Literature DB >> 3712397

Multifocal meningiomas in a patient with a constitutional ring chromosome 22.

T Arinami, I Kondo, H Hamaguchi, S Nakajima.   

Abstract

We report a patient with a constitutional ring chromosome 22, in whom multifocal meningiomas were confirmed at necropsy, and discuss the relationship between the constitutional chromosome change and tumourigenesis of meningiomas in this patient.

Entities:  

Mesh:

Year:  1986        PMID: 3712397      PMCID: PMC1049578          DOI: 10.1136/jmg.23.2.178

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  5 in total

1.  Cytological and cytogenetical studies on brain tumors. 4. Identification of the missing G chromosome in human meningiomas as no. 22 by fluorescence technique.

Authors:  H Zankl; K D Zang
Journal:  Humangenetik       Date:  1972

2.  Expression of recessive alleles by chromosomal mechanisms in retinoblastoma.

Authors:  W K Cavenee; T P Dryja; R A Phillips; W F Benedict; R Godbout; B L Gallie; A L Murphree; L C Strong; R L White
Journal:  Nature       Date:  1983 Oct 27-Nov 2       Impact factor: 49.962

3.  Segregation of a 22 ring chromosome in three generations.

Authors:  C Stoll; M P Roth
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

4.  Chromosomal mapping of the simian sarcoma virus onc gene analogue in human cells.

Authors:  D C Swan; O W McBride; K C Robbins; D A Keithley; E P Reddy; S A Aaronson
Journal:  Proc Natl Acad Sci U S A       Date:  1982-08       Impact factor: 11.205

5.  A cytogenetic survey of 449 patients in a Japanese institution for the mentally retarded.

Authors:  I Kondo; H Hamaguchi; S Nakajima; T Haneda
Journal:  Clin Genet       Date:  1980       Impact factor: 4.438

  5 in total
  11 in total

1.  Screening for mutations in the neurofibromatosis type 2 (NF2) gene in sporadic meningiomas.

Authors:  L R De Vitis; A Tedde; F Vitelli; F Ammannati; P Mennonna; U Bigozzi; E Montali; L Papi
Journal:  Hum Genet       Date:  1996-05       Impact factor: 4.132

2.  Cytogenetic and in situ DNA-hybridization studies in intracranial tumors of a patient with central neurofibromatosis.

Authors:  B Wullich; M Kiechle-Schwarz; L Mayfrank; W Schempp
Journal:  Hum Genet       Date:  1989-04       Impact factor: 4.132

Review 3.  Human chromosome 22.

Authors:  J C Kaplan; A Aurias; C Julier; M Prieur; M F Szajnert
Journal:  J Med Genet       Date:  1987-02       Impact factor: 6.318

Review 4.  Constitutional ring chromosomes and tumour suppressor genes.

Authors:  N Tommerup; R Lothe
Journal:  J Med Genet       Date:  1992-12       Impact factor: 6.318

5.  Molecular studies of DiGeorge syndrome.

Authors:  W J Fibison; M Budarf; H McDermid; F Greenberg; B S Emanuel
Journal:  Am J Hum Genet       Date:  1990-05       Impact factor: 11.025

6.  Metachromatic leucodystrophy (MLD) in a patient with a constitutional ring chromosome 22.

Authors:  M B Coulter-Mackie; J Rip; M D Ludman; J Beis; D E Cole
Journal:  J Med Genet       Date:  1995-10       Impact factor: 6.318

7.  Deletion mapping of a locus on human chromosome 22 involved in the oncogenesis of meningioma.

Authors:  J P Dumanski; E Carlbom; V P Collins; M Nordenskjöld
Journal:  Proc Natl Acad Sci U S A       Date:  1987-12       Impact factor: 11.205

8.  Comprehensive genetic and epigenetic analysis of sporadic meningioma for macro-mutations on 22q and micro-mutations within the NF2 locus.

Authors:  Caisa M Hansson; Patrick G Buckley; Giedre Grigelioniene; Arkadiusz Piotrowski; Anders R Hellström; Kiran Mantripragada; Caroline Jarbo; Tiit Mathiesen; Jan P Dumanski
Journal:  BMC Genomics       Date:  2007-01-12       Impact factor: 3.969

Review 9.  The ninth Gordon Hamilton-Fairley memorial lecture. Hereditary cancers: clues to mechanisms of carcinogenesis.

Authors:  A G Knudson
Journal:  Br J Cancer       Date:  1989-05       Impact factor: 7.640

10.  Pathogenesis of vestibular schwannoma in ring chromosome 22.

Authors:  Ellen Denayer; Hilde Brems; Paul de Cock; Gareth D Evans; Frank Van Calenbergh; Naomi Bowers; Raf Sciot; Maria Debiec-Rychter; Joris V Vermeesch; Jean-Pierre Fryns; Eric Legius
Journal:  BMC Med Genet       Date:  2009-09-22       Impact factor: 2.103

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