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69篇 您的检索式:作者名="LASHO T"
    题名 作者 年代 出处 被引量
1JAK2 617F mutation in essential thrombocy thaemia: clincal associations and long-term prognostic relevance 显示文摘WOLANSKYI A P LASHO T L SCHWAGER S M 2005Br J Haematol2005,131,2:1
2MPL515 mutations in myeloproliferative and other myeloid disorders:a study of 1182patients显示文摘Pardanani AD Levine RL Lasho T 0,,10:1
3MPL515 mutations in myeloproliferative and other myeloid disorders: a study of 1182 patients显示文摘Pardanani AD Levine RL Lasho T 2006Blood2006,108,10:1
4Validation of two clinically useful assays for evaluation of JAK2V617F mutation in chronic myeloproliferative disorders显示文摘McClure R Mai M Lasho T 2006Leukemia2006,20,1:1
5The JAK2 tyrosine kinase mutation in myelofibrosis with myeloid metaplasia; lineage specificity and clinical correlates 显示文摘TEFFERI A LASHO T L SCHWAGER S M 2005Br J Haematol2005,131,3:1
6The JAK2 V617F activating tyrosine kinase mutation is an infrequent event in both 'atypical' myeloproliferative disorders and myelodysplastic syndromes显示文摘STEENSMA D P DEWALD G W LASHO T L 2005Blood2005,106,:1
7Clinical correlates of JAK2V617Fallele burden in es-sential thrombocythemia显示文摘KITTUR J KNUDSON R A LASHO T L 2007Cancer2007,109,:1
8MPI-515 mutations in myelo- proliferative and other myeloid disorders :a study of 1182 patients显示文摘Pardanani AD Levine RL Lasho T 2006Blood2006,108,10:1
9Validation of two clinically useful assays for evaluation of JAK2 V617F mutation in chronic myelop roliferarive disorders显示文摘McClure R.MaiM Lasho T 0,,:1
10SF3B1 mutations in primary myelofibrosis: Clinical, histopath- ology and genetic correlates among 155 patients显示文摘Lasho T L Finke C M Hanson C A 2012Leukemia2012,26,5:1
11Molecular and prognostic correlates of cytogenetic abnormalities in chronic myelomonocytic leukemia:a Mayo Clinic French Consortium Study显示文摘Wassie E A Itzykson R Lasho T L 2014American journal of hematology2014,89,12:1
12MPL515 mutations in myeloproliferative and other myeloid disorders:a study of 1182 patients显示文摘Pardanani A D Levine R L Lasho T 0,,:1
13The JAK2 V617F activating tyrosine kinase mutation is an infrequent event in both 'atypical'myeloproliferative disorders and myelodysplastic syndromes显示文摘Steensma D P Dewald G W Lasho T L 2005Blood2005,106,4:1
14Concomitantneutrophil JAK2 mutation screening and PRV-1 expres-sionanalysis in myeloproliferative disorders and secondarypolycy-thaemia显示文摘TEFFERI A SIRHAN S LASHO T L 2005Br J Haematol2005,131,2:1
15MPL515 mutations in myeloproliferative and other myeloid disorders: a study of 1 182 patients 显示文摘Pardanani AD Levine RL Lasho T 2006Blood2006,108,10:1
16MPL515 mutations in myeloproliferative and other myeloid disorders:a study of 1182 patients显示文摘Pardanani AD Levine RL Lasho T 2006Blood2006,108,10:1
17Validation of two clinically useful assays for evaluation of JAK2 V617F mutation in chronic myeloproliferative disorders显示文摘Mcclure R Mai M Lasho T 2006Leukemia2006,20,1:1
18MPL515 mutations in myeloproliferative and other myeloid disorders: a study of 1 182 patients 显示文摘Pardanani AD Levine RL Lasho T 2006Blood2006,108,10:1
19MPL515 mutations in myeloproliferative and other myeloid disorders: a study of 1182 patients 显示文摘PARDANANI A D LEVINE R L LASHO T 2006Blood2006,108,10:1
20SRSF2 mutations in primary myelofibrosis: significant clustering with IDH mutations and independent association with inferior overall and leukemia-free survival 显示文摘Lasho TL Jimma T Finke CM 2012Blood2012,120,20:1
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