Found: 19
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Aberrant succination of proteins in fumarate hydratase-deficient mice and HLRCC patients is a robust biomarker of mutation status.
- Published in:
- Journal of Pathology, 2011, v. 225, n. 1, p. 4, doi. 10.1002/path.2932
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- Publication type:
- Article
Assessment of Targeted and Non-Targeted Responses in Cells Deficient in <i>ATM</i> Function following Exposure to Low and High Dose X-Rays.
- Published in:
- PLoS ONE, 2014, v. 9, n. 3, p. 1, doi. 10.1371/journal.pone.0093211
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- Publication type:
- Article
Genome-wide allelotyping of 104 Finnish colorectal cancers reveals an excess of allelic imbalance in chromosome 20q in familial cases.
- Published in:
- Oncogene, 2003, v. 22, n. 14, p. 2206, doi. 10.1038/sj.onc.1206294
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- Article
Germline fumarate hydratase mutations in patients with ovarian mucinous cystadenoma.
- Published in:
- European Journal of Human Genetics, 2006, v. 14, n. 7, p. 880, doi. 10.1038/sj.ejhg.5201630
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- Publication type:
- Article
No germline FH mutations in familial breast cancer patients.
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- European Journal of Human Genetics, 2005, v. 13, n. 4, p. 506, doi. 10.1038/sj.ejhg.5201326
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- Publication type:
- Article
Multiple founder effects and geographical clustering of BRCA1 and BRCA2 families in Finland.
- Published in:
- European Journal of Human Genetics, 2000, v. 8, n. 10, p. 757, doi. 10.1038/sj.ejhg.5200529
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- Article
Increased HIF1α in SDH and FH deficient tumors does not cause microsatellite instability.
- Published in:
- International Journal of Cancer, 2007, v. 121, n. 6, p. 1386, doi. 10.1002/ijc.22819
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- Article
Analysis of fumarate hydratase mutations in a population-based series of early onset uterine leiomyosarcoma patients.
- Published in:
- International Journal of Cancer, 2006, v. 119, n. 2, p. 283, doi. 10.1002/ijc.21798
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- Publication type:
- Article
Little evidence for involvement of MLH3 in colorectal cancer predisposition.
- Published in:
- International Journal of Cancer, 2003, v. 106, n. 2, p. 292, doi. 10.1002/ijc.11218
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- Publication type:
- Article
Presence of Stromal Cells Enhances Epithelial-to-Mesenchymal Transition (EMT) Induction in Lung Bronchial Epithelium after Protracted Exposure to Oxidative Stress of Gamma Radiation.
- Published in:
- Oxidative Medicine & Cellular Longevity, 2019, p. 1, doi. 10.1155/2019/4120379
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- Publication type:
- Article
Analysis of a Finnish family confirms RHBDF2 mutations as the underlying factor in tylosis with esophageal cancer.
- Published in:
- Familial Cancer, 2012, v. 11, n. 3, p. 525, doi. 10.1007/s10689-012-9532-8
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- Article
No evidence for a genetic modifier for renal cell cancer risk in HLRCC syndrome.
- Published in:
- Familial Cancer, 2010, v. 9, n. 2, p. 245, doi. 10.1007/s10689-009-9312-2
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- Publication type:
- Article
Array comparative genomic hybridization identifies a distinct DNA copy number profile in renal cell cancer associated with hereditary leiomyomatosis and renal cell cancer.
- Published in:
- Genes, Chromosomes & Cancer, 2009, v. 48, n. 7, p. 544, doi. 10.1002/gcc.20663
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- Publication type:
- Article
Analysis of 11q21-24 loss of heterozygosity candidate target genes in breast cancer: Indications of TSLC1 promoter hypermethylation.
- Published in:
- Genes, Chromosomes & Cancer, 2002, v. 34, n. 4, p. 384, doi. 10.1002/gcc.10079
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- Publication type:
- Article
Loss of heterozygosity at 11q23.1 and survival in breast cancer: Results of a large European study.
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- Genes, Chromosomes & Cancer, 1999, v. 25, n. 3, p. 212, doi. 10.1002/(SICI)1098-2264(199907)25:3<212::AID-GCC3>3.0.CO;2-G
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- Article
Analysis of KLHDC8B in familial nodular lymphocyte predominant Hodgkin lymphoma.
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- British Journal of Haematology, 2011, v. 154, n. 3, p. 413, doi. 10.1111/j.1365-2141.2010.08528.x
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- Article
Mutations in the human LKB1/STK11 gene.
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- 2005
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- Publication type:
- Other
DNA methylation patterns in hereditaryhuman cancers mimic sporadic tumorigenesis.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 26, p. 3001, doi. 10.1093/hmg/10.26.3001
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- Publication type:
- Article
The FH mutation database: an online database of fumarate hydratase mutations involved in the MCUL (HLRCC) tumor syndrome and congenital fumarase deficiency.
- Published in:
- BMC Medical Genetics, 2008, v. 9, p. 1, doi. 10.1186/1471-2350-9-20
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- Publication type:
- Article