(Q48180185)

English

Loss of heterozygosity and the origin of meningioma.

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scholarly article

1 reference

Europe PubMed Central

9 February 2018

http://europepmc.org/abstract/MED/2891603

Loss of heterozygosity and the origin of meningioma. (English)

1 reference

Europe PubMed Central

9 February 2018

http://europepmc.org/abstract/MED/2891603

1 reference

based on heuristic

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author name string

E Meese

1

1 reference

Europe PubMed Central

9 February 2018

http://europepmc.org/abstract/MED/2891603

N Blin

2

1 reference

Europe PubMed Central

9 February 2018

http://europepmc.org/abstract/MED/2891603

K D Zang

3

1 reference

Europe PubMed Central

9 February 2018

http://europepmc.org/abstract/MED/2891603

publication date

1 December 1987

1 reference

Europe PubMed Central

9 February 2018

http://europepmc.org/abstract/MED/2891603

1 reference

Europe PubMed Central

9 February 2018

http://europepmc.org/abstract/MED/2891603

77

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Europe PubMed Central

9 February 2018

http://europepmc.org/abstract/MED/2891603

349-351

1 reference

Europe PubMed Central

9 February 2018

http://europepmc.org/abstract/MED/2891603

4

1 reference

Europe PubMed Central

9 February 2018

http://europepmc.org/abstract/MED/2891603

https://scigraph.springernature.com/pub.10.1007/bf00291425

0 references

An anonymous single copy chromosome 22 clone, D22S10 (22c1-18) identifies an RFLP with PstI.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2891603

12 December 2020

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Enhanced expression of four cellular oncogenes in a human glioblastoma cell line

1 reference

https://pubmed.ncbi.nlm.nih.gov/2891603

12 December 2020

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Human breast cancer: correlation of relapse and survival with amplification of the HER-2/neu oncogene

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https://pubmed.ncbi.nlm.nih.gov/2891603

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Model Hereditary Cancers of Man

1 reference

https://pubmed.ncbi.nlm.nih.gov/2891603

12 December 2020

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2891603

12 December 2020

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Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/2891603

12 December 2020

based on heuristic

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Chromosomal Constitution of Meningiomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/2891603

12 December 2020

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Osteosarcoma and retinoblastoma: a shared chromosomal mechanism revealing recessive predisposition

1 reference

https://pubmed.ncbi.nlm.nih.gov/2891603

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A general theory of carcinogenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/2891603

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2891603

12 December 2020

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Loss of a Harvey ras allele in sporadic Wilms' tumour

1 reference

https://pubmed.ncbi.nlm.nih.gov/2891603

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Loss of alleles at loci on human chromosome 11 during genesis of Wilms' tumour

1 reference

https://pubmed.ncbi.nlm.nih.gov/2891603

12 December 2020

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inferred from PubMed ID database lookup

Genetic implication of karyological instability of malignant somatic cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/2891603

12 December 2020

based on heuristic

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Association of multiple copies of the N-myc oncogene with rapid progression of neuroblastomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/2891603

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Loss of heterozygosity in three embryonal tumours suggests a common pathogenetic mechanism

1 reference

https://pubmed.ncbi.nlm.nih.gov/2891603

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An estimate of unique DNA sequence heterozygosity in the human genome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2891603

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2891603

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Patient with 13 Chromosome Deletion: Evidence That the Retinoblastoma Gene Is a Recessive Cancer Gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/2891603

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human chromosome 22.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2891603

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00291425

1 reference

Europe PubMed Central

9 February 2018

http://europepmc.org/abstract/MED/2891603

1 reference

Europe PubMed Central

9 February 2018

http://europepmc.org/abstract/MED/2891603

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