Search results

• 2006

  Presence of JAK2 V617F tyrosine kinase mutation as a myeloid-lineage-specific mutation in chronic neutrophilic leukaemia

  Lea, N. C., Lim, Z., Westwood, N. B., Arno, M. J., Gaken, J., Mohamedali, A. & Mufti, G. J., Jul 2006, In: Leukemia. 20, 7, p. 1324 - 1326 3 p.

  Research output: Contribution to journal › Letter › peer-review
  21 Citations (Scopus)

• The JAK2 V617F mutation identifies a subgroup of MDS patients with isolated deletion 5q and a proliferative bone marrow

  Ingram, W., Lea, N. C., Cervera, J., Germing, U., Fenaux, P., Cassinat, B., Kiladjian, J. J., Varkonyi, J., Antunovic, P., Westwood, N. B., Arno, M. J., Mohamedali, A., Gaken, J., Kontou, T., Czepulkowski, B. H., Twine, N. A., Tamaska, J., Csomer, J., Benedek, S. & Gattermann, N. & 5 others, Zipperer, E., Giagounidis, A., Garcia-Casado, Z., Sanz, G. & Mufti, G. J., Jul 2006, In: Leukemia. 20, 7, p. 1319 - 1321 3 p.

  Research output: Contribution to journal › Letter › peer-review
  96 Citations (Scopus)

• The JAK2 V617F mutation is rare in RARS but common in RARS-T

  Ceesay, M. M., Lea, N. C., Ingram, W., Westwood, N. B., Gaken, J., Mohamedali, A., Cervera, J., Germing, U., Gallermann, N., Giagounidis, A., Garcia-Casado, Z., Sanz, G. & Mufti, G. J., Nov 2006, In: Leukemia. 20, 11, p. 2060 - 2061 2 p.

  Research output: Contribution to journal › Letter › peer-review
  71 Citations (Scopus)