المؤلفون: van Twest, Sylvie, Deans, Andrew

المساهمون: St Vincent's Institute of Medical Research, 9 Princes St, Fitzroy VIC 3065, Australia

مصطلحات موضوعية: FANCB, Fanconi Anemia, Ubiquitination, VACTERL-H, Cancer pre-disposition, Chromosome X, Genes Section, Amino Acid Sequence, Chromatography, High Pressure Liquid, DNA-Binding Proteins/chemistry/genetics/metabolism, Dimerization, Fanconi Anemia Complementation Group D2 Protein/chemistry/genetics/*metabolism, Fanconi Anemia Complementation Group Proteins/chemistry/genetics/*metabolism, Humans, Mass Spectrometry, Microscopy, Electron, Protein Multimerization, Protein Structure, Tertiary, Substrate Specificity, Cell Line, DNA/genetics/metabolism, DNA-Binding Proteins/metabolism, Fanconi Anemia/genetics/*metabolism, Fanconi Anemia Complementation Group A Protein/metabolism, Fanconi Anemia Complementation Group C Protein/metabolism, Fanconi Anemia Complementation Group D2 Protein/genetics/*metabolism, Fanconi Anemia Complementation Group E Protein/metabolism

العلاقة: Atlas of Genetics and Cytogenetics in Oncology and Haematology; http://AtlasGeneticsOncology.org/Genes/FANCBID49864chXp22.htmlTest; Sylvie, van Twest; Andrew, Deans. FANCB (FA complementation group B). Atlas of Genetics and Cytogenetics in Oncology and Haematology, 2020, 1, p. 18-21; http://hdl.handle.net/2042/70644Test; https://doi.org/10.4267/2042/70644Test

الإتاحة: https://doi.org/10.4267/2042/70644Test
http://hdl.handle.net/2042/70644Test

المؤلفون: Hoeijmakers, J.H.J. (Jan), Bootsma, D. (Dirk)

المصدر: Nature Genetics vol. 1 no. 5, pp. 313-314

مصطلحات موضوعية: Amino Acid Sequence, Ataxia Telangiectasia/genetics, Bloom Syndrome/genetics, DNA Damage, DNA Repair/*genetics, Fanconi Anemia/genetics, Genes, Recessive, Human, Point Mutation, Sister Chromatid Exchange, Xeroderma Pigmentosum/genetics

وصف الملف: application/pdf

العلاقة: http://repub.eur.nl/pub/3039Test; urn:hdl:1765/3039

الإتاحة: https://doi.org/10.1038/ng0892-313Test
http://repub.eur.nl/pub/3039Test