Found: 28
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Gene-environment interaction in hereditary nonpolyposis colorectal cancer with implications for diagnosis and genetic testing.
- Published in:
- International Journal of Cancer, 1999, v. 82, n. 4, p. 516, doi. 10.1002/(SICI)1097-0215(19990812)82:4<516::AID-IJC8>3.0.CO;2-U
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- Article
Germline variants in POLE are associated with early onset mismatch repair deficient colorectal cancer.
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- European Journal of Human Genetics, 2015, v. 23, n. 8, p. 1080, doi. 10.1038/ejhg.2014.242
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- Article
Genetic variant in the telomerase gene modifies cancer risk in Lynch syndrome.
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- European Journal of Human Genetics, 2013, v. 21, n. 5, p. 511, doi. 10.1038/ejhg.2012.204
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- Article
Suspected HNPCC and Amsterdam criteria II: evaluation of mutation detection rate, an international collaborative study.
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- International Journal of Colorectal Disease, 2002, v. 17, n. 2, p. 109, doi. 10.1007/s003840100348
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- Article
A review of the genetic background and tumour profiling in familial colorectal cancer.
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- Mutagenesis, 2012, v. 27, n. 2, p. 239, doi. 10.1093/mutage/ger071
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- Article
8q23.3 and 11q23.1 as modifying loci influencing the risk for CRC in Lynch syndrome.
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- European Journal of Human Genetics, 2012, v. 20, n. 5, p. 487, doi. 10.1038/ejhg.2011.232
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- Article
Long-term follow-up of recipients of allogeneic bone marrow grafts reveals no progressive telomere shortening and provides no evidence for haematopoietic stem cell exhaustion.
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- British Journal of Haematology, 2002, v. 116, n. 2, p. 491, doi. 10.1046/j.1365-2141.2002.03283.x
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- Article
SNP association study in PMS2-associated Lynch syndrome.
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- Familial Cancer, 2018, v. 17, n. 4, p. 507, doi. 10.1007/s10689-017-0061-3
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- Article
Excluding Lynch syndrome in a female patient with metachronous DNA mismatch repair deficient colon- and ovarian cancer.
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- Familial Cancer, 2018, v. 17, n. 3, p. 415, doi. 10.1007/s10689-017-0055-1
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- Article
Exome Sequencing of Germline DNA from Non-BRCA1/2 Familial Breast Cancer Cases Selected on the Basis of aCGH Tumor Profiling.
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- PLoS ONE, 2013, v. 8, n. 1, p. 1, doi. 10.1371/journal.pone.0055734
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- Article
A genetic variant in telomerase reverse transcriptase (TERT) modifies cancer risk in Lynch syndrome patients harbouring pathogenic MSH2 variants.
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- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-90501-2
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- Article
A procedure for the detection of linkage with high density SNP arrays in a large pedigree with colorectal cancer.
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- BMC Cancer, 2007, v. 7, p. 6, doi. 10.1186/1471-2407-7-6
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- Article
Quantification of sequence exchange events between PMS2 and PMS2CL provides a basis for improved mutation scanning of lynch syndrome patients.
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- Human Mutation, 2010, v. 31, n. 5, p. 578, doi. 10.1002/humu.21229
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- Article
A cell-free assay for the functional analysis of variants of the mismatch repair protein MLH1.
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- Human Mutation, 2010, v. 31, n. 3, p. 247, doi. 10.1002/humu.21180
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- Article
Intronic variants in BRCA1 and BRCA2 that affect RNA splicing can be reliably selected by splice-site prediction programs.
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- Human Mutation, 2009, v. 30, n. 1, p. 107, doi. 10.1002/humu.20811
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- Article
Adenosine Deaminase Complexing Protein in Transformed Cells and Colon Cancer.
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- Annals of the New York Academy of Sciences, 1985, v. 451, n. 1, p. 324, doi. 10.1111/j.1749-6632.1985.tb27129.x
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- Article
Insertion of an SVA element, a nonautonomous retrotransposon, in PMS2 intron 7 as a novel cause of lynch syndrome.
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- Human Mutation, 2012, v. 33, n. 7, p. 1051, doi. 10.1002/humu.22092
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- Publication type:
- Article
Macrophages inhibit human osteosarcoma cell growth after activation with the bacterial cell wall derivative liposomal muramyl tripeptide in combination with interferon-γ.
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- Journal of Experimental & Clinical Cancer Research (17569966), 2014, v. 33, n. 1, p. 1, doi. 10.1186/1756-9966-33-27
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- Article
Splicing analysis for exonic and intronic mismatch repair gene variants associated with Lynch syndrome confirms high concordance between minigene assays and patient RNA analyses.
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- Molecular Genetics & Genomic Medicine, 2015, v. 3, n. 4, p. 327, doi. 10.1002/mgg3.145
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- Article
Reply to Win and Jenkins.
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- International Journal of Cancer, 2013, v. 133, n. 7, p. 1764, doi. 10.1002/ijc.28178
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- Article
Combined analysis of three lynch syndrome cohorts confirms the modifying effects of 8q23.3 and 11q23.1 in MLH1 mutation carriers.
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- International Journal of Cancer, 2013, v. 132, n. 7, p. 1556, doi. 10.1002/ijc.27843
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- Article
The risk of extra-colonic, extra-endometrial cancer in the Lynch syndrome.
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- International Journal of Cancer, 2008, v. 123, n. 2, p. 444, doi. 10.1002/ijc.23508
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- Article
The importance of a large sample cohort for studies on modifier genes influencing disease severity in FAP patients.
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- Hereditary Cancer in Clinical Practice, 2013, v. 11, n. 1, p. 1, doi. 10.1186/1897-4287-11-20
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- Article
Whole Gene Capture Analysis of 15 CRC Susceptibility Genes in Suspected Lynch Syndrome Patients.
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- PLoS ONE, 2016, v. 11, n. 6, p. 1, doi. 10.1371/journal.pone.0157381
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- Article
Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia.
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- 2018
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- Publication type:
- journal article
Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia.
- Published in:
- British Journal of Cancer, 2017, v. 117, n. 8, p. 1215, doi. 10.1038/bjc.2017.240
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- Article
Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia.
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- British Journal of Cancer, 2017, v. 117, n. 6, p. 876, doi. 10.1038/bjc.2017.240
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- Article
Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia.
- Published in:
- 2017
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- Publication type:
- journal article