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1.
Detection of Germline Variants in 450 Breast/Ovarian Cancer Families with a Multi-Gene Panel Including Coding and Regulatory Regions.
Int J Mol Sci
; 22(14)2021 Jul 19.
Artículo
en Inglés
| MEDLINE | ID: mdl-34299313
2.
Characterization of the rs2802292 SNP identifies FOXO3A as a modifier locus predicting cancer risk in patients with PJS and PHTS hamartomatous polyposis syndromes.
BMC Cancer
; 14: 661, 2014 Sep 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-25208626
3.
Remote vs in-person BRCA1/2 non-carriers test disclosure: patients' choice during Covid-19 pandemic restriction.
Fam Cancer
; 22(1): 43-48, 2023 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-35867288
4.
SIUrO best practice recommendations to optimize BRCA 1/2 gene testing from DNA extracted from bone biopsy in mCRPC patients (BRCA Optimal Bone Biopsy Procedure: BOP).
Virchows Arch
; 483(5): 579-589, 2023 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-37794204
5.
Spectrum of Germline Pathogenic Variants in BRCA1/2 Genes in the Apulian Southern Italy Population: Geographic Distribution and Evidence for Targeted Genetic Testing.
Cancers (Basel)
; 13(18)2021 Sep 21.
Artículo
en Inglés
| MEDLINE | ID: mdl-34572941
6.
Blood Arsenic Levels as a Marker of Breast Cancer Risk among BRCA1 Carriers.
Cancers (Basel)
; 13(13)2021 Jul 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-34283078
7.
Oncological genetic counseling (OGC) for high-risk hereditary cancer: what can hospital anxiety and depression scale (HADs) tell us?
J BUON
; 25(1): 566-573, 2020.
Artículo
en Inglés
| MEDLINE | ID: mdl-32277684
8.
Somatic BRCA Mutation in a Cholangiocarcinoma Patient for HBOC Syndrome Detection.
Front Oncol
; 10: 1292, 2020.
Artículo
en Inglés
| MEDLINE | ID: mdl-32903564
9.
The Role of Circulating Adiponectin and SNP276G>T at ADIPOQ Gene in BRCA-mutant Women.
Cancer Genomics Proteomics
; 17(3): 301-307, 2020.
Artículo
en Inglés
| MEDLINE | ID: mdl-32345671
10.
Accurate Classification of NF1 Gene Variants in 84 Italian Patients with Neurofibromatosis Type 1.
Genes (Basel)
; 9(4)2018 Apr 17.
Artículo
en Inglés
| MEDLINE | ID: mdl-29673180
11.
Two novel cases of compound heterozygous mutations in mitofusin2: Finding out the inheritance.
Neuromuscul Disord
; 27(4): 377-381, 2017 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-28215760
12.
Molecular and Functional Characterization of Three Different Postzygotic Mutations in PIK3CA-Related Overgrowth Spectrum (PROS) Patients: Effects on PI3K/AKT/mTOR Signaling and Sensitivity to PIK3 Inhibitors.
PLoS One
; 10(4): e0123092, 2015.
Artículo
en Inglés
| MEDLINE | ID: mdl-25915946
13.
A rare MSH2 mutation causes defective binding to hMSH6, normal hMSH2 staining, and loss of hMSH6 at advanced cancer stage.
Hum Pathol
; 45(10): 2162-7, 2014 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-25106712
14.
Survey of KRAS, BRAF and PIK3CA mutational status in 209 consecutive Italian colorectal cancer patients.
Int J Biol Markers
; 27(4): e366-74, 2012 Dec 27.
Artículo
en Inglés
| MEDLINE | ID: mdl-23125007
15.
Identification and surveillance of 19 Lynch syndrome families in southern Italy: report of six novel germline mutations and a common founder mutation.
Fam Cancer
; 10(2): 285-95, 2011 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-21286823
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