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Literature DB >> 2883892

Nonrandom loss of maternal chromosome 11 alleles in Wilms tumors.

W T Schroeder, L Y Chao, D D Dao, L C Strong, S Pathak, V Riccardi, W H Lewis, G F Saunders.

Abstract

A series of gene probes for chromosome 11 has been used to study the genetic events associated with the development of Wilms tumor. Examination of DNA samples from five patients with Wilms tumor in whom the tumors showed loss of chromosome 11 alleles and their parents indicate that alleles lost in the tumors are of maternal origin. These data suggest that the parental derivation of chromosome 11 alleles lost in these Wilms tumors is not random.

Entities: Disease Species

Mesh：

Substances：

Year: 1987 PMID： 2883892 PMCID： PMC1684136

Source DB: PubMed Journal: Am J Hum Genet ISSN： 0002-9297 Impact factor: 11.025

24 in total

1. Prognosis and treatment of Wilms' tumor at Great Ormond Street Hospital for Sick Children--1960-1972.

Authors: J V Bond
Journal: Cancer Date: 1975-10 Impact factor: 6.860

2. Chromosomal imbalance in the Aniridia-Wilms' tumor association: 11p interstitial deletion.

Authors: V M Riccardi; E Sujansky; A C Smith; U Francke
Journal: Pediatrics Date: 1978-04 Impact factor: 7.124

3. Mutation and cancer: a model for Wilms' tumor of the kidney.

Authors: A G Knudson; L C Strong
Journal: J Natl Cancer Inst Date: 1972-02 Impact factor: 13.506

4. Polymorphic DNA region adjacent to the 5' end of the human insulin gene.

Authors: G I Bell; J H Karam; W J Rutter
Journal: Proc Natl Acad Sci U S A Date: 1981-09 Impact factor: 11.205

5. Nucleotide sequence of cloned cDNAs encoding human preproparathyroid hormone.

Authors: G N Hendy; H M Kronenberg; J T Potts; A Rich
Journal: Proc Natl Acad Sci U S A Date: 1981-12 Impact factor: 11.205

6. Localization of the human insulin gene to the distal end of the short arm of chromosome 11.

Authors: M E Harper; A Ullrich; G F Saunders
Journal: Proc Natl Acad Sci U S A Date: 1981-07 Impact factor: 11.205

7. Occupations of fathers of patients with Wilms's tumour.

Authors: A F Kantor; M G Curnen; J W Meigs; J T Flannery
Journal: J Epidemiol Community Health Date: 1979-12 Impact factor: 3.710

8. Fetal rhabdomyomatous nephroblastoma-a variant of Wilms' tumor.

Authors: H J Wigger
Journal: Hum Pathol Date: 1976-11 Impact factor: 3.466

9. Rhabdomyogenesis in renal neoplasia of childhood.

Authors: F Gonzalez-Crussi; W Hsueh; N Ugarte
Journal: Am J Surg Pathol Date: 1981-09 Impact factor: 6.394

10. The Drash syndrome: male pseudohermaphroditism, nephritis, and Wilms tumor.

Authors: S M Goldman; D J Garfinkel; K S Oh; J P Dorst
Journal: Radiology Date: 1981-10 Impact factor: 11.105

49 in total

1. The aetiology of cancer in the very young.

Authors: J D Buckley
Journal: Br J Cancer Suppl Date: 1992-08

Review 2. Genomic imprinting.

Authors: J G Hall
Journal: Arch Dis Child Date: 1990-10 Impact factor: 3.791

Nonrandom loss of maternal chromosome 11 alleles in Wilms tumors.

1. Prognosis and treatment of Wilms' tumor at Great Ormond Street Hospital for Sick Children--1960-1972.

2. Chromosomal imbalance in the Aniridia-Wilms' tumor association: 11p interstitial deletion.

3. Mutation and cancer: a model for Wilms' tumor of the kidney.

4. Polymorphic DNA region adjacent to the 5' end of the human insulin gene.

5. Nucleotide sequence of cloned cDNAs encoding human preproparathyroid hormone.

6. Localization of the human insulin gene to the distal end of the short arm of chromosome 11.

7. Occupations of fathers of patients with Wilms's tumour.

8. Fetal rhabdomyomatous nephroblastoma-a variant of Wilms' tumor.

9. Rhabdomyogenesis in renal neoplasia of childhood.

10. The Drash syndrome: male pseudohermaphroditism, nephritis, and Wilms tumor.

1. The aetiology of cancer in the very young.

Review 2. Genomic imprinting.

Review 3. Candidate genes and potential targets for therapeutics in Wilms' tumour.

4. Embryonal tumours and genomic imprinting.

5. Parental age and childhood cancer risk: A Danish population-based registry study.

Review 6. Wilms' tumour: a complex enigma to decipher.

7. Parental origin of chromosome 22 alleles lost in meningioma.

8. Concordance between parental origin of chromosome 13q loss and chromosome 6p duplication in sporadic retinoblastoma.

9. Uniparental disomy occurs infrequently in Wilms tumor patients.

10. Parental bias of Ki-ras oncogenes detected in lung tumors from mouse hybrids.