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NBS1
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Mutations in tumor suppressor gene NBS1 in adult patients with malignancies
2006 |
Second Faculty of Medicine
publication
Tumor supressor gene NBS1 among children patients with malignancies
2004 |
First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
publication
Mutations in Tumor Suppressor Gene NBS1 in Adult Patients with Malignancies
2006 |
First Faculty of Medicine
publication
Is Defect in Phosphorylation of Nbs1 Responsible for High Radiosensitivity of T-Lymphocyte Leukemia Cells MOLT-4?
2008 |
First Faculty of Medicine
publication
Is defect in phosphorylation of Nbs1 responsible for high radiosensitivity of T-lymphocyte leukemia cells MOLT-4?
2008 |
First Faculty of Medicine
publication
Increased Risk of Malignancies in Heterozygotes in Families of Patients with Nijmegen Breakage Syndrome
2006 |
Second Faculty of Medicine
publication
Nijmegen Breakage Syndrome (NBS)
1999 |
Second Faculty of Medicine
publication
Is defect in phosphorylation of Nbs1 responsible for high radiosensitivity of T-lymphocyte leukemia cells MOLT-4?
2008 |
Faculty of Medicine in Hradec Králové
publication
Nijmegen breakage syndrome (NBS) with neurological abnormalities and without chromosomal instability
2006 |
Second Faculty of Medicine
publication
Nijmegen breakage syndrome in Slovakia
2004 |
Second Faculty of Medicine
publication
Cancer incidence in Nijmegen breakage syndrome is modulated by the amount of a variant NBS protein
2007 |
Second Faculty of Medicine
publication
Germline mutations 657del5 and 643C > T (R215W) in NBN are not likely to be associated with increased risk of breast cancer in Czech women
2012 |
First Faculty of Medicine
publication
The clinical importance of a genetic analysis of moderate-risk cancer susceptibility genes in breast and other cancer patients from the Czech Republic
2012 |
First Faculty of Medicine
publication
Nijmegen Breakage Syndrome - neglected primary immunodeficiency
2012 |
Second Faculty of Medicine
publication
Cancer risk of heterozygotes with the NBN founder mutation
2007 |
Second Faculty of Medicine
publication
The Slavic NBN Founder Mutation: A Role for Reproductive Fitness?
2016 |
First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
publication
Clinical ascertainment of Nijmegen breakage syndrome (NBS) and prevalence of the major mutation, 657de15, in three Slav populations
2000 |
Second Faculty of Medicine
publication
Mitoxantrone in Combination with a DNA-PK Inhibitor: Possible Therapy of Promyelocytic Leukaemia Resistant Forms
2011 |
Faculty of Medicine in Hradec Králové
publication
Nijmegen breakage syndrome in 13% of age-matched Czech children with primary microcephaly
2004 |
Second Faculty of Medicine
publication
Extreme variation in apoptosis capacity amongst lymphoid cells of Nijmegen breakage syndrome patients
2008 |
Second Faculty of Medicine
publication
Women at high risk of breast cancer: Molecular characteristics, clinical presentation and management
2016 |
First Faculty of Medicine