Molecular Mechanisms of Fanconi Anemia /
Ahmad, Shamim I.
Molecular Mechanisms of Fanconi Anemia / by Shamim I. Ahmad, Sandra H. Kirk. - xiii, 121 páginas, recurso en línea. - Medical Intelligence Unit .
Springer eBooks
Clinical Features of Fanconi Anaemia -- The Genetic Basis of Fanconi Anemia -- The FANCA Gene and Its Products -- The FANCC Gene and Its Products -- The FANC B, E, F and G Genes and Their Products -- FANCD1/BRCA2 and FANCD2 -- The FANC Genome Surveillance Complex -- Other Proteins and Their Interactions with FA Gene Products -- Fanconi Anaemia and Oxidative Stress -- Therapy for Fanconi Anemia -- Mutational Analyses of Fanconi Anemia Genes in Japanese Patients.
Molecular Mechanisms of Fanconi Anemia will give research students a platform for further investigation, and act as a source of information regarding experimental design. Clinicians will find this title useful for its comprehensive description of Fanconi Anemia and information on the latest molecular theories underlying its causes.
9780387337760
10.1007/0387337768 doi
QH506
Molecular Mechanisms of Fanconi Anemia / by Shamim I. Ahmad, Sandra H. Kirk. - xiii, 121 páginas, recurso en línea. - Medical Intelligence Unit .
Springer eBooks
Clinical Features of Fanconi Anaemia -- The Genetic Basis of Fanconi Anemia -- The FANCA Gene and Its Products -- The FANCC Gene and Its Products -- The FANC B, E, F and G Genes and Their Products -- FANCD1/BRCA2 and FANCD2 -- The FANC Genome Surveillance Complex -- Other Proteins and Their Interactions with FA Gene Products -- Fanconi Anaemia and Oxidative Stress -- Therapy for Fanconi Anemia -- Mutational Analyses of Fanconi Anemia Genes in Japanese Patients.
Molecular Mechanisms of Fanconi Anemia will give research students a platform for further investigation, and act as a source of information regarding experimental design. Clinicians will find this title useful for its comprehensive description of Fanconi Anemia and information on the latest molecular theories underlying its causes.
9780387337760
10.1007/0387337768 doi
QH506