Lack of linkage of familial Wilms' tumour to chromosomal band 11 p13

No abstract is available for this paper.

• Publication year

  1988

• Venue

  Nature

• Publication date

  1988-11-24

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1038/336377A0PMID 2848200
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• A mitotic recombination in Wilms tumor occurs between the parathyroid hormone locus and 11p13

  2004cited by this paper
• Regional mapping of catalase and Wilms tumor—aniridia, genitourinary abnormalities, and mental retardation triad loci to the chromosome segment 11p1305→p1306

  2004cited by this paper
• High-resolution studies in patients with aniridia-Wilms tumor association

  2004cited by this paper
• Genetics of Wilms' tumor

  2004cited by this paper
• Age distribution of Wilms' tumor: report from the National Wilms' Tumor Study.

  1988cited by this paper
• Genetic mechanisms of tumor-specific loss of 11p DNA sequences in Wilms tumor.

  1987cited by this paper
• Deletion of genes on chromosome 1 in endocrine neoplasia

  1987cited by this paper
• Assignment of multiple endocrine neoplasia type 2A to chromosome 10 by linkage

  1987cited by this paper
• A linked genetic marker for multiple endocrine neoplasia type 2A on chromosome 10

  1987cited by this paper
• DNA Sequence and Regional Assignment of the Human Follicle-Stimulating Hormone β-Subunit Gene to the Short Arm of Human Chromosome 11

  1987cited by this paper
• An EcoRI polymorphism associated with a human genomic clone from band 11p13.

  1987cited by this paper
• The anonymous RFLP locus D11S16 is tightly linked to catalase on 11p.

  1987cited by this paper
• Loss of heterozygosity in three embryonal tumours suggests a common pathogenetic mechanism

  1985cited by this paper
• Analysis of Human Genetic Linkage

  1985cited by this paper
• A systematic approach for detecting high-frequency restriction fragment length polymorphisms using large genomic probes.

  1985cited by this paper
• Development of homozygosity for chromosome 11p markers in Wilms' tumour

  1984cited by this paper
• Loss of alleles at loci on human chromosome 11 during genesis of Wilms' tumour

  1984cited by this paper
• Somatic deletion and duplication of genes on chromosome 11 in Wilms' tumours

  1984cited by this paper
• Loss of a Harvey ras allele in sporadic Wilms' tumour

  1984cited by this paper
• Chromosome number 11 and Wilms' tumor.

  1982cited by this paper
• Isolation of a transforming sequence from a human bladder carcinoma cell line.

  1982cited by this paper
• Nucleotide sequence of cloned cDNAs encoding human preproparathyroid hormone.

  1981cited by this paper
• Interstitial deletion of short arm of chromosome 11 limited to Wilms' tumor cells in a patient without aniridia.

  1981cited by this paper
• Polymorphic DNA region adjacent to the 5' end of the human insulin gene.

  1981cited by this paper
• Aniridia-Wilms tumor association.

  1981cited by this paper
• Familial occurrence of the aniridia-Wilms tumor syndrome with deletion 11p13-14.1.

  1980cited by this paper
• Clinical Pediatric Oncology

  1978cited by this paper
• Chromosomal imbalance in the Aniridia-Wilms' tumor association: 11p interstitial deletion.

  1978cited by this paper
• Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies.

  1974cited by this paper

• The potential role of immunotherapy in Wilms' tumor: opportunities and challenges.

  2023cites this paper
• Hallmark discoveries in the biology of Wilms tumour

  2023cites this paper
• Recent advances in Wilms tumor predisposition.

  2020cites this paper
• Convergent evolution of 11p allelic loss in multifocal Wilms tumors arising in WT1 mutation carriers

  2018cites this paper
• Wilms Tumor Overview

  2013cites this paper
• Maligne Erkrankungen bei Kindern und Jugendlichen nach in-vitro Fertilisation

  2012cites this paper
• Pathology, genetics and cytogenetics of Wilms' tumour

  2011cites this paper
• Characterisation in mice of a conserved sequence, Mcr2, associated with the Wilms' tumour 1 (Wt1) locus

  2010cites this paper
• Cas familiaux de néphroblastomes et de neuroblastomes

  2009cites this paper
• An immunohistochemical and microsatellite analysis of nephroblastomas.

  2008cites this paper
• Advances in Brief Evidence for the Involvement of a Potential Second Tumor Suppressor Gene on Chromosome 17 Distinct from p 53 in Malignant Astrocytomas

  2007cites this paper
• Familial extrarenal Wilms tumor.

  2007cites this paper
• Angelman Syndrome: Three Molecular Classes Identified with Chromosome I SqII qI 3-specific DNA Markers

  2006cites this paper
• Chromosome 11 Putative Tumor Suppressor Regions , Is Limited to Loss of Heterozygosity in Wilms ' Tumors , Studied for Six Updated

  2006cites this paper
• Wilms' tumor: starting off the kidney all over again?

  2005cites this paper
• Nephroblastom — Wilms-Tumor

  2005cites this paper
• Nephroblastic neoplasms.

  2005cites this paper
• Familial Wilms tumor

  2004cites this paper
• Tumor-Suppressor Genes

  2003cites this paper
• The two‐hit model for Wilms' tumor: Where are we 30 years later?

  2003cites this paper
• Molecular genetic analysis of non-familial renal cell carcinoma.

  2002cites this paper
• Consistent Loss of the D 5 S 89 Locus Mapping Telomeric to the Interleukin Gene Cluster and Centromeric to EGR-1 in Patients With 5 q-Chromosome

  2002cites this paper
• Recent advances in Wilms tumor genetics

  2002cites this paper
• Principles of Wilms' tumor biology.

  2000cites this paper
• Familial Wilms' Tumor with Neural Elements: Characterization by Histology, Immunohistochemistry, and Genetic Analysis

  2000cites this paper
• Evidence for susceptibility genes to familial Wilms tumour in addition to WT1, FWT1 and FWT2

  2000cites this paper
• Wilmstumor- und Metanephrogenese: Differenzielle Genexpressionsanalysen und weitere Charakterisierung identifizierter Kandidatengene

  2000cites this paper
• High frequency of loss of heterozygosity for 1p35-p36 (D1S247) in Wilms tumor.

  2000cites this paper
• Correlation of chromosome abnormalities with presence or absence of WT1 deletions/mutations in Wilms tumor

  1999cites this paper
• Genetics of Wilms' tumor.

  1999cites this paper
• Bilateral Wilms' tumor: a clinicopathologic review.

  1999cites this paper
• Summary PAX 8 , a human paired box gene : isolation and expression in developing thyroid , kidney and Wilms ’ tumors

  1999cites this paper
• Isochromosomes 7q and 17q in Wilms tumor.

  1998cites this paper
• The approach to common abdominal diagnosis in infants and children.

  1998cites this paper
• The approach to common abdominal diagnoses in infants and children. Part II.

  1998cites this paper
• Constitutional WT1 mutations in Wilms' tumor patients.

  1998cites this paper
• Wilms tumor genetics.

  1998cites this paper
• Linkage of familial Wilms' tumor predisposition to chromosome 19 and a two-locus model for the etiology of familial tumors.

  1998cites this paper
• Confirmation of FWT1 as a Wilms’ tumour susceptibility gene and phenotypic characteristics of Wilms’ tumour attributable to FWT1

  1998cites this paper
• Loss of heterozygosity for the short arm of chromosome 7 in sporadic Wilms tumour

  1998cites this paper
• Molecular and surgical advances in pediatric tumors.

  1997cites this paper
• Correlation of germ-line mutations and two-hit inactivation of the WT1 gene with Wilms tumors of stromal-predominant histology.

  1997cites this paper
• Evidence for genetic heterogeneity in familial Wilms' tumor.

  1997cites this paper
• Molecular basis of Wilms' tumor.

  1997cites this paper
• A clinical overview of WT1 gene mutations

  1997cites this paper
• The familial Wilms' tumour susceptibility gene, FWT1, may not be a tumour suppressor gene

  1997cites this paper
• [Genetic alterations associated with pathologic differentiation of Wilms' tumors].

  1997cites this paper
• Progress of fundamental research in Wilms' tumor

  1997cites this paper
• Genetics of renal tumours

  1997cites this paper
• Chromosomal Aberrations in Wilms' Tumour

  1997cites this paper
• Wilms' tumour.

  1997cites this paper
• Tumor suppressor genes and human cancer.

  1997cites this paper
• Familial Wilms' tumor: a descriptive study.

  1996cites this paper
• The ABL genes in normal and abnormal cell development.

  1996cites this paper
• +P5 (D1S3309E), a novel target binding site for the Wilms' tumour suppressor 1 (WT1) gene, maps to human chromosome 1q21-->22.

  1996cites this paper
• Genetische Grundlagen hereditärer urologischer Erkrankungen

  1996cites this paper
• Evidence for a familial Wilms' tumour gene (FWT1) on chromosome 17q12–q21

  1996cites this paper
• Familial predisposition to neuroblastoma does not map to chromosome band 1p36.

  1996cites this paper
• Identification of novel regions of deletion in familial Wilms' tumor by comparative genomic hybridization.

  1996cites this paper
• Role of genomic imprinting in Wilms' tumour and overgrowth disorders.

  1996cites this paper
• Genetic epidemiology of childhood cancer.

  1996cites this paper
• The Molecular Genetics of Wilms Tumor

  1996cites this paper
• Wilms tumour and other genetic causes of renal cancer

  1996cites this paper
• An overview of the clinical and molecular genetics of Wilms' tumor.

  1996cites this paper
• A common region of loss of heterozygosity in Wilms' tumor and embryonal rhabdomyosarcoma distal to the D11S988 locus on chromosome 11p15.5

  1996cites this paper
• Familial Wilms' tumor associated with a WT1 zinc finger mutation.

  1996cites this paper
• Wilms tumor

  1996cites this paper
• Involvement of chromosome 7 in Wilms tumor.

  1995cites this paper
• Molecular genetics of Wilms' tumour

  1995cites this paper
• WT1 exon 1 deletion/insertion mutations in Wilms tumor patients, associated with di- and trinucleotide repeats and deletion hotspot consensus sequences.

  1995cites this paper
• Wilms tumor: to cure and understanding.

  1995cites this paper
• Characterization of regions of chromosomes 12 and 16 involved in nephroblastoma tumorigenesis

  1995cites this paper
• Molecular advances in pediatric urology.

  1995cites this paper
• Molecular genetics of Wilms tumor.

  1995cites this paper
• Expression and structure of hox genes in wilms-tumor.

  1995cites this paper
• Etiology of Wilms' tumor.

  1995cites this paper
• Other Loci Implicated in Wilms Tumor

  1995cites this paper
• Genomic imprinting and cancer.

  1995cites this paper
• Allelotyping in Wilms tumors identifies a putative third tumor suppressor gene on chromosome 11.

  1995cites this paper
• Wilms' tumor: a paradigm for insights into development and cancer.

  1995cites this paper
• Genome-wide loss of maternal alleles in a nephrogenic rest and Wilms' tumour from a BWS patient

  1995cites this paper
• Genetics of embryonal tumours of childhood: retinoblastoma, Wilms' tumour and neuroblastoma.

  1995cites this paper
• Non-11p constitutional chromosome abnormalities in Wilms' tumor patients.

  1995cites this paper
• Epidemiologic features of Wilms tumor.

  1995cites this paper
• Genetics of paediatric solid tumours.

  1994cites this paper
• Proto-oncogenes and tumor suppressor genes in human urological malignancies.

  1994cites this paper
• Concordance between parental origin of chromosome 13q loss and chromosome 6p duplication in sporadic retinoblastoma.

  1994cites this paper
• Paired box mutations in familial and sporadic aniridia predicts truncated aniridia proteins.

  1994cites this paper
• Testicular germ cell tumors of adults show deletions of chromosomal bands 11 p13 and 11p15.5, but no abnormalities within the zinc‐finger regions and exons 2 and 6 of the wilms' Tumor 1 Gene

  1994cites this paper
• Contribution of MAV-1-induced nephroblastoma to the study of genes involved in human Wilms' tumor development.

  1994cites this paper
• Genetic epidemiology of cancer: A multidisciplinary approach

  1994cites this paper
• The management and biological behavior of Wilms tumor.

  1994cites this paper
• Molecular Biology and Genetic Advances in Childhood Malignancies

  1994cites this paper
• Genetic Factors in Solid Tumors of Childhood

  1994cites this paper
• The molecular genetics of Wilms tumor.

  1994cites this paper
• Molecular genetic analysis of chromosome 11p in familial Wilms tumour.

  1994cites this paper
• Consistent loss of the D5S89 locus mapping telomeric to the interleukin gene cluster and centromeric to EGR-1 in patients with 5q- chromosome.

  1994cites this paper
• Germline and somatic abnormalities of chromosome 7 in Wilms' tumor.

  1994cites this paper
• Tumor suppressor genes in molecular medicine

  1994cites this paper
• Genetic events in the development of Wilms' tumor.

  1994cites this paper