factor II. (Q35984403) (← links)
- Chromosomal localisation of two putative 11p oncosuppressor genes involved in human ovarian tumours (Q35994651) (← links)
- Towards an understanding of Wilms' tumour. (Q36028194) (← links)
- Homozygous somatic Wt1 point mutations in sporadic unilateral Wilms tumor (Q36106284) (← links)
- PAX3-FOXO1 controls expression of the p57Kip2 cell-cycle regulator through degradation of EGR1. (Q36156793) (← links)
- Increasing genome instability in adrenocortical carcinoma progression with involvement of chromosomes 3, 9 and X at the adenoma stage (Q36619700) (← links)
- Adrenal incidentaloma and the Janus Kinase 2 V617F mutation: A case-based review of the literature (Q36862199) (← links)
- Progress in Top-Down Proteomics and the Analysis of Proteoforms (Q37730532) (← links)
- Candidate genes and potential targets for therapeutics in Wilms’ tumour (Q37790163) (← links)
- Polymorphisms in CARS are associated with gastric cancer risk: a two-stage case-control study in the Chinese population (Q40242627) (← links)
- Wilms' tumor: a paradigm for insights into development and cancer. (Q40456138) (← links)
- The molecular genetics of Wilms tumor: a paradigm of heterogeneity in tumor development (Q40754423) (← links)
- The molecular genetics of Wilms tumor. (Q40801112) (← links)
- Molecular genetics of Wilms' tumour (Q40941771) (← links)
- Genetics and epidemiology of Wilms' tumor: The French Wilms' tumor study (Q41084456) (← links)
- A common region of loss of heterozygosity in Wilms' tumor and embryonal rhabdomyosarcoma distal to the D11S988 locus on chromosome 11p15.5. (Q41235668) (← links)
- Suppression of the tumorigenic phenotype of a rat liver epithelial tumor cell line by the p11.2–p12 region of human chromosome 11 (Q41316754) (← links)
- Demonstration of acquired hemizygosity and clonality in acute lymphoblastic leukemia with chromosome 7 abnormalities using hypervariable DNA probes (Q43920293) (← links)
- Multiple Primary Cancers in Families With Li-Fraumeni Syndrome (Q44955059) (← links)
- Identification of a new commonly deleted region within a 2-cM interval of chromosome 11p11 in breast cancers (Q47927528) (← links)
- Homozygous inactivation of WT1 in a Wilms' tumor associated with the WAGR syndrome (Q52035238) (← links)
- Deletion of WT1 and WIT1 genes and loss of heterozygosity on chromosome 11p in Wilms tumors in Japan (Q52035521) (← links)
- Occasional loss of constitutive heterozygosity at 11p15.5 and imprinting relaxation of the IGFII maternal allele in hepatoblastoma. (Q52220644) (← links)
- Excess of multifocal tumors in nephroblastoma: implications for mechanisms of tumor development and genetic counseling. (Q53480625) (← links)
- Phenotypic severity scoring system and categorisation for prune belly syndrome: application to a pilot cohort of 50 living patients (Q57168922) (← links)
- Characterization of regions of chromosomes 12 and 16 involved in nephroblastoma tumorigenesis (Q57252309) (← links)
- Infrequent mutation of theWT1 gene in 77 Wilms' tumors (Q58298619) (← links)
- Direct pulsed field gel electrophoresis of Wilms' tumors shows that dna deletions in 11 p 13 are rare (Q58666719) (← links)
- Refinement within single yeast artificial chromosome clones of a minimal region commonly deleted on the short arm of chromosome 7 in Wilms tumours (Q58813424) (← links)
- Syndrome de Costello : aspects cliniques et risque tumoral (Q59698023) (← links)