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Myeloid Leukemia
Myeloid Leukemia
Knygos.lt klubas Knygos.lt nariams
167,57 €
-30%
Įprastai
239,39 €
  • Išsiųsime per 12–18 d.d.
A panel of internationally recognized research scientists and clinical investigators brings together a diverse collection of readily reproducible methods for identifying and quantifying a large number of specific genetic abnormalities associated with the broad spectrum of myeloid malignancies. Highlights include techniques for the detection of BCR-ABL mutations and resistance to imatinib mesylate, detection of the FIP1L1-PDGFRA fusion in idiopathic hypereosinophilic syndrome and chronic eosinop…
  • Leidėjas:
  • Metai: 2005
  • Puslapiai: 306
  • ISBN-10: 1588294854
  • ISBN-13: 9781588294852
  • Formatas: 17.7 x 23.7 x 2.7 cm, kieti viršeliai
  • Kalba: Anglų

Myeloid Leukemia (el. knyga) (skaityta knyga) | knygos.lt

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A panel of internationally recognized research scientists and clinical investigators brings together a diverse collection of readily reproducible methods for identifying and quantifying a large number of specific genetic abnormalities associated with the broad spectrum of myeloid malignancies. Highlights include techniques for the detection of BCR-ABL mutations and resistance to imatinib mesylate, detection of the FIP1L1-PDGFRA fusion in idiopathic hypereosinophilic syndrome and chronic eosinophilic leukemia, classification of AML by DNA-oligonucleotide microarrays, and detection of the V617F JAK2 mutation in myeloproliferative disorders. In addition to gene rearrangments, other prognostically relevant molecular lesions such as FLT3 mutations and WT-1 overexpression are covered.

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  • Leidėjas:
  • Metai: 2005
  • Puslapiai: 306
  • ISBN-10: 1588294854
  • ISBN-13: 9781588294852
  • Formatas: 17.7 x 23.7 x 2.7 cm, kieti viršeliai
  • Kalba: Anglų

A panel of internationally recognized research scientists and clinical investigators brings together a diverse collection of readily reproducible methods for identifying and quantifying a large number of specific genetic abnormalities associated with the broad spectrum of myeloid malignancies. Highlights include techniques for the detection of BCR-ABL mutations and resistance to imatinib mesylate, detection of the FIP1L1-PDGFRA fusion in idiopathic hypereosinophilic syndrome and chronic eosinophilic leukemia, classification of AML by DNA-oligonucleotide microarrays, and detection of the V617F JAK2 mutation in myeloproliferative disorders. In addition to gene rearrangments, other prognostically relevant molecular lesions such as FLT3 mutations and WT-1 overexpression are covered.

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