Literature DB >> 3098672

Cell culture studies on neurofibromatosis (von Recklinghausen). V. Monosomy 22 and other chromosomal anomalies in cultures from peripheral neurofibromas.

W Krone, I Högemann.   

Abstract

Cell cultures grown from peripheral neurofibromas of three patients suffering from sporadic peripheral neurofibromatosis (NF) were analysed cytogenetically at early in vitro passages. The NF-cultures exhibited a 6.7-fold higher frequency of aneuploid mitoses, including pseudodiploids, than the control cultures derived from the skin of three healthy donors. The predominant numerical anomaly was monosomy 22. Several, as yet unidentified marker chromosomes occurred in the NF-cultures, which also showed a much higher level of unstable chromosomal anomalies. The role of monosomy 22 in tumorigenesis of meningiomas and neurofibromas is discussed.

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Year:  1986        PMID: 3098672     DOI: 10.1007/bf00280506

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  22 in total

1.  Loss of genes on chromosome 22 in tumorigenesis of human acoustic neuroma.

Authors:  B R Seizinger; R L Martuza; J F Gusella
Journal:  Nature       Date:  1986 Aug 14-20       Impact factor: 49.962

2.  Cytological and cytogenetical studies on brain tumors. 3. Ph1-like chromosomes in human meningiomas.

Authors:  H Zankl; K D Zang
Journal:  Humangenetik       Date:  1971

3.  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

4.  Neurofibromatosis: no chromosomal defect by prophase banding technique.

Authors:  Y S Kao; C S Kao-Shan; T Knutsen; J Whang-Peng; J J Mulvihill
Journal:  Cancer Genet Cytogenet       Date:  1984-11

5.  The beta-subunit of follicle-stimulating hormone is deleted in patients with aniridia and Wilms' tumour, allowing a further definition of the WAGR locus.

Authors:  T Glaser; W H Lewis; G A Bruns; P C Watkins; C E Rogler; T B Shows; V E Powers; H F Willard; J M Goguen; K O Simola
Journal:  Nature       Date:  1986 Jun 26-Jul 2       Impact factor: 49.962

6.  Development of homozygosity for chromosome 11p markers in Wilms' tumour.

Authors:  S H Orkin; D S Goldman; S E Sallan
Journal:  Nature       Date:  1984 May 10-16       Impact factor: 49.962

7.  Multiple meningiomas diagnosed by computed tomography.

Authors:  F Federico; P D'Aprile; A Lorusso; M Belsanti; A Carella
Journal:  Ital J Neurol Sci       Date:  1984-09

8.  A general theory of carcinogenesis.

Authors:  D E Comings
Journal:  Proc Natl Acad Sci U S A       Date:  1973-12       Impact factor: 11.205

9.  The cytogenetics of Wilms' tumor.

Authors:  R M Slater
Journal:  Cancer Genet Cytogenet       Date:  1986-01-01

10.  Cell culture studies on neurofibromatosis (von Recklinghausen). II. Occurrence of glial cells in primary cultures of peripheral neurofibromas.

Authors:  W Krone; G Jirikowski; O Mühleck; H Kling; H Gall
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

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  4 in total

1.  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

2.  Chromosomes 17 and 22 involved in marker formation in neurofibrosarcoma in von Recklinghausen disease. A cytogenetic and in situ hybridization study.

Authors:  H J Decker; L A Cannizzaro; M J Mendez; S P Leong; H Bixenman; C Berger; A A Sandberg
Journal:  Hum Genet       Date:  1990-08       Impact factor: 4.132

Review 3.  Malignant Peripheral Nerve Sheath Tumors: From Epigenome to Bedside.

Authors:  Justin Korfhage; David B Lombard
Journal:  Mol Cancer Res       Date:  2019-04-25       Impact factor: 5.852

4.  DNA linkage analysis in Von Recklinghausen neurofibromatosis.

Authors:  B R Seizinger; G Rouleau; A H Lane; L J Ozelius; A G Faryniarz; J Iannazzi; W Hobbs; J C Roy; B Falcone; S Huson
Journal:  J Med Genet       Date:  1987-09       Impact factor: 6.318

  4 in total

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