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Literature DB >> 6288229

Cytological and cytogenetical studies on human meningioma.

K D Zang.

Abstract

Entities: Disease Species

Mesh：

Substances：
DNA, Viral

Year: 1982 PMID： 6288229 DOI： 10.1016/0165-4608(82)90063-2

Source DB: PubMed Journal: Cancer Genet Cytogenet ISSN： 0165-4608

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Cited

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38 in total

Review 1. Molecular genetics of neurological tumours.

Authors: R Y Chung; B R Seizinger
Journal: J Med Genet Date: 1992-06 Impact factor: 6.318

2. Maternally expressed gene 3, an imprinted noncoding RNA gene, is associated with meningioma pathogenesis and progression.

Authors: Xun Zhang; Roger Gejman; Ali Mahta; Ying Zhong; Kimberley A Rice; Yunli Zhou; Pornsuk Cheunsuchon; David N Louis; Anne Klibanski
Journal: Cancer Res Date: 2010-02-23 Impact factor: 12.701

3. Identification of twelve new RFLP-markers on chromosome 22q11-qter.

Authors: E Carlbom; N Sugawa; C Larsson; P J Scambler; J P Dumanski; V P Collins; M Nordenskjöld
Journal: Hum Genet Date: 1991-12 Impact factor: 4.132

4. Hyperdiploidy defines a distinct cytogenetic entity of meningiomas.

Authors: Ralf Ketter; Yoo-Jin Kim; Simone Storck; Jörg Rahnenführer; Bernd F M Romeike; Wolf-Ingo Steudel; Klaus D Zang; Wolfram Henn
Journal: J Neurooncol Date: 2007-01-17 Impact factor: 4.130

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

Authors: W Krone; I Högemann
Journal: Hum Genet Date: 1986-12 Impact factor: 4.132

Cytological and cytogenetical studies on human meningioma.

Review 1. Molecular genetics of neurological tumours.

2. Maternally expressed gene 3, an imprinted noncoding RNA gene, is associated with meningioma pathogenesis and progression.

3. Identification of twelve new RFLP-markers on chromosome 22q11-qter.

4. Hyperdiploidy defines a distinct cytogenetic entity of meningiomas.

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

6. Expression patterns of the p53 tumor suppressor gene and the mdm2 proto-oncogene in human meningiomas.

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

8. Loss of heterozygosity on chromosome 22q and 17p correlates with aggressiveness of meningiomas.

9. Cellular schwannoma. A clinicopathologic study of 29 cases.

10. On six cases of radiation meningiomas from the same community.