(Q57737936)

7

0 references

Alessandra Viel

object named as

Alessandra Viel

9

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Maurizio Genuardi

object named as

Maurizio Genuardi

8

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author name string

Chiara Pastrello

1

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Silvana Baglioni

2

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Maria Grazia Tibiletti

3

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Mara Fornasarig

5

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Alberto Morabito

European Journal of Human Genetics

6

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publication date

26 October 2005

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published in

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volume

14

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issue

1

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page(s)

63-68

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exact match

https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5201517

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cites work

Different molecular mechanisms underlie genomic deletions in the MLH1 Gene.

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Identification and characterization of genomic rearrangements of MSH2 and MLH1 in Lynch syndrome (HNPCC) by novel techniques

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Genomic deletions in MSH2 or MLH1 are a frequent cause of hereditary non-polyposis colorectal cancer: identification of novel and recurrent deletions by MLPA.

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Molecular analysis of hereditary nonpolyposis colorectal cancer in the United States: high mutation detection rate among clinically selected families and characterization of an American founder genomic deletion of the MSH2 gene

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Dosage analysis of cancer predisposition genes by multiplex ligation-dependent probe amplification

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Screening for genomic rearrangements of the MMR genes must be included in the routine diagnosis of HNPCC.

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Evaluation of tumor microsatellite instability using five quasimonomorphic mononucleotide repeats and pentaplex PCR.

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Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability

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Development of a fluorescent multiplex assay for detection of MSI-High tumors

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Quasimonomorphic mononucleotide repeats for high-level microsatellite instability analysis

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Testing tumors for microsatellite instability

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Mechanisms of inactivation of mismatch repair genes in human colorectal cancer cell lines: the predominant role of hMLH1.

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Germline, somatic and epigenetic events underlying mismatch repair deficiency in colorectal and HNPCC-related cancers.

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Tumor microsatellite-instability status as a predictor of benefit from fluorouracil-based adjuvant chemotherapy for colon cancer

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Hereditary nonpolyposis colorectal cancer and related conditions

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MSH2 genomic deletions are a frequent cause of HNPCC

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Mononucleotide repeats BAT-26 and BAT-25 accurately detect MSI-H tumors and predict tumor content: implications for population screening

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

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Tumor microsatellite instability and clinical outcome in young patients with colorectal cancer

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