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Volumn 31, Issue 4, 2007, Pages 477-482

Hb Niigata [β1(Na1)Val→Leu] in a Romanian individual resulting from another nucleotide substitution than that found in the Japanese

Author keywords

Allelic heterogeneity; Hb Niigata; Posttranslational modification

Indexed keywords

HEMOGLOBIN BETA CHAIN; HEMOGLOBIN NIIGATA; HEMOGLOBIN VARIANT; LEUCINE; METHIONINE; UNCLASSIFIED DRUG; VALINE; GLOBIN;

EID: 36248957657     PISSN: 03630269     EISSN: 1532432X     Source Type: Journal    
DOI: 10.1080/03630260701587885     Document Type: Article
Times cited : (3)

References (16)
  • 1
    • 0037462954 scopus 로고    scopus 로고
    • N-terminal acetyltransferases and sequence requirements for N-terminal acetylation of eukaryotic proteins
    • Polevoda B, Sherman F. N-terminal acetyltransferases and sequence requirements for N-terminal acetylation of eukaryotic proteins. J Mol Biol 2003; 325(4):595-622.
    • (2003) J Mol Biol , vol.325 , Issue.4 , pp. 595-622
    • Polevoda, B.1    Sherman, F.2
  • 4
    • 2242432089 scopus 로고
    • Amino-terminal processing of proteins: Hemoglobin South Florida, a variant with retention of initiator methionine and N α-acetylation
    • Boissel JP, Kasper TJ, Shah SC, Malone JI, Bunn HF. Amino-terminal processing of proteins: Hemoglobin South Florida, a variant with retention of initiator methionine and N α-acetylation. Proc Natl Acad Sci USA 1985; 82(24):8448-8452.
    • (1985) Proc Natl Acad Sci USA , vol.82 , Issue.24 , pp. 8448-8452
    • Boissel, J.P.1    Kasper, T.J.2    Shah, S.C.3    Malone, J.I.4    Bunn, H.F.5
  • 5
    • 34547161963 scopus 로고    scopus 로고
    • 3.7 thalassemia deletion. Hemoglobin 2007; 31(3):313-323.
    • 3.7 thalassemia deletion. Hemoglobin 2007; 31(3):313-323.
  • 7
    • 7144264399 scopus 로고    scopus 로고
    • A nondiabetic case of hemoglobin variant (Hb Niigata) with inappropriately high and low HbA1c titers detected by different methods
    • Watanabe T, Kato K, Yamada D, Midorikawa S, Sato W, Shiga M, Otsuka Y, Miura M, Harano K, Harano T. A nondiabetic case of hemoglobin variant (Hb Niigata) with inappropriately high and low HbA1c titers detected by different methods. Clin Chem 1998; 44(7):1562-1564.
    • (1998) Clin Chem , vol.44 , Issue.7 , pp. 1562-1564
    • Watanabe, T.1    Kato, K.2    Yamada, D.3    Midorikawa, S.4    Sato, W.5    Shiga, M.6    Otsuka, Y.7    Miura, M.8    Harano, K.9    Harano, T.10
  • 9
    • 0012347434 scopus 로고
    • Hemoglobin Long Island is caused by a single mutation (adenine to cytosine) resulting in a failure to cleave amino-terminal methionine
    • Prchal JT, Cashman DP, Kan YW. Hemoglobin Long Island is caused by a single mutation (adenine to cytosine) resulting in a failure to cleave amino-terminal methionine. Proc Natl Acad Sci USA 1986; 83(1):24-27.
    • (1986) Proc Natl Acad Sci USA , vol.83 , Issue.1 , pp. 24-27
    • Prchal, J.T.1    Cashman, D.P.2    Kan, Y.W.3
  • 10
    • 0036190154 scopus 로고    scopus 로고
    • HbVar: A relational database of human hemoglobin variants and thalassemia mutations at the globin gene server
    • Hardison RC, Chui DHK, Giardine B, Riemer C, Patrinos GP, Anagnou N, Miller W, Wajcman H. HbVar: A relational database of human hemoglobin variants and thalassemia mutations at the globin gene server. Hum Mutat 2002; 19(3):225-233 (http://globin.cse.psu.edu).
    • (2002) Hum Mutat , vol.19 , Issue.3 , pp. 225-233
    • Hardison, R.C.1    Chui, D.H.K.2    Giardine, B.3    Riemer, C.4    Patrinos, G.P.5    Anagnou, N.6    Miller, W.7    Wajcman, H.8
  • 11
    • 0347125141 scopus 로고    scopus 로고
    • Patrinos GP, Giardine B, Riemer C, Miller W, Chui DHK, Anagnou NP, Wajcman H, Hardison RC. Improvements in the HbVar database of human hemoglobin variants and thalassemia mutations for population and sequence variation studies. Nucleic Acids Res 2004; 32(Database issue):D537-D541.
    • Patrinos GP, Giardine B, Riemer C, Miller W, Chui DHK, Anagnou NP, Wajcman H, Hardison RC. Improvements in the HbVar database of human hemoglobin variants and thalassemia mutations for population and sequence variation studies. Nucleic Acids Res 2004; 32(Database issue):D537-D541.
  • 12
    • 0026548860 scopus 로고
    • Hb Kodaira [β146(HC3)His→Gln]: A new β chain variant with an amino acid substitution at the C-terminus
    • Harano T, Harano K, Kushida Y, Imai K, Nishinakamura R, Matsunaga T. Hb Kodaira [β146(HC3)His→Gln]: a new β chain variant with an amino acid substitution at the C-terminus. Hemoglobin 1992; 16(1&2):85-91.
    • (1992) Hemoglobin , vol.16 , Issue.1-2 , pp. 85-91
    • Harano, T.1    Harano, K.2    Kushida, Y.3    Imai, K.4    Nishinakamura, R.5    Matsunaga, T.6
  • 13
    • 0036063528 scopus 로고    scopus 로고
    • So CC, Ma SK, Law KM, Chan AY, Chan LC, Wong KF. Hb Kodaira II: a high oxygen affinity variant with a novel mutation in the β-globin gene and phenotypic identity to Hb Kodaira. Hemoglobin 2002; 26(2):205-207.
    • So CC, Ma SK, Law KM, Chan AY, Chan LC, Wong KF. Hb Kodaira II: a high oxygen affinity variant with a novel mutation in the β-globin gene and phenotypic identity to Hb Kodaira. Hemoglobin 2002; 26(2):205-207.
  • 16
    • 0033987736 scopus 로고    scopus 로고
    • Mutation nomenclature extensions and suggestions to describe complex mutations: A discussion
    • den Dunnen JT, Antonarakis SE. Mutation nomenclature extensions and suggestions to describe complex mutations: a discussion. Hum Mutat 2000; 15(1):7-12.
    • (2000) Hum Mutat , vol.15 , Issue.1 , pp. 7-12
    • den Dunnen, J.T.1    Antonarakis, S.E.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.