Psychosocial Aspects of Familial Breast and Ovarian Cancer: Psychological Guidelines for Genetic Testing

por Decruyenaere, M., Evers-Kiebooms, G., Claes, E., Denayer, L., Welkenhuysen, M., Legius, E., Demyttenaere, K.
Publicado 1999

The Future of Medical Imaging in the Detection of Early Markers of Disease

por Croft, Barbara Y.
Publicado 2004

Biomarker Amplification by Serum Carrier Protein Binding

por Mehta, Arpita I., Ross, Sally, Lowenthal, Mark S., Fusaro, Vincent, Fishman, David A., Petricoin, Emanuel F., Liotta, Lance A.
Publicado 2003

C242T Polymorphism in CYBA Gene (p22(phox)) and Risk of Coronary Artery Disease in a Population of Caucasian Italians

por Nasti, Sabina, Spallarossa, Paolo, Altieri, Paola, Garibaldi, Silvano, Fabbi, Patrizia, Polito, Luisa, Bacino, Luca, Brunelli, Michele, Brunelli, Claudio, Barsotti, Antonio, Ghigliotti, Giorgio
Publicado 2006

Mutation Analysis of the BRCA1 and BRCA2 Genes in the Belgian Patient Population and Identification of a Belgian Founder Mutation BRCA1 IVS5+3A>G

por Claes, Kathleen, Machackova, Eva, De Vos, Michel, Poppe, Bruce, De Paepe, Anne, Messiaen, Ludwine
Publicado 1999

BsmI, TaqI, ApaI and FokI Polymorphisms in the Vitamin D Receptor (VDR) Gene and the Risk of Osteoporosis: A Meta-Analysis

por Zintzaras, Elias, Rodopoulou, Paraskevi, Koukoulis, George N.
Publicado 2006

Transforming Growth Factor-β and Nitrates in Epithelial Ovarian Cancer

por Khalifa, Ali, Kassim, Samar K., Ahmed, Maha I., Fayed, Salah T.
Publicado 1999

Increasing Evidence for Involvement of SV40 in Human Cancer

por Butel, Janet S.
Publicado 2001

Haplotype Analysis of Norwegian and Swedish Patients with Acute Intermittent Porphyria (AIP): Extreme Haplotype Heterogeneity for the Mutation R116W

por Tjensvoll, Kjersti, Bruland, Ove, Floderus, Ylva, Skadberg, Øyvind, Sandberg, Sverre, Apold, Jaran
Publicado 2003

Time-Resolved Fluorometry Based Sandwich Hybridisation Assay for HLA-DQA1 Typing

por Sjöroos, Minna, Ilonen, Jorma, Reijonen, Helena, Lövgren, Timo
Publicado 1998

Multiple Sclerosis Cerebrospinal Fluid Biomarkers

por Giovannoni, Gavin
Publicado 2006

Mutation-Specific Survival of Inherited Breast Cancer

por Møller, P., Borg, Å., Evans, G., Haites, N., Steel, C. M., Vasen, H., Gregory, H., Hodgson, S., Apold, J., Lalloo, F., Mæhle, L., Anderson, E., Heimdal, K., The Biomed 2 Demonstration Programme on Inherited Breast Cancer
Publicado 1999

Inherited Breast Cancer

por Nonni, Aphrodite V., Agnantis, Niki J., Kontostolis, Emmanuel, Lolis, Dimitrios
Publicado 1999

Mutation Analysis of BRCA1 and BRCA2 in Italian Hereditary and Sporadic Forms of Breast and Ovarian Cancers: Tumor Genotype-Phenotype Correlation in Breast Cancer BRCA-Mutation Car...

por Cipollini, G., Ghimenti, C., Sensi, E., Iandolo, D., Piccirilli, A., Berti, A., Naccarato, G., Viacava, P., Campani, D., Bevilacqua, G., Caligo, M. A.
Publicado 1999

Using Serial Analysis of Gene Expression to Identify Tumor Markers and Antigens

por Riggins, Gregory J.
Publicado 2001

Teaching Breast Cancer Genetics to Medical Students: Evaluation of a Computer Assister Learning (CAL) Package

por Miedzybrodzka, Z., Hamilton, N. M., Gregory, H., Milner, B., Frade, I., Sinclair, T., Mollison, J., Haites, N.
Publicado 1999

Cancer Genetics Services in the UK

por Hodgson, Shirley V.
Publicado 1999

BRCA1 and BRCA2 Gene Mutations in Breast/Ovarian Cancer Patients from Central and Southern Italy

por Ottini, Laura, D’Amico, Cristina, Noviello, Cristiana, Lauro, Salvatore, Fornarini, Giuseppe, Colantuoni, Anna, Cortesi, Enrico, Carlini, Sandro, Guadagni, Fiorella, Masala, Giovanna, Bianco, Angelo Raffaele, Contegiacomo, Alma, Palli, Domenico, Mariani-Costantini, Renato
Publicado 1999

The Role of DNA Methylation in the Development and Progression of Lung Adenocarcinoma

por Kerr, Keith M., Galler, Janice S., Hagen, Jeffrey A., Laird, Peter W., Laird-Offringa, Ite A.
Publicado 2007

Biochemical Changes in Patients with Combined Chronic Schistosomiasis and Viral Hepatitis C Infections

por Fahim, Fawzia A., Esmat, Amr Y., Hassan, Gehan K., Abdel-Bary, Abeer
Publicado 2000