SCOPUS 정보 검색 플랫폼

Blood

Volumn 113, Issue 23, 2009, Pages 5696-5697

Adding WT1 to childhood AML alphabet soup

(1) Brown, Patrick a

a JOHNS HOPKINS UNIVERSITY (United States)

Author keywords

[No Author keywords available]

Indexed keywords

WT1 PROTEIN;

ACUTE MYELOBLASTIC LEUKEMIA; CANCER PATIENT; CHILDHOOD LEUKEMIA; FRAMESHIFT MUTATION; GENE EXPRESSION; HETEROZYGOSITY LOSS; HUMAN; NOTE; ONCOGENE; PRIORITY JOURNAL; PROGNOSIS; WT1 GENE;

EID: 70449339917 PISSN: 00064971 EISSN: 15280020 Source Type: Journal
DOI: 10.1182/blood-2009-03-207282 Document Type: Note

Times cited : (4)

References (5)

1
- 33845254595
- Clinical implications of FLT3 mutations in pediatric AML
- DOI 10.1182/blood-2006-03-009233
- Meshinchi S, Alonzo TA, Stirewalt DL, et al. Clinical implications of FLT3 mutations in pediatric AML. Blood. 2006;108:3654-3661. (Pubitemid 44864541)
- (2006) Blood , vol.108 , Issue.12 , pp. 3654-3661
- Meshinchi, S.¹ Alonzo, T.A.² Stirewalt, D.L.³ Zwaan, M.⁴ Zimmerman, M.⁵ Reinhardt, D.⁶ Kaspers, G.J.L.⁷ Heerema, N.A.⁸ Gerbing, R.⁹ Lange, B.J.¹⁰ Radich, J.P.¹¹

2
- 4444342401
- Pediatric AML primary samples with FLT3/ITD mutations are preferentially killed by FLT3 inhibition
- DOI 10.1182/blood-2004-03-1034
- Brown P, Meshinchi S, Levis M, et al. Pediatric AML primary samples with FLT3/ITD mutations are preferentially killed by FLT3 inhibition. Blood. 2004;104:1841-1849. (Pubitemid 39202295)
- (2004) Blood , vol.104 , Issue.6 , pp. 1841-1849
- Brown, P.¹ Meshinchi, S.² Levis, M.³ Alonzo, T.A.⁴ Gerbing, R.⁵ Lange, B.⁶ Arceci, R.⁷ Small, D.⁸

3
- 34547954572
- The incidence and clinical significance of nucleophosmin mutations in childhood AML
- DOI 10.1182/blood-2007-02-076604
- Brown P, McIntyre E, Rau R, et al. The incidence and clinical significance of nucleophosmin mutations in childhood AML. Blood. 2007;110:979-985. (Pubitemid 47267437)
- (2007) Blood , vol.110 , Issue.3 , pp. 979-985
- Brown, P.¹ McIntyre, E.² Rau, R.³ Meshinchi, S.⁴ Lacayo, N.⁵ Dahl, G.⁶ Alonzo, T.A.⁷ Chang, M.⁸ Arceci, R.J.⁹ Small, D.¹⁰

4
- 15044356744
- CEBPalpha mutations in childhood acute myeloid leukemia
- DOI 10.1038/sj.leu.2403608
- Liang DC, Shih LY, Huang CF, et al. CEBPalpha mutations in childhood acute myeloid leukemia. Leukemia. 2005;19:410-414. (Pubitemid 40403318)
- (2005) Leukemia , vol.19 , Issue.3 , pp. 410-414
- Liang, D.-C.¹ Shih, L.-Y.² Huang, C.-F.³ Hung, I.-J.⁴ Yang, C.-P.⁵ Liu, H.-C.⁶ Jaing, T.-H.⁷ Wang, L.-Y.⁸ Chang, W.-H.⁹

5
- 67651096058
- Clinical relevance of Wilms tumor 1 gene mutations in childhood acute myeloid leukemia
- Hollink IHIM, van den Heuvel-Eibrink MM, Zimmermann M, et al. Clinical relevance of Wilms tumor 1 gene mutations in childhood acute myeloid leukemia. Blood. 2009;113:5951-5960.
- (2009) Blood , vol.113 , pp. 5951-5960
- Hollink, I.H.I.M.¹ Van Den Heuvel-Eibrink, M.M.² Zimmermann, M.³

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.