-
1
-
-
0037462954
-
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
-
2
-
-
0026627813
-
Hemoglobin Thionville. An α-chain variant with a substitution of a glutamate for valine at NA-1 and having an acetylated methionine NH2 terminus
-
Vasseur C, Blouquit Y, Kister J, Prome D, Kavanaugh JS, Rogers PH, Guillemin C, Arnone A, Galacteros F, Poyart C, Rosa J, Wajcman H. Hemoglobin Thionville. An α-chain variant with a substitution of a glutamate for valine at NA-1 and having an acetylated methionine NH2 terminus. J Biol Chem 1992; 267(18):12682-12691.
-
(1992)
J Biol Chem
, vol.267
, Issue.18
, pp. 12682-12691
-
-
Vasseur, C.1
Blouquit, Y.2
Kister, J.3
Prome, D.4
Kavanaugh, J.S.5
Rogers, P.H.6
Guillemin, C.7
Arnone, A.8
Galacteros, F.9
Poyart, C.10
Rosa, J.11
Wajcman, H.12
-
3
-
-
0021931068
-
2[X-N-Met-1(NA1) Val→Glu]; a new β chain abnormal hemoglobin observed in a Qatari female
-
2[X-N-Met-1(NA1) Val→Glu]; a new β chain abnormal hemoglobin observed in a Qatari female. Biochim Biophys Acta 1985; 831(2):257-260.
-
(1985)
Biochim Biophys Acta
, vol.831
, Issue.2
, pp. 257-260
-
-
Kamel, K.1
El-Najjar, A.2
Webber, B.B.3
Chen, S.S.4
Wilson, J.B.5
Kutlar, A.6
Huisman, T.H.J.7
-
4
-
-
2242432089
-
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
-
-
3.7 thalassemia deletion. Hemoglobin 2007; 31(3):313-323.
-
3.7 thalassemia deletion. Hemoglobin 2007; 31(3):313-323.
-
-
-
-
6
-
-
0030938726
-
Hb Niigata [β1(NA1)Val→Leu]: The fifth variant with retention of the initiator methionine and partial acetylation
-
Ohba Y, Hattori Y, Sakata S, Yamashiro Y, Okayama N, Hirano T, Nakanishi T, Miyazaki A, Shimizu A. Hb Niigata [β1(NA1)Val→Leu]: the fifth variant with retention of the initiator methionine and partial acetylation. Hemoglobin 1997; 21(2):179-186.
-
(1997)
Hemoglobin
, vol.21
, Issue.2
, pp. 179-186
-
-
Ohba, Y.1
Hattori, Y.2
Sakata, S.3
Yamashiro, Y.4
Okayama, N.5
Hirano, T.6
Nakanishi, T.7
Miyazaki, A.8
Shimizu, A.9
-
7
-
-
7144264399
-
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
-
8
-
-
0021749376
-
2 N methionyl-2 (NA2) His→Pro]: A new β chain variant having an extended N-terminus
-
2 N methionyl-2 (NA2) His→Pro]: a new β chain variant having an extended N-terminus. FEBS Lett 1984; 178(2):315-318.
-
(1984)
FEBS Lett
, vol.178
, Issue.2
, pp. 315-318
-
-
Blouquit, Y.1
Arous, N.2
Lena, D.3
Delanoe-Garin, J.4
Lacombe, C.5
Bardakdjian, J.6
Vovan, L.7
Orsini, A.8
Rosa, J.9
Galacteros, F.10
-
9
-
-
0012347434
-
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
-
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
-
-
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
-
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
-
-
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.
-
-
-
-
14
-
-
0021399557
-
Molecular characterization of seven β-thalassemia mutations in Asian Indians
-
Kazazian HH Jr, Orkin SH, Antonarakis SE, Sexton JP, Boehm CD, Goff SC, Waber PG. Molecular characterization of seven β-thalassemia mutations in Asian Indians. EMBO J 1984; 3(3):593-596.
-
(1984)
EMBO J
, vol.3
, Issue.3
, pp. 593-596
-
-
Kazazian Jr, H.H.1
Orkin, S.H.2
Antonarakis, S.E.3
Sexton, J.P.4
Boehm, C.D.5
Goff, S.C.6
Waber, P.G.7
-
15
-
-
0026610808
-
0-thalassaemia mutation (codon 15, TGG→TGA) is prevalent in a population of central Portugal
-
0-thalassaemia mutation (codon 15, TGG→TGA) is prevalent in a population of central Portugal. Br J Haematol 1992; 80(4):567-568.
-
(1992)
Br J Haematol
, vol.80
, Issue.4
, pp. 567-568
-
-
Ribeiro, M.L.S.1
Baysal, E.2
Kutlar, F.3
Tamagnini, G.P.4
Goncalves, P.5
Lopes, D.6
Huisman, T.H.J.7
-
16
-
-
0033987736
-
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
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