✦ LIBER ✦

Screening of JAK2 V617F mutation in multiple myeloma

✍ Scribed by Fiorini, A; Farina, G; Reddiconto, G; Palladino, M; Rossi, E; Za, T; Laurenti, L; Giammarco, S; Chiusolo, P; Leone, G

Book ID: 110056848
Publisher: Nature Publishing Group
Year: 2006
Tongue: English
Weight: 67 KB
Volume: 20
Category: Article
ISSN: 0887-6924
DOI: 10.1038/sj.leu.2404332

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Reply to ‘Absence of JAK-2 (Val617Phe) p

Reply to ‘Absence of JAK-2 (Val617Phe) point mutations in multiple myeloma’ by Dr Qin Huang et al. referred to ‘Screening of JAK2 V617F mutation in multiple myeloma’ from Fiorini A et al. published in Leukemia 2006, October 20

✍ Fiorini, A; Farina, G; Reddiconto, G; Palladino, M; Rossi, E; Za, T; Laurenti, L 📂 Article 📅 2007 🏛 Nature Publishing Group 🌐 English ⚖ 79 KB

Absence of JAK-2V617F point mutations in

Absence of JAK-2V617F point mutations in multiple myeloma

✍ Huang, Q; Li, X; Chen, W; Weiss, L M 📂 Article 📅 2007 🏛 Nature Publishing Group 🌐 English ⚖ 110 KB

JAK2 (V617F) mutation in healthy individ

JAK2 (V617F) mutation in healthy individuals

✍ Francesco Passamonti; Elisa Rumi; Daniela Pietra; Mario Lazzarino; Mario Cazzola 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 436 KB

The JAK2V617F mutation and thrombosis

✍ S. K. Austin; J. R. Lambert 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 132 KB

JAK2-V617F mutation in cerebral venous t

JAK2-V617F mutation in cerebral venous thrombosis

✍ K. KOOPMAN; A. B. MULDER; J. DE KEYSER; G. J. LUIJCKX; J. VAN DER MEER 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 80 KB

The V617F JAK2 mutation and the myelopro

The V617F JAK2 mutation and the myeloproliferative disorders

✍ Melanie J Percy; Mary Frances McMullin 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 70 KB

## Abstract The discovery this year of a single mutation in the Janus Kinase (__JAK__)‐2 gene in a high percentage of cases of polycythaemia vera (PV), essential thrombocythaemia (ET) and myelofibrosis suggests that it maybe the underlying molecular mechanism for these disorders. Different approach