Found: 19
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Novel strategy for optimal sequential application of clinical criteria, immunohistochemistry and microsatellite analysis in the diagnosis of hereditary nonpolyposis colorectal cancer.
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- International Journal of Cancer, 2006, v. 118, n. 1, p. 115, doi. 10.1002/ijc.21313
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- Article
Involvement of hMSH6 in the development of hereditary and sporadic colorectal cancer revealed by immunostaining is based on germline mutations, but rarely on somatic inactivation.
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- International Journal of Cancer, 2002, v. 97, n. 5, p. 643, doi. 10.1002/ijc.10097
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Sequence analysis of the mismatch repair gene hMSH6 in the germline of patients with familial and sporadic colorectal cancer.
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- International Journal of Cancer, 2000, v. 85, n. 5, p. 606, doi. 10.1002/(SICI)1097-0215(20000301)85:5<606::AID-IJC2>3.0.CO;2-B
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Identification of microsatellite instability and mismatch repair gene mutations in breast cancer cell lines.
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- Genes, Chromosomes & Cancer, 2003, v. 37, n. 1, p. 29, doi. 10.1002/gcc.10196
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Aberrant protein expression and frequent allelic loss of MSH3 in colorectal cancer with low-level microsatellite instability.
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- International Journal of Colorectal Disease, 2012, v. 27, n. 7, p. 911, doi. 10.1007/s00384-011-1408-0
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- Article
TCF-3, 4 protein expression correlates with β-catenin expression in MSS and MSI-H colorectal cancer from HNPCC patients but not in sporadic colorectal cancers.
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- International Journal of Colorectal Disease, 2010, v. 25, n. 8, p. 931, doi. 10.1007/s00384-010-0959-9
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- Article
N-Acetyltransferase (NAT) 2 acetylator status and age of tumour onset in patients with sporadic and familial, microsatellite stable (MSS) colorectal cancer.
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- International Journal of Colorectal Disease, 2007, v. 22, n. 2, p. 137, doi. 10.1007/s00384-006-0171-0
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Combined molecular and clinical approach for decision making for surgery in HNPCC patients: a report on three cases in two families.
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- International Journal of Colorectal Disease, 2001, v. 16, n. 6, p. 402, doi. 10.1007/s003840100349
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- Article
Clinical consequences of molecular diagnosis in families with mismatch repair gene germline mutations.
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- International Journal of Colorectal Disease, 2000, v. 15, n. 5/6, p. 255, doi. 10.1007/s003840000261
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Compound heterozygosity for two MSH6 mutations in a patient with early onset of HNPCC-associated cancers, but without hematological malignancy and brain tumor.
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- European Journal of Human Genetics, 2006, v. 14, n. 5, p. 561, doi. 10.1038/sj.ejhg.5201568
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- Article
Molecular Mechanisms Associated with Chromosomal and Microsatellite Instability in Sporadic Glioblastoma multiforme.
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- Oncology, 2004, v. 66, n. 5, p. 395, doi. 10.1159/000079488
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Microsatellite instability and loss of heterozygosity in squamous cell carcinoma of the head and neck.
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- Head & Neck, 2008, v. 30, n. 8, p. 1105, doi. 10.1002/hed.20857
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- Article
Ten novel MSH2 and MLH1 germline mutations in families with HNPCC.
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- Human Mutation, 2004, v. 24, n. 4, p. 351, doi. 10.1002/humu.9278
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Eight novel MSH6 germline mutations in patients with familial and nonfamilial colorectal cancer selected by loss of protein expression in tumor tissue (Communicated by Daniel Schorderet) Online Citation: Human Mutation, Mutation in Brief #688 (2004) Online http://www3.interscience.wiley.com/homepages/38515/pdf/mutation/688.pdf)
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- Human Mutation, 2004, v. 23, n. 3, p. 285
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- Article
Identification of six novel MSH2 and MLH1 germline mutations in HNPCC (Communicated by Mark H. Paalman) Online Citation: Human Mutation, Mutation in Brief #592 (2002) Online http://www.interscience.wiley.com/humanmutation/pdf/mutation/592.pdf).
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- Human Mutation, 2003, v. 21, n. 4, p. 445, doi. 10.1002/humu.9121
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- Article
Identification of six novel MSH2 and MLH1 germline mutations in HNPCCCommunicated by Mark H. PaalmanOnline Citation: Human Mutation, Mutation in Brief #592 (2002) Onlinehttp://www.interscience.wiley.com/humanmutation/pdf/mutation/592.pdf.
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- Human Mutation, 2003, v. 21, n. 4, p. 445, doi. 10.1002/humu.9121
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- Article
Seven novel MLH1 and MSH2 germline mutations in hereditary nonpolyposis colorectal cancer.
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- Human Mutation, 2002, v. 19, n. 1, p. 82, doi. 10.1002/humu.9004
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- Article
Quantitative Differences between Aberrant Transcripts Which Occur as Common Isoforms and due to Mutation-based Exon Skipping of the Mismatch Repair Gene hMLH1.
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- Clinical Chemistry & Laboratory Medicine, 1999, v. 37, n. 9, p. 883
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A microsatellite map of wheat.
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- Genetics, 1998, v. 149, n. 4, p. 2007, doi. 10.1093/genetics/149.4.2007
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- Article