(Q55475900)

English

Microsatellite instability and the PTEN1 gene mutation in a subset of early onset gliomas carrying germline mutation or promoter methylation of the hMLH1 gene.

scientific article published in March 2000

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scholarly article

1 reference

Europe PubMed Central

12 July 2018

http://europepmc.org/abstract/MED/10734316

Microsatellite instability and the PTEN1 gene mutation in a subset of early onset gliomas carrying germline mutation or promoter methylation of the hMLH1 gene. (English)

1 reference

Europe PubMed Central

12 July 2018

http://europepmc.org/abstract/MED/10734316

1 reference

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author name string

M Kanamori

1

1 reference

Europe PubMed Central

12 July 2018

http://europepmc.org/abstract/MED/10734316

H Kon

2

1 reference

Europe PubMed Central

12 July 2018

http://europepmc.org/abstract/MED/10734316

T Nobukuni

3

1 reference

Europe PubMed Central

12 July 2018

http://europepmc.org/abstract/MED/10734316

S Nomura

4

1 reference

Europe PubMed Central

12 July 2018

http://europepmc.org/abstract/MED/10734316

K Sugano

5

1 reference

Europe PubMed Central

12 July 2018

http://europepmc.org/abstract/MED/10734316

S Mashiyama

6

1 reference

Europe PubMed Central

12 July 2018

http://europepmc.org/abstract/MED/10734316

T Kumabe

7

1 reference

Europe PubMed Central

12 July 2018

http://europepmc.org/abstract/MED/10734316

T Yoshimoto

8

1 reference

Europe PubMed Central

12 July 2018

http://europepmc.org/abstract/MED/10734316

M Meuth

9

1 reference

Europe PubMed Central

12 July 2018

http://europepmc.org/abstract/MED/10734316

T Sekiya

10

1 reference

Europe PubMed Central

12 July 2018

http://europepmc.org/abstract/MED/10734316

Y Murakami

11

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Europe PubMed Central

12 July 2018

http://europepmc.org/abstract/MED/10734316

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publication date

1 March 2000

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Europe PubMed Central

12 July 2018

http://europepmc.org/abstract/MED/10734316

1 reference

Europe PubMed Central

12 July 2018

http://europepmc.org/abstract/MED/10734316

19

1 reference

Europe PubMed Central

12 July 2018

http://europepmc.org/abstract/MED/10734316

1564-1571

1 reference

Europe PubMed Central

12 July 2018

http://europepmc.org/abstract/MED/10734316

12

1 reference

Europe PubMed Central

12 July 2018

http://europepmc.org/abstract/MED/10734316

https://scigraph.springernature.com/pub.10.1038/sj.onc.1203454

0 references

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1 reference

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Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction

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The molecular basis of Turcot's syndrome

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Analysis of glioma cell lines for amplification and overexpression of MDM2.

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Incidence and functional consequences of hMLH1 promoter hypermethylation in colorectal carcinoma

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Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesis

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The new WHO classification of brain tumours

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Structural and functional evidence for the presence of tumor suppressor genes on the short arm of chromosome 10 in human gliomas.

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PTEN1 is frequently mutated in primary endometrial carcinomas

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Detection of amplification of a chromosomal fragment at 6p21 including the cyclin D3 gene in a glioblastoma cell line by arbitrarily primed polymerase chain reaction

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Pathways leading to glioblastoma multiforme: a molecular analysis of genetic alterations in 65 astrocytic tumors.

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Microsatellite instability and mutation of DNA mismatch repair genes in gliomas.

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PTEN, a putative protein tyrosine phosphatase gene mutated in human brain, breast, and prostate cancer

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21 January 2018

Inactivation of the type II TGF-beta receptor in colon cancer cells with microsatellite instability

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Drastic genetic instability of tumors and normal tissues in Turcot syndrome.

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Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction

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Somatic frameshift mutations in the BAX gene in colon cancers of the microsatellite mutator phenotype.

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21 January 2018

Deletion mapping of chromosome 10 in human glioma.

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Identification of a candidate tumour suppressor gene, MMAC1, at chromosome 10q23.3 that is mutated in multiple advanced cancers

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Biallelic inactivation of hMLH1 by epigenetic gene silencing, a novel mechanism causing human MSI cancers.

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Mutations of E2F-4 trinucleotide repeats in colorectal cancer with microsatellite instability

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Gene and chromosomal alterations associated with the development of human gliomas.

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Reliability of differential PCR for the detection of EGFR and MDM2 gene amplification in DNA extracted from FFPE glioma tissue.

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Novel PTEN mutations in patients with Cowden disease: absence of clear genotype-phenotype correlations

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7 January 2021

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Microsatellite instability in the insulin–like growth factor II receptor gene in gastrointestinal tumours

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7 January 2021

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Allele-specific polymerase chain reaction: a method for amplification and sequence determination of a single component among a mixture of sequence variants

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1203454

7 January 2021

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inferred from DOI database lookup

Identifiers

10.1038/SJ.ONC.1203454

1 reference

Europe PubMed Central

12 July 2018

http://europepmc.org/abstract/MED/10734316

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1 reference

Europe PubMed Central

12 July 2018

http://europepmc.org/abstract/MED/10734316

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