Found: 97
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Comprehensive genetic analysis of seven large families with mismatch repair proficient colorectal cancer.
- Published in:
- Genes, Chromosomes & Cancer, 2010, v. 49, n. 6, p. 539, doi. 10.1002/gcc.20763
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- Publication type:
- Article
Genome-wide linkage scan in Dutch hereditary non-BRCA1/2 breast cancer families identifies 9q21-22 as a putative breast cancer susceptibility locus.
- Published in:
- Genes, Chromosomes & Cancer, 2008, v. 47, n. 11, p. 947, doi. 10.1002/gcc.20597
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- Publication type:
- Article
A targeted mouse Brca1 mutation removing the last BRCT repeat results in apoptosis and embryonic lethality at the headfold stage.
- Published in:
- Oncogene, 2001, v. 20, n. 20, p. 2544, doi. 10.1038/sj.onc.1204363
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- Publication type:
- Article
Absence of evidence for a familial breast cancer susceptibility gene at chromosome 8p12-p22.
- Published in:
- Oncogene, 2000, v. 19, n. 36, p. 4170, doi. 10.1038/sj.onc.1203735
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- Publication type:
- 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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- Publication type:
- Article
Searching for susceptibility alleles: Emphasis on bilateral breast cancer.
- Published in:
- International Journal of Cancer, 2007, v. 121, n. 4, p. 921, doi. 10.1002/ijc.22785
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- Publication type:
- Article
NBS1 657del5 mutation may contribute only to a limited fraction of breast cancer cases in Russia.
- Published in:
- International Journal of Cancer, 2005, v. 114, n. 4, p. 585, doi. 10.1002/ijc.20765
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- Publication type:
- Article
Mutant BRCA1 alleles transmission: Different approaches and different biases.
- Published in:
- International Journal of Cancer, 2005, v. 113, n. 1, p. 166, doi. 10.1002/ijc.20541
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- Publication type:
- Article
Association between BRCA1 and BRCA2 mutations and cancer phenotype in Spanish breast/ovarian cancer families: Implications for genetic testing.
- Published in:
- International Journal of Cancer, 2002, v. 97, n. 4, p. 466, doi. 10.1002/ijc.1627
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- Publication type:
- Article
Prevalence of founder BRCA1 and BRCA2 mutations among breast and ovarian cancer patients in hungary.
- Published in:
- International Journal of Cancer, 2000, v. 86, n. 5, p. 737, doi. 10.1002/(SICI)1097-0215(20000601)86:5<737::AID-IJC21>3.0.CO;2-1
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- Publication type:
- Article
BRCA1-related breast cancer in Austrian breast and ovarian cancer families: Specific BRCA1 mutations and pathological characteristics.
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- International Journal of Cancer, 1998, v. 77, n. 3, p. 354, doi. 10.1002/(SICI)1097-0215(19980729)77:3<354::AID-IJC8>3.0.CO;2-N
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- Publication type:
- Article
RNF12 is regulated by AKT phosphorylation and promotes TGF-β driven breast cancer metastasis.
- Published in:
- Cell Death & Disease, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41419-021-04493-y
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- Publication type:
- Article
Similar gene expression profiles of sporadic, PGL2-, and SDHD-linked paragangliomas suggest a common pathway to tumorigenesis.
- Published in:
- BMC Medical Genomics, 2009, v. 2, p. 1, doi. 10.1186/1755-8794-2-25
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- Publication type:
- Article
Multi-gene panel testing and association analysis in Cypriot breast cancer cases and controls.
- Published in:
- Frontiers in Genetics, 2023, p. 1, doi. 10.3389/fgene.2023.1248492
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- Publication type:
- Article
A new conditional Apc-mutant mouse model for colorectal cancer.
- Published in:
- Carcinogenesis, 2010, v. 31, n. 5, p. 946, doi. 10.1093/carcin/bgq046
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- Publication type:
- Article
5-Aminosalicylic acid inhibits colitis-associated but not sporadic colorectal neoplasia in a novel conditional Apc mouse model.
- Published in:
- Carcinogenesis, 2009, v. 30, n. 7, p. 1217, doi. 10.1093/carcin/bgp113
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- Publication type:
- Article
Nuclear receptor NR4A1 promotes breast cancer invasion and metastasis by activating TGF-β signalling.
- Published in:
- Nature Communications, 2014, v. 5, n. 3, p. 3388, doi. 10.1038/ncomms4388
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- Publication type:
- Article
CHEK2*1100delC homozygosity in the Netherlands-prevalence and risk of breast and lung cancer.
- Published in:
- European Journal of Human Genetics, 2014, v. 22, n. 1, p. 46, doi. 10.1038/ejhg.2013.85
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- Publication type:
- Article
Serrated adenomas and mixed polyposis caused by a splice acceptor deletion in the mouse Smad4 gene.
- Published in:
- Genes, Chromosomes & Cancer, 2003, v. 36, n. 3, p. 273, doi. 10.1002/gcc.10169
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- Publication type:
- Article
Nearly all hereditary paragangliomas in The Netherlands are caused by two founder mutations in the SDHD gene.
- Published in:
- Genes, Chromosomes & Cancer, 2001, v. 31, n. 3, p. 274, doi. 10.1002/gcc.1144
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- Publication type:
- Article
Allelotype analysis of flow-sorted breast cancer cells demonstrates genetically related diploid and aneuploid subpopulations in primary tumors and lymph node metastases.
- Published in:
- Genes, Chromosomes & Cancer, 2000, v. 28, n. 2, p. 173, doi. 10.1002/(SICI)1098-2264(200006)28:2<173::AID-GCC6>3.0.CO;2-1
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- Publication type:
- Article
A sporadic breast tumor with a somatically acquired complex genomic rearrangement in BRCA1.
- Published in:
- Genes, Chromosomes & Cancer, 2000, v. 27, n. 3, p. 295, doi. 10.1002/(SICI)1098-2264(200003)27:3<295::AID-GCC10>3.0.CO;2-F
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- Publication type:
- Article
TP53 mutations and breast cancer prognosis: Particularly poor survival rates for cases with mutations in the zinc-binding domains.
- Published in:
- Genes, Chromosomes & Cancer, 1995, v. 14, n. 1, p. 71, doi. 10.1002/gcc.2870140113
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- Publication type:
- Article
Allelotype of head and neck paragangliomas: Allelic imbalance is confined to the long arm of chromosome 11, the site of the predisposing locus PGL.
- Published in:
- Genes, Chromosomes & Cancer, 1994, v. 11, n. 2, p. 71, doi. 10.1002/gcc.2870110202
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- Publication type:
- Article
At least two different regions are involved in allelic imbalance on chromosome arm 16q in breast cancer.
- Published in:
- Genes, Chromosomes & Cancer, 1994, v. 9, n. 2, p. 101, doi. 10.1002/gcc.2870090205
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- Publication type:
- Article
Re: Oral contraceptives and the risk of breast cancer in BRCA1 and BRCA2 mutation carriers.
- Published in:
- 2003
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- Publication type:
- commentary
Somatic loss of maternal chromosome 11 causes parent-of-origin-dependent inheritance in SDHD-linked paraganglioma and phaeochromocytoma families.
- Published in:
- Oncogene, 2004, v. 23, n. 23, p. 4076, doi. 10.1038/sj.onc.1207591
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- Publication type:
- Article
Fractional allelic imbalance in human breast cancer increases with tetraploidization and chromosome loss.
- Published in:
- International Journal of Cancer, 1992, v. 50, n. 4, p. 544, doi. 10.1002/ijc.2910500408
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- Publication type:
- Article
Hypothesis: Why Different Types of SDH Gene Variants Cause Divergent Tumor Phenotypes.
- Published in:
- Genes, 2022, v. 13, n. 6, p. 1025, doi. 10.3390/genes13061025
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- Publication type:
- Article
MYLK and PTGS1 Genetic Variations Associated with Osteoporosis and Benign Breast Tumors in Korean Women.
- Published in:
- Genes, 2021, v. 12, n. 3, p. 378, doi. 10.3390/genes12030378
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- Publication type:
- Article
The Dutch founder mutation SDHD.D92Y shows a reduced penetrance for the development of paragangliomas in a large multigenerational family.
- Published in:
- European Journal of Human Genetics, 2010, v. 18, n. 1, p. 62, doi. 10.1038/ejhg.2009.112
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- Publication type:
- Article
Unclassified variants in disease-causing genes: nonuniformity of genetic testing and counselling, a proposal for guidelines.
- Published in:
- 2005
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- Publication type:
- Letter
Men at risk of being a mutation carrier for hereditary breast/ovarian cancer: an exploration of attitudes and psychological functioning during genetic testing.
- Published in:
- European Journal of Human Genetics, 2001, v. 9, n. 7, p. 492, doi. 10.1038/sj.ejhg.5200668
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- Publication type:
- Article
A high-resolution integrated map spanning the SDHD gene at 11q23: a 1.1-Mb BAC contig, a partial transcript map and 15 new repeat polymorphisms in a tumour-suppressor region.
- Published in:
- European Journal of Human Genetics, 2001, v. 9, n. 2, p. 121, doi. 10.1038/sj.ejhg.5200585
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- Publication type:
- Article
The "Psychosocial Aspects in Hereditary Cancer" questionnaire in women attending breast cancer genetic clinics: Psychometric validation across French‐, German‐ and Spanish‐language versions.
- Published in:
- European Journal of Cancer Care, 2020, v. 29, n. 1, p. N.PAG, doi. 10.1111/ecc.13173
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- Publication type:
- Article
Mutations in SLC29A3, Encoding an Equilibrative Nucleoside Transporter ENT3, Cause a Familial Histiocytosis Syndrome (Faisalabad Histiocytosis) and Familial Rosai-Dorfman Disease.
- Published in:
- PLoS Genetics, 2010, v. 6, n. 2, p. 1, doi. 10.1371/journal.pgen.1000833
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- Publication type:
- Article
Prediction of contralateral breast cancer: external validation of risk calculators in 20 international cohorts.
- Published in:
- Breast Cancer Research & Treatment, 2020, v. 181, n. 2, p. 423, doi. 10.1007/s10549-020-05611-8
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- Publication type:
- Article
Survival after bilateral risk-reducing mastectomy in healthy BRCA1 and BRCA2 mutation carriers.
- Published in:
- Breast Cancer Research & Treatment, 2019, v. 177, n. 3, p. 723, doi. 10.1007/s10549-019-05345-2
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- Publication type:
- Article
Response.
- Published in:
- 2016
- By:
- Publication type:
- letter
Prediction and clinical utility of a contralateral breast cancer risk model.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Genetic clinicians' confidence in BOADICEA comprehensive breast cancer risk estimates and counselees' psychosocial outcomes: A prospective study.
- Published in:
- Clinical Genetics, 2022, v. 102, n. 1, p. 30, doi. 10.1111/cge.14147
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- Publication type:
- Article
Long-term in vitro 2D-culture of SDHB and SDHD-related human paragangliomas and pheochromocytomas.
- Published in:
- PLoS ONE, 2022, v. 17, n. 9, p. 1, doi. 10.1371/journal.pone.0274478
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- Publication type:
- Article
Germline DLST Variants Promote Epigenetic Modifications in Pheochromocytoma-Paraganglioma.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2021, v. 106, n. 2, p. 459, doi. 10.1210/clinem/dgaa819
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- Publication type:
- Article
Corrections to: Use of the BOADICEA Web Application in clinical practice: appraisals by clinicians from various countries.
- Published in:
- Familial Cancer, 2018, v. 17, n. 3, p. 469, doi. 10.1007/s10689-017-0051-5
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- Publication type:
- Article
Use of the BOADICEA Web Application in clinical practice: appraisals by clinicians from various countries.
- Published in:
- Familial Cancer, 2018, v. 17, n. 1, p. 31, doi. 10.1007/s10689-017-0014-x
- By:
- Publication type:
- Article
High-resolution melting (HRM) re-analysis of a polyposis patients cohort reveals previously undetected heterozygous and mosaic APC gene mutations.
- Published in:
- Familial Cancer, 2015, v. 14, n. 2, p. 247, doi. 10.1007/s10689-015-9780-5
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- Publication type:
- Article
Founder mutations in early-onset, familial and bilateral breast cancer patients from Russia.
- Published in:
- Familial Cancer, 2007, v. 6, n. 3, p. 281, doi. 10.1007/s10689-007-9120-5
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- Publication type:
- Article
High-throughput automated scoring of Ki67 in breast cancer tissue microarrays from the Breast Cancer Association Consortium.
- Published in:
- Journal of Pathology: Clinical Research, 2016, v. 2, n. 3, p. 138, doi. 10.1002/cjp2.42
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- Publication type:
- Article
Correction: PredictCBC-2.0: a contralateral breast cancer risk prediction model developed and validated in ~ 200,000 patients.
- Published in:
- 2022
- By:
- Publication type:
- corrected article
PredictCBC-2.0: a contralateral breast cancer risk prediction model developed and validated in ~ 200,000 patients.
- Published in:
- 2022
- By:
- Publication type:
- journal article