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Lifestyle Characteristics in Women Carriers of BRCA Mutations: Results From an Italian Trial Cohort.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Gene linkage analysis and DNA based detection of autosomal dominant polycystic kidney disease (ADPKD) in a newborn infant. Case report.
- Published in:
- Journal of Perinatal Medicine, 1995, v. 23, n. 3, p. 205
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- Publication type:
- Article
Prevalence of BRCA homopolymeric indels in an ION Torrent-based tumour-to-germline testing workflow in high-grade ovarian carcinoma.
- Published in:
- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-33857-x
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- Publication type:
- Article
Mutational screening of the RB1 gene in Italian patients with retinoblastoma reveals 11 novel mutations.
- Published in:
- Journal of Human Genetics, 2006, v. 51, n. 3, p. 209, doi. 10.1007/s10038-005-0348-3
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- Publication type:
- Article
Prenatal diagnosis of autosomal dominant polycystic kidney disease using flanking DNA markers and the polymerase chain reaction.
- Published in:
- Prenatal Diagnosis, 1992, v. 12, n. 6, p. 513, doi. 10.1002/pd.1970120606
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- Publication type:
- Article
Characterization of an Italian Founder Mutation in the RING-Finger Domain of <i>BRCA1</i>.
- Published in:
- PLoS ONE, 2014, v. 9, n. 2, p. 1, doi. 10.1371/journal.pone.0086924
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- Publication type:
- Article
miR-342 Regulates BRCA1 Expression through Modulation of ID4 in Breast Cancer.
- Published in:
- PLoS ONE, 2014, v. 9, n. 1, p. 1, doi. 10.1371/journal.pone.0087039
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- Publication type:
- Article
Comparative <i>In Vitro</i> and <i>In Silico</i> Analyses of Variants in Splicing Regions of <i>BRCA1</i> and <i>BRCA2</i> Genes and Characterization of Novel Pathogenic Mutations.
- Published in:
- PLoS ONE, 2013, v. 8, n. 2, p. 1, doi. 10.1371/journal.pone.0057173
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- Publication type:
- Article
Sequencing Analysis of SLX4/FANCP Gene in Italian Familial Breast Cancer Cases.
- Published in:
- PLoS ONE, 2012, v. 7, n. 2, p. 1, doi. 10.1371/journal.pone.0031038
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- Publication type:
- Article
Risk‐reducing surgery in BRCA1/BRCA2 mutation carriers: Are there factors associated with the choice?
- Published in:
- Psycho-Oncology, 2019, v. 28, n. 9, p. 1871, doi. 10.1002/pon.5166
- By:
- Publication type:
- Article
Risk-reducing surgery in BRCA1/BRCA2 mutation carriers: Are there factors associated with the choice?
- Published in:
- 2019
- By:
- Publication type:
- journal article
Re: Molecular Basis for Estrogen Receptor a Deficiency in BRCA1 -Linked Breast Cancer.
- Published in:
- 2008
- By:
- Publication type:
- Letter
Loss of tyrosinase activity confers increased skin tumor susceptibility in mice.
- Published in:
- Oncogene, 2004, v. 23, n. 23, p. 4130, doi. 10.1038/sj.onc.1207565
- By:
- Publication type:
- Article
Allele-specific patterns of the mouse parathyroid hormone-related protein: influences on cell adhesion and migration.
- Published in:
- Oncogene, 2003, v. 22, n. 49, p. 7711, doi. 10.1038/sj.onc.1207088
- By:
- Publication type:
- Article
Analysis of Italian BRCA1/2 Pathogenic Variants Identifies a Private Spectrum in the Population from the Bergamo Province in Northern Italy.
- Published in:
- Cancers, 2021, v. 13, n. 3, p. 532, doi. 10.3390/cancers13030532
- By:
- Publication type:
- Article
BRCA1/2 Variants and Metabolic Factors: Results From a Cohort of Italian Female Carriers.
- Published in:
- Cancers, 2020, v. 12, n. 12, p. 3584, doi. 10.3390/cancers12123584
- By:
- Publication type:
- Article
Analysis of BRCA1 and RAD51C Promoter Methylation in Italian Families at High-Risk of Breast and Ovarian Cancer.
- Published in:
- Cancers, 2020, v. 12, n. 4, p. 910, doi. 10.3390/cancers12040910
- By:
- Publication type:
- Article
Constitutive BRCA1 Promoter Hypermethylation Can Be a Predisposing Event in Isolated Early-Onset Breast Cancer.
- Published in:
- Cancers, 2019, v. 11, n. 1, p. 58, doi. 10.3390/cancers11010058
- By:
- Publication type:
- Article
A Dietary Intervention to Lower Serum Levels of IGF-I in BRCA Mutation Carriers.
- Published in:
- Cancers, 2018, v. 10, n. 9, p. 309, doi. 10.3390/cancers10090309
- By:
- Publication type:
- Article
Adherence to Mediterranean Diet and Metabolic Syndrome in BRCA Mutation Carriers.
- Published in:
- Integrative Cancer Therapies, 2018, v. 17, n. 1, p. 153, doi. 10.1177/1534735417721015
- By:
- Publication type:
- Article
The SNP rs895819 in miR-27a is not associated with familial breast cancer risk in Italians.
- Published in:
- 2012
- By:
- Publication type:
- Letter
Two new CHEK2 germ-line variants detected in breast cancer/sarcoma families negative for BRCA1, BRCA2, and TP53 gene mutations.
- Published in:
- Breast Cancer Research & Treatment, 2011, v. 130, n. 1, p. 207, doi. 10.1007/s10549-011-1548-5
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- Publication type:
- Article
Evidence for a link between TNFRSF11A and risk of breast cancer.
- Published in:
- Breast Cancer Research & Treatment, 2011, v. 129, n. 3, p. 947, doi. 10.1007/s10549-011-1546-7
- By:
- Publication type:
- Article
PALB2 germline mutations in familial breast cancer cases with personal and family history of pancreatic cancer.
- Published in:
- 2011
- By:
- Publication type:
- Letter
The CASP8 rs3834129 polymorphism and breast cancer risk in BRCA1 mutation carriers.
- Published in:
- Breast Cancer Research & Treatment, 2011, v. 125, n. 3, p. 855, doi. 10.1007/s10549-010-1068-8
- By:
- Publication type:
- Article
Four new cases of double heterozygosity for BRCA1 and BRCA2 gene mutations: clinical, pathological, and family characteristics.
- Published in:
- 2011
- By:
- Publication type:
- Report
A cancer modifier role for parathyroid hormone-related protein.
- Published in:
- Oncogene, 2000, v. 19, n. 47, p. 5324, doi. 10.1038/sj.onc.1203916
- By:
- Publication type:
- Article
Mapping of Melanoma Modifier Loci in RET Transgenic Mice.
- Published in:
- Cancer Science, 2000, v. 91, n. 11, p. 1142, doi. 10.1111/j.1349-7006.2000.tb00897.x
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- Publication type:
- Article
SNPs in ultraconserved elements and familial breast cancer risk.
- Published in:
- Carcinogenesis, 2009, v. 30, n. 3, p. 544, doi. 10.1093/carcin/bgn289
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- Publication type:
- Article
Inhibition of both skin and lung tumorigenesis by Car-R mouse-derived cancer modifier loci.
- Published in:
- International Journal of Cancer, 2002, v. 97, n. 5, p. 580, doi. 10.1002/ijc.10104
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- Publication type:
- Article
Cutaneous Melanoma in Childhood and Adolescence Shows Frequent Loss of INK4A and Gain of KIT.
- Published in:
- Journal of Investigative Dermatology, 2009, v. 129, n. 7, p. 1759, doi. 10.1038/jid.2008.422
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- Publication type:
- Article
Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 16, p. 3304
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- Publication type:
- Article
Revertant mosaicism for family mutations is not observed in BRCA1/2 phenocopies.
- Published in:
- PLoS ONE, 2017, v. 12, n. 2, p. 1, doi. 10.1371/journal.pone.0171663
- By:
- Publication type:
- Article
Thyroid findings in pediatric and adult patients with PTEN hamartoma tumor syndrome: A retrospective analysis, and literature review.
- Published in:
- Endocrine (1355008X), 2023, v. 81, n. 1, p. 98, doi. 10.1007/s12020-023-03313-x
- By:
- Publication type:
- Article
Increased access to TP53 analysis through breast cancer multi-gene panels: clinical considerations.
- Published in:
- Familial Cancer, 2018, v. 17, n. 3, p. 317, doi. 10.1007/s10689-017-0020-z
- By:
- Publication type:
- Article
Estimate of the penetrance of BRCA mutation and the COS software for the assessment of BRCA mutation probability.
- Published in:
- Familial Cancer, 2015, v. 14, n. 1, p. 117, doi. 10.1007/s10689-014-9766-8
- By:
- Publication type:
- Article
Serum levels of IGF-I and BRCA penetrance: a case control study in breast cancer families.
- Published in:
- Familial Cancer, 2011, v. 10, n. 3, p. 521, doi. 10.1007/s10689-011-9437-y
- By:
- Publication type:
- Article
Use of intercross outbred mice and single nucleotide polymorphisms to map skin cancer modifier loci.
- Published in:
- Mammalian Genome, 2001, v. 12, n. 4, p. 291, doi. 10.1007/s003350010274
- By:
- Publication type:
- Article
Linkage disequilibrium and haplotype mapping of a skin cancer susceptibility locus in outbred mice.
- Published in:
- Mammalian Genome, 2000, v. 11, n. 11, p. 979, doi. 10.1007/s003350010184
- By:
- Publication type:
- Article
The Impact of Mediterranean Dietary Intervention on Metabolic and Hormonal Parameters According to BRCA1/2 Variant Type.
- Published in:
- Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.820878
- By:
- Publication type:
- Article
Whole-exome sequencing and targeted gene sequencing provide insights into the role of PALB2 as a male breast cancer susceptibility gene.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Identification of fifteen novel germline variants in the BRCA1 3′UTR reveals a variant in a breast cancer case that introduces a functional miR-103 target site.
- Published in:
- Human Mutation, 2012, v. 33, n. 12, p. 1665, doi. 10.1002/humu.22159
- By:
- Publication type:
- Article
The CHEK2 c.1100delC mutation plays an irrelevant role in breast cancer predisposition in Italy.
- Published in:
- Human Mutation, 2004, v. 24, n. 1, p. 100, doi. 10.1002/humu.20051
- By:
- Publication type:
- Article
Management of BRCA Tumour Testing in an Integrated Molecular Tumour Board Multidisciplinary Model.
- Published in:
- Frontiers in Oncology, 2022, v. 12, p. 1, doi. 10.3389/fonc.2022.857515
- By:
- Publication type:
- Article
Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 22, p. 4442, doi. 10.1093/hmg/ddp372
- By:
- Publication type:
- Article
Genetic Variants and Somatic Alterations Associated with MITF-E318K Germline Mutation in Melanoma Patients.
- Published in:
- Genes, 2021, v. 12, n. 9, p. 1440, doi. 10.3390/genes12091440
- By:
- Publication type:
- Article
A novel frameshift deletion in type IV collagen α5 gene in a juvenile-type Alport syndrome patient: An adenine deletion (2940/2943 del A) in exon 34 of COL4A5.
- Published in:
- Human Mutation, 1994, v. 3, n. 4, p. 386, doi. 10.1002/humu.1380030410
- By:
- Publication type:
- Article
Genetic Variation at 9p22.2 and Ovarian Cancer Risk for BRCA1 and BRCA2 Mutation Carriers.
- Published in:
- JNCI: Journal of the National Cancer Institute, 2011, v. 103, n. 2, p. 105, doi. 10.1093/jnci/djq494
- By:
- Publication type:
- Article
Single base pair deletions in exons 39 and 42 of the COL4A5 gene in Alport syndrome.
- Published in:
- Human Molecular Genetics, 1994, v. 3, n. 1, p. 201
- By:
- Publication type:
- Article
Linkage analysis for the diagnosis of autosomal dominant polycystic kidney disease, and for the determination of genetic heterogeneity in Italian families.
- Published in:
- Clinical Genetics, 1991, v. 40, n. 4, p. 287, doi. 10.1111/j.1399-0004.1991.tb03098.x
- By:
- Publication type:
- Article