(Q34723085)

4 August 2017

1 reference

title

Microsatellite instability and its relevance to cutaneous tumorigenesis (English)

1 reference

4 August 2017

1 reference

Mahmoud R Hussein

1

1 reference

PubMed ID

12100625

4 August 2017

Gary S Wood

series ordinal

2

1 reference

4 August 2017

1 May 2002

1 reference

Journal of Cutaneous Pathology

4 August 2017

1 reference

4 August 2017

29

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4 August 2017

257-267

1 reference

4 August 2017

5

1 reference

Clues to the pathogenesis of familial colorectal cancer

4 August 2017

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Microsatellite instability differences between familial and sporadic ovarian cancers

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Mutation of human short tandem repeats

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Enhanced Gene Expression by the Poly(dT-dG) · Poly(dC-dA) Sequence

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Human fetal G gamma- and A gamma-globin genes: complete nucleotide sequences suggest that DNA can be exchanged between these duplicated genes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Eukaryotic topoisomerase II preferentially cleaves alternating purine-pyrimidine repeats

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Microsatellite polymorphism linkage map of human chromosome 13q.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Microsatellite instability in cancer of the proximal colon

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Genetic mapping of a locus predisposing to human colorectal cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

High frequencies of short frameshifts in poly-CA/TG tandem repeats borne by bacteriophage M13 in Escherichia coli K-12.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Genomic instability in repeated sequences is an early somatic event in colorectal tumorigenesis that persists after transformation

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Mismatch repair defects in human carcinogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

DNA chaperones: a solution to a persistence problem?

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Genetic and antigenic characterization of a serotype G6 human rotavirus isolated in Melbourne, Australia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

GTBP, a 160-kilodalton protein essential for mismatch-binding activity in human cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Genetic instability occurs in the majority of young patients with colorectal cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Microsatellite alterations as clonal markers for the detection of human cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Expression of five selected human mismatch repair genes simultaneously detected in normal and cancer cell lines by a nonradioactive multiplex reverse transcription-polymerase chain reaction

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Spontaneous mutation rates to new length alleles at tandem-repetitive hypervariable loci in human DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

A second-generation linkage map of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Instability of short tandem repeats (microsatellites) in human cancers.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Tumor suppressors: recessive mutations that lead to cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Mutations of two PMS homologues in hereditary nonpolyposis colon cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

DNA-replication fidelity, mismatch repair and genome instability in cancer cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Mutational analysis of mismatch repair genes, hMLH1 and hMSH2, in sporadic endometrial carcinomas with microsatellite instability

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Sporadic gastric carcinomas with microsatellite instability display a particular clinicopathologic profile.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Isolation of an hMSH2-p160 heterodimer that restores DNA mismatch repair to tumor cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Mutations of GTBP in genetically unstable cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Microsatellite instability in childhood rhabdomyosarcoma is locus specific and correlates with fractional allelic loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Mutation of a mutL homolog in hereditary colon cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

hMSH2 forms specific mispair-binding complexes with hMSH3 and hMSH6

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Mutation of hMSH3 and hMSH6 mismatch repair genes in genetically unstable human colorectal and gastric carcinomas

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

MLH1 promoter hypermethylation is associated with the microsatellite instability phenotype in sporadic endometrial carcinomas

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Incidence and functional consequences of hMLH1 promoter hypermethylation in colorectal carcinoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Characterisation of a subtype of colorectal cancer combining features of the suppressor and mild mutator pathways

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Morphology of sporadic colorectal cancer with DNA replication errors

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Molecular nature of colon tumors in hereditary nonpolyposis colon cancer, familial polyposis, and sporadic colon cancer.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Mutations at coding mononucleotide repeats in gastric cancer with the microsatellite mutator phenotype.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

The clinicopathological features of gastric carcinomas with microsatellite instability may be mediated by mutations of different "target genes": a study of the TGFbeta RII, IGFII R, and BAX genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Molecular screening. Prospects for a new approach

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Frameshift mutations and the genetic code. This paper is dedicated to Professor Theodosius Dobzhansky on the occasion of his 66th birthday

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Preferential DNA secondary structure mutagenesis in the lagging strand of replication in E. coli

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Biological asymmetries and the fidelity of eukaryotic DNA replication

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Evolution of Repeated DNA Sequences by Unequal Crossover

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Microsatellite instability: the mutator that mutates the other mutator

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Mismatch repair deficiency in phenotypically normal human cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Inactivation of the mouse Msh2 gene results in mismatch repair deficiency, methylation tolerance, hyperrecombination, and predisposition to cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

A case of multiple sebaceous epithelioma: analysis of microsatellite instability

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Colorectal cancer and the Muir-Torre syndrome in a Gypsy family: a review

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Muir-Torre syndrome: case report of a patient with concurrent jejunal and ureteral cancer and a review of the literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Muir-Torre phenotype has a frequency of DNA mismatch-repair-gene mutations similar to that in hereditary nonpolyposis colorectal cancer families defined by the Amsterdam criteria

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Rarity of genomic instability in pathogenesis of systemic anaplastic large cell lymphoma (ALCL) in immunocompetent patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Microsatellite instability in human non-melanoma and melanoma skin cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Microsatellite instability and loss of heterozygosity in melanoma.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Definition of the role of chromosome 9p21 in sporadic melanoma through genetic analysis of primary tumours and their metastases. The Melanoma Cooperative Group.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

High frequency of loss of heterozygosity on chromosome region 9p21-p22 but lack of p16INK4a/p19ARF mutations in greek patients with basal cell carcinoma of the skin

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Allele loss on chromosome 11q and microsatellite instability in malignant melanoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Loss of the wild type MLH1 gene is a feature of hereditary nonpolyposis colorectal cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Analysis of mismatch repair genes in hereditary non–polyposis colorectal cancer patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Microsatellite Instability in Benign Skin Lesions in Hereditary Non-Polyposis Colorectal Cancer Syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Molecular Pathologic Analysis Enhances the Diagnosis and Management of Muir-Torre Syndrome and Gives Insight Into Its Underlying Molecular Pathogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Erratum: Destabilization of tracts of simple repetitive DNA in yeast by mutations affecting DNA mismatch repair

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Genetic mapping of a second locus predisposing to hereditary non–polyposis colon cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Complex gene conversion events in germline mutation at human minisatellites

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

Informativeness of human (dC-dA)n.(dG-dT)n polymorphisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

7 January 2021

Detection of microsatellite alterations in the spectrum of melanocytic nevi in patients with or without individual or family history of melanoma

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

7 January 2021

Roles of the DNA mismatch repair genes in colorectal tumorigenesis

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

7 January 2021

Detection of bladder cancer recurrence by microsatellite analysis of urine

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

7 January 2021

Microsatellite instability in primary and metastatic melanoma

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

7 January 2021

Comprehensive analysis of 112 melanocytic skin lesions demonstrates microsatellite instability in melanomas and dysplastic nevi, but not in benign nevi

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

7 January 2021

Microsatellite instability and alterations in the hMSH2 gene in human ovarian cancer

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

7 January 2021

The yeast gene MSH3 defines a new class of eukaryotic MutS homologues.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

7 January 2021

Association of increased spontaneous mutation rates with high levels of transcription in yeast

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

7 January 2021

Expression of Bcl-2 protein is decreased in colorectal adenocarcinomas with microsatellite instability

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

7 January 2021

Allelic imbalance at chromosomal loci implicated in the pathogenesis of oral precancer, cumulative loss and its relationship with progression to cancer

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

7 January 2021

"Second hit" in sebaceous tumors from Muir-Torre patients with germline mutations in MSH2: allele loss is not the preferred mode of inactivation

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

7 January 2021

Widespread microsatellite instability in sebaceous tumours of patients with the Muir-Torre syndrome

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

7 January 2021

New mutation in the hMSH2 gene in a Spanish Muir-Torre syndrome

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

7 January 2021

An association between sebaceous carcinoma and microsatellite instability in immunosuppressed organ transplant recipients

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

7 January 2021

Analysis of microsatellite instability and loss of heterozygosity in keratoacanthoma

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

7 January 2021

Assessment of microsatellite instability and loss of heterozygosity in sporadic keratoacanthomas

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

7 January 2021

Hereditary non-polyposis colorectal cancer associated with disseminated superficial porokeratosis. Microsatellite instability in skin tumours

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

7 January 2021

A genetic model of melanoma tumorigenesis based on allelic losses

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

7 January 2021

Microsatellite instability in malignant melanoma

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

7 January 2021

Allelic imbalance in lichen sclerosus, hyperplasia, and intraepithelial neoplasia of the vulva

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

7 January 2021

Loss of heterozygosity in actinic keratosis, squamous cell carcinoma and sun-exposed normal-appearing skin in Japanese: difference between Japanese and Caucasians

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

7 January 2021

Genetic changes in sweat gland carcinomas

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0560.2002.290501.X

7 January 2021

10.1034/J.1600-0560.2002.290501.X

Identifiers

DOI

1 reference

4 August 2017

1 reference

PubMed ID

12100625