Detalles de la búsqueda
1.
Identification of Spliceogenic Variants beyond Canonical GT-AG Splice Sites in Hereditary Cancer Genes.
Int J Mol Sci;
23(13)2022 Jul 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-35806449
2.
Genetic testing results in Slovenian male breast cancer cohort indicate the BRCA2 7806-2A > G founder variant could be associated with higher male breast cancer risk.
Breast Cancer Res Treat;
188(3): 811-820, 2021 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-33891299
3.
Bilateral Disease Common Among Slovenian CHEK2-Positive Breast Cancer Patients.
Ann Surg Oncol;
28(5): 2561-2570, 2021 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-33030641
4.
An interesting case of likely BRCA2 related bilateral breast cancer with metastasis in the fimbrial part of fallopian tube.
Hered Cancer Clin Pract;
18: 7, 2020.
Artículo
en Inglés
| MEDLINE | ID: mdl-32206145
5.
Cytology material is equivalent to tumor tissue in determining mutations of BRCA 1/2 genes in patients with tubo-ovarian high grade serous carcinoma.
BMC Cancer;
19(1): 296, 2019 Apr 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-30940100
6.
Genetic Counselling, BRCA1/2 Status and Clinico-pathologic Characteristics of Patients with Ovarian Cancer before 50 Years of Age.
Radiol Oncol;
51(2): 187-194, 2017 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-28740454
7.
A Population-Based Study of Patients With Small Cell Carcinoma of the Ovary, Hypercalcemic Type, Encompassing a 30-Year Period.
Arch Pathol Lab Med;
148(3): 299-309, 2024 Mar 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-37270804
8.
Cytopathological assessment is an accurate method for identifying immunophenotypic features and BRCA1/2 mutations of high-grade serous carcinoma from ascites.
Cancer Cytopathol;
131(3): 188-197, 2023 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-36399410
9.
KRAS rs61764370 is associated with HER2-overexpressed and poorly-differentiated breast cancer in hormone replacement therapy users: a case control study.
BMC Cancer;
12: 105, 2012 Mar 22.
Artículo
en Inglés
| MEDLINE | ID: mdl-22436609
10.
Correlation of treatment outcome in sanger/RTqPCR KIT/PDGFRA wildtype metastatic gastrointestinal stromal tumors with nextgeneration sequencing results: A singlecenter report.
Oncol Rep;
48(3)2022 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-35904169
11.
BAP1-defficient breast cancer in a patient with BAP1 cancer syndrome.
Breast Cancer;
29(5): 921-927, 2022 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-35381901
12.
Real-World Data on Detection of Germline and Somatic Pathogenic/Likely Pathogenic Variants in BRCA1/2 and Other Susceptibility Genes in Ovarian Cancer Patients Using Next Generation Sequencing.
Cancers (Basel);
14(6)2022 Mar 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-35326583
13.
The occurrence of germline BRCA1 and BRCA2 sequence alterations in Slovenian population.
BMC Med Genet;
12: 9, 2011 Jan 14.
Artículo
en Inglés
| MEDLINE | ID: mdl-21232165
14.
New Approach for Detection of Normal Alternative Splicing Events and Aberrant Spliceogenic Transcripts with Long-Range PCR and Deep RNA Sequencing.
Biology (Basel);
10(8)2021 Jul 23.
Artículo
en Inglés
| MEDLINE | ID: mdl-34439939
15.
Tumor vaccine composed of C-class CpG oligodeoxynucleotides and irradiated tumor cells induces long-term antitumor immunity.
BMC Immunol;
11: 45, 2010 Sep 13.
Artículo
en Inglés
| MEDLINE | ID: mdl-20836870
16.
The prevalence of occult ovarian cancer in the series of 155 consequently operated high risk asymptomatic patients - Slovenian population based study.
Radiol Oncol;
54(2): 180-186, 2020 May 28.
Artículo
en Inglés
| MEDLINE | ID: mdl-32463390
17.
Risk factors for the development of high-grade dysplasia and carcinoma in patients with laryngeal squamous cell papillomas: Large retrospective cohort study.
Head Neck;
2020 Dec 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-33289174
18.
Mutational spectrum and classification of novel mutations in patients with metastatic gastrointestinal stromal tumours.
Int J Oncol;
56(6): 1468-1478, 2020 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-32236636
19.
A Novel Germline MLH1 In-Frame Deletion in a Slovenian Lynch Syndrome Family Associated with Uncommon Isolated PMS2 Loss in Tumor Tissue.
Genes (Basel);
11(3)2020 03 18.
Artículo
en Inglés
| MEDLINE | ID: mdl-32197529
20.
Two Novel NF1 Pathogenic Variants Causing the Creation of a New Splice Site in Patients With Neurofibromatosis Type I.
Front Genet;
10: 762, 2019.
Artículo
en Inglés
| MEDLINE | ID: mdl-31507634