SCOPUS 정보 검색 플랫폼

Blood

Volumn 115, Issue 16, 2010, Pages 3415-3416

Role of GATA-1s in early hematopoiesis and differences between alternative splicing in human and murine GATA-1

(5) Halsey, Christina a Tunstall, Oliver b Gibson, Brenda c Roberts, Irene b Graham, Gerard a

a UNIVERSITY OF GLASGOW (United Kingdom)

b IMPERIAL COLLEGE LONDON (United Kingdom)

c ROYAL HOSPITAL FOR SICK CHILDREN (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

TRANSCRIPTION FACTOR GATA 1;

ALTERNATIVE RNA SPLICING; EXON; HEMATOPOIESIS; IMMUNOHISTOCHEMISTRY; LETTER; MUTATION; MYELOPROLIFERATIVE DISORDER; PRIORITY JOURNAL; PROTEIN FUNCTION;

EID: 77951444724 PISSN: 00064971 EISSN: 15280020 Source Type: Journal
DOI: 10.1182/blood-2010-02-267930 Document Type: Letter

Times cited : (7)

References (5)

1
- 70449502130
- New GATA1 mutation in codon 2 leads to the earliest known premature stop codon in transient myeloproliferative disorder
- Hoeller S, Bihl MP, Tzankov A, Kuehne T, Potthoff C, Bruder E. New GATA1 mutation in codon 2 leads to the earliest known premature stop codon in transient myeloproliferative disorder. Blood. 2009;114(17):3717-3718.
- (2009) Blood , vol.114 , Issue.17 , pp. 3717-3718
- Hoeller, S.¹ Bihl, M.P.² Tzankov, A.³ Kuehne, T.⁴ Potthoff, C.⁵ Bruder, E.⁶

2
- 0042243593
- Mutations in exon 2 of GATA1 are early events in megakaryocytic malignancies associated with trisomy 21
- DOI 10.1182/blood-2002-11-3599
- Rainis L, Bercovich D, Strehl S, et al. Mutations in exon 2 of GATA1 are early events in megakaryocytic malignancies associated with trisomy 21. Blood. 2003;102(3):981-986. (Pubitemid 36917793)
- (2003) Blood , vol.102 , Issue.3 , pp. 981-986
- Rainis, L.¹ Bercovich, D.² Strehl, S.³ Teigler-Schlegel, A.⁴ Stark, B.⁵ Trka, J.⁶ Amariglio, N.⁷ Biondi, A.⁸ Muler, I.⁹ Rechavi, G.¹⁰ Kempski, H.¹¹ Haas, O.A.¹² Izraeli, S.¹³

3
- 12144287045
- Natural history of GATA1 mutations in Down syndrome
- DOI 10.1182/blood-2003-10-3383
- Ahmed M, Sternberg A, Hall G, et al. Natural history of GATA1 mutations in Down syndrome. Blood. 2004;103(7):2480-2489. (Pubitemid 38392997)
- (2004) Blood , vol.103 , Issue.7 , pp. 2480-2489
- Ahmed, M.¹ Sternberg, A.² Hall, G.³ Thomas, A.⁴ Smith, O.⁵ O'Marcaigh, A.⁶ Wynn, R.⁷ Stevens, R.⁸ Addison, M.⁹ King, D.¹⁰ Stewart, B.¹¹ Gibson, B.¹² Roberts, I.¹³ Vyas, P.¹⁴

4
- 0141889275
- Frequent mutations in the GATA-1 gene in the transient myeloproliferative disorder of Down syndrome
- DOI 10.1182/blood-2003-02-0390
- Xu G, Nagano M, Kanezaki R, et al. Frequent mutations in the GATA-1 gene in the transient myeloproliferative disorder of Down syndrome. Blood. 2003; 102(8):2960-2968. (Pubitemid 37248871)
- (2003) Blood , vol.102 , Issue.8 , pp. 2960-2968
- Xu, G.¹ Nagano, M.² Kanezaki, R.³ Toki, T.⁴ Hayashi, Y.⁵ Taketani, T.⁶ Taki, T.⁷ Mitui, T.⁸ Koike, K.⁹ Kato, K.¹⁰ Imaizumi, M.¹¹ Sekine, I.¹² Ikeda, Y.¹³ Hanada, R.¹⁴ Sako, M.¹⁵ Kudo, K.¹⁶ Kojima, S.¹⁷ Ohneda, O.¹⁸ Yamamoto, M.¹⁹ Ito, E.²⁰ more..

5
- 0029558618
- Alternative translation initiation site usage results in two functionally distinct forms of the GATA-1 transcription factor
- Calligaris R, Bottardi S, Cogoi S, Apezteguia I, Santoro C. Alternative translation initiation site usage results in two functionally distinct forms of the GATA-1 transcription factor. Proc Natl Acad Sci U S A. 1995;92(25):11598- 11602.
- (1995) Proc Natl Acad Sci U S A , vol.92 , Issue.25 , pp. 11598-11602
- Calligaris, R.¹ Bottardi, S.² Cogoi, S.³ Apezteguia, I.⁴ Santoro, C.⁵

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.