-
1
-
-
0014292066
-
Evidence for multiple structural genes for the γ chain of human fetal hemoglobin
-
Schroeder WA, Huisman THJ, Shelton JR, Shelton JB, Kleihauer EF, Dozy AM, Robberson B: Evidence for multiple structural genes for the γ chain of human fetal hemoglobin. Proc Natl Acad Sci USA 60:537, 1968.
-
(1968)
Proc Natl Acad Sci USA
, vol.60
, pp. 537
-
-
Schroeder, W.A.1
Huisman, T.H.J.2
Shelton, J.R.3
Shelton, J.B.4
Kleihauer, E.F.5
Dozy, A.M.6
Robberson, B.7
-
2
-
-
0018952782
-
Aγ-globin genes: Complete nucleotide sequences suggest that DNA can be exchanged between these duplicated genes
-
Aγ-globin genes: Complete nucleotide sequences suggest that DNA can be exchanged between these duplicated genes. Cell 21:627, 1980.
-
(1980)
Cell
, vol.21
, pp. 627
-
-
Slightom, J.L.1
Blechl, A.E.2
Smithies, O.3
-
3
-
-
0019790943
-
A history of the human fetal globin gene duplication
-
Shen SH, Slightom JL, Smithies O: A history of the human fetal globin gene duplication. Cell 26:191, 1981.
-
(1981)
Cell
, vol.26
, pp. 191
-
-
Shen, S.H.1
Slightom, J.L.2
Smithies, O.3
-
7
-
-
0001441465
-
Conventional isoelectric focusing and immobilized pH gradients for hemoglobin separation and identification
-
Huisman THJ (ed): Edinburgh: Churchill Livingstone
-
Righetti PG, Gianazza E, Bianchi-Bosisio A, Cossu G: Conventional isoelectric focusing and immobilized pH gradients for hemoglobin separation and identification. In Huisman THJ (ed): "The Haemoglobinopathies." Vol. 15. Edinburgh: Churchill Livingstone, 1986, p. 47.
-
(1986)
The Haemoglobinopathies
, vol.15
, pp. 47
-
-
Righetti, P.G.1
Gianazza, E.2
Bianchi-Bosisio, A.3
Cossu, G.4
-
9
-
-
0022514967
-
The gamma globin chain heterogeneity of the Sardinian newborn baby
-
Manca L, Formato M, Demoro P, Pilo G, Gallisai D, Orzalesi M, Masala B: The gamma globin chain heterogeneity of the Sardinian newborn baby. Hemoglobin 10:519, 1986.
-
(1986)
Hemoglobin
, vol.10
, pp. 519
-
-
Manca, L.1
Formato, M.2
Demoro, P.3
Pilo, G.4
Gallisai, D.5
Orzalesi, M.6
Masala, B.7
-
11
-
-
0022460617
-
Separation of normal and abnormal hemoglobin chains by reversed-phase high-performance liquid chromatography
-
Kutlar F, Kutlar A, Huisman THJ: Separation of normal and abnormal hemoglobin chains by reversed-phase high-performance liquid chromatography. J Chromatogr 357:147, 1986.
-
(1986)
J Chromatogr
, vol.357
, pp. 147
-
-
Kutlar, F.1
Kutlar, A.2
Huisman, T.H.J.3
-
12
-
-
1842273101
-
Structural studies of aminoethylated hemoglobins by automatic peptide chromatography
-
Jones RT: Structural studies of aminoethylated hemoglobins by automatic peptide chromatography. Cold Spring Harbor Symp Quant Biol 29:297, 1964.
-
(1964)
Cold Spring Harbor Symp Quant Biol
, vol.29
, pp. 297
-
-
Jones, R.T.1
-
13
-
-
0008280645
-
HPLC of globin chains and of peptides in the identification of hemoglobin variants
-
Huisman THJ (ed): Edinburgh: Churchill Livingstone
-
Schroeder WA: HPLC of globin chains and of peptides in the identification of hemoglobin variants. In Huisman THJ (ed): "The Hemoglobinopathies," Vol. 15. Edinburgh: Churchill Livingstone, 1986, p. 143.
-
(1986)
The Hemoglobinopathies
, vol.15
, pp. 143
-
-
Schroeder, W.A.1
-
14
-
-
0018568310
-
Separation of tryptic peptides of normal and abnormal α, β, γ, and δ hemoglobin chains by high performance liquid chromatography
-
Wilson JB, Lam H, Pravatmuang P, Huisman THJ: Separation of tryptic peptides of normal and abnormal α, β, γ, and δ hemoglobin chains by high performance liquid chromatography. J Chromatogr 179:271, 1979.
-
(1979)
J Chromatogr
, vol.179
, pp. 271
-
-
Wilson, J.B.1
Lam, H.2
Pravatmuang, P.3
Huisman, T.H.J.4
-
15
-
-
0025992788
-
γ Chain abnormalities and δ-globin gene rearrangements in newborn babies of various populations
-
Huisman THJ, Kutlar F, Gu L-H: γ Chain abnormalities and δ-globin gene rearrangements in newborn babies of various populations. Hemoglobin 15:349, 1991.
-
(1991)
Hemoglobin
, vol.15
, pp. 349
-
-
Huisman, T.H.J.1
Kutlar, F.2
Gu, L.-H.3
-
16
-
-
0021996070
-
Fetal hemoglobin variants identified in adults through restriction endonuclease gene mapping methodology
-
Nakatsuji T, Burnley MS, Huisman THJ: Fetal hemoglobin variants identified in adults through restriction endonuclease gene mapping methodology. Blood 66:803, 1985.
-
(1985)
Blood
, vol.66
, pp. 803
-
-
Nakatsuji, T.1
Burnley, M.S.2
Huisman, T.H.J.3
-
17
-
-
0026497827
-
Heterozygosity for the IVS-I-5 (G→C) mutation with a G→a change at codon 18 (Val→Met; Hb Baden) in cis and a T→a mutation at codon 126 (Val→Gly; Hb Dhonburi) in trans resulting in a thalassemia intermedia
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Divoky V, Bissé E, Wilson JB, Gu L-H, Wieland H, Heinrichs I, Prior JF, Huisman THJ: Heterozygosity for the IVS-I-5 (G→C) mutation with a G→A change at codon 18 (Val→Met; Hb Baden) in cis and a T→A mutation at codon 126 (Val→Gly; Hb Dhonburi) in trans resulting in a thalassemia intermedia. Biochim Biophys Acta 1180:173, 1992.
-
(1992)
Biochim Biophys Acta
, vol.1180
, pp. 173
-
-
Divoky, V.1
Bissé, E.2
Wilson, J.B.3
Gu, L.-H.4
Wieland, H.5
Heinrichs, I.6
Prior, J.F.7
Huisman, T.H.J.8
-
18
-
-
0024211736
-
High-performance liquid chromatographic separation of human haemoglobins. Simultaneous quantitation of foetal and glycated haemoglobins
-
Bissé E, Wieland H: High-performance liquid chromatographic separation of human haemoglobins. Simultaneous quantitation of foetal and glycated haemoglobins. J Chromatogr 434:95, 1988.
-
(1988)
J Chromatogr
, vol.434
, pp. 95
-
-
Bissé, E.1
Wieland, H.2
-
21
-
-
0024544523
-
Mutant fetal hemoglobin causing cyanosis in a newborn
-
Priest JR, Watterson J, Jones RT, Faassen AE, Hedlund BE: Mutant fetal hemoglobin causing cyanosis in a newborn. Pediatrics 83:734, 1989.
-
(1989)
Pediatrics
, vol.83
, pp. 734
-
-
Priest, J.R.1
Watterson, J.2
Jones, R.T.3
Faassen, A.E.4
Hedlund, B.E.5
-
22
-
-
0026731533
-
292(F8)His→Tyr
-
292(F8)His→Tyr. Hemoglobin 16:389, 1992.
-
(1992)
Hemoglobin
, vol.16
, pp. 389
-
-
Molchanova, T.P.1
Wilson, J.B.2
Gu, L.-H.3
Hain, R.D.W.4
Chang, L.S.5
Poon, A.O.6
Huisman, T.H.J.7
-
24
-
-
0017213963
-
Another form of hereditary persistence of fetal hemoglobin (the Atlanta type)?
-
Altay C, Huisman THJ, Schroeder WA: Another form of hereditary persistence of fetal hemoglobin (the Atlanta type)? Hemoglobin 1:125, 1977.
-
(1977)
Hemoglobin
, vol.1
, pp. 125
-
-
Altay, C.1
Huisman, T.H.J.2
Schroeder, W.A.3
-
26
-
-
0028177922
-
The -158 (C→T) promoter mutation is responsible for the increased transcription of the 3′ γ gene in the Atlanta type of hereditary persistence of fetal hemoglobin
-
Efremov DG, Dimovski AJ, Huisman THJ: The -158 (C→T) promoter mutation is responsible for the increased transcription of the 3′ γ gene in the Atlanta type of hereditary persistence of fetal hemoglobin. Blood 83:3350, 1994.
-
(1994)
Blood
, vol.83
, pp. 3350
-
-
Efremov, D.G.1
Dimovski, A.J.2
Huisman, T.H.J.3
-
29
-
-
0027989558
-
Gγ variant with a threonine residue at position γ75, characterized by mass spectrometric techniques
-
Gγ variant with a threonine residue at position γ75, characterized by mass spectrometric techniques. Hemoglobin 18:307, 1994.
-
(1994)
Hemoglobin
, vol.18
, pp. 307
-
-
Ferranti, P.1
Barone, F.2
Pucci, P.3
Malorni, A.4
Marino, G.5
Pilo, G.6
Manca, L.7
Masala, B.8
-
32
-
-
0022338890
-
T in different populations and its use in evaluating γ gene expression in association with thalassemia
-
T in different populations and its use in evaluating γ gene expression in association with thalassemia. Hum Genet 71:127, 1985.
-
(1985)
Hum Genet
, vol.71
, pp. 127
-
-
Huisman, T.H.J.1
Kutlar, F.2
Nakatsuji, T.3
Bruce-Tagoe, A.4
Kilinç, Y.5
Cauchi, M.N.6
Romero Garcia, C.7
-
33
-
-
0023607258
-
T25(B7)Gly→Arg: A new slow-moving unstable fetal hemoglobin variant
-
T25(B7)Gly→Arg: A new slow-moving unstable fetal hemoglobin variant. Hemoglobin 11:464, 1987.
-
(1987)
Hemoglobin
, vol.11
, pp. 464
-
-
Hu, H.1
Ma, M.2
-
34
-
-
0022371132
-
Aγ variant with two amino acid substitutions, 75(E19)Ile→Thr and 73(E17)Asp→Asn, which can be identified in adults by gene-mapping analysis
-
Aγ variant with two amino acid substitutions, 75(E19)Ile→Thr and 73(E17)Asp→Asn, which can be identified in adults by gene-mapping analysis. Biochim Biophys Acta 832:242, 1985.
-
(1985)
Biochim Biophys Acta
, vol.832
, pp. 242
-
-
Chen, S.-S.1
Webber, B.B.2
Wilson, J.B.3
Huisman, T.H.J.4
-
35
-
-
0019513348
-
Survey of cord blood hemoglobin and identification of two new γ chain variants
-
Fuyuno K, Torigoe T, Ohba Y, Matsuoka M, Miyaji T: Survey of cord blood hemoglobin and identification of two new γ chain variants. Hemoglobin 5:139, 1981.
-
(1981)
Hemoglobin
, vol.5
, pp. 139
-
-
Fuyuno, K.1
Torigoe, T.2
Ohba, Y.3
Matsuoka, M.4
Miyaji, T.5
-
36
-
-
0020625717
-
Alpha chain and gamma chain abnormal hemoglobins in newborn babies: Structural and genetic aspects
-
Nakatsuji T, Carver J, Wilson JB, Lam H, Reese AL, Nagle S, Miwa S, Huisman THJ: Alpha chain and gamma chain abnormal hemoglobins in newborn babies: Structural and genetic aspects. Am J Hematol 14:121, 1983.
-
(1983)
Am J Hematol
, vol.14
, pp. 121
-
-
Nakatsuji, T.1
Carver, J.2
Wilson, J.B.3
Lam, H.4
Reese, A.L.5
Nagle, S.6
Miwa, S.7
Huisman, T.H.J.8
-
39
-
-
0020615882
-
2 121 (GH4) Glu→Lys). A new fetal hemoglobin variant
-
2 121 (GH4) Glu→Lys). A new fetal hemoglobin variant. Hemoglobin 7:79, 1983.
-
(1983)
Hemoglobin
, vol.7
, pp. 79
-
-
Carè, A.1
Marinucci, M.2
Massa, A.3
Maffi, D.4
Sposi, N.M.5
Improta, T.6
Tentori, L.7
-
40
-
-
0021101062
-
Gamma thalassemia resulting from the deletion of a γ-globin gene
-
Sukumaran PK, Nakatsuji T, Gardiner MB, Reese AL, Gilman JG, Huisman THJ: Gamma thalassemia resulting from the deletion of a γ-globin gene. Nucleic Acids Res 11:4643, 1983.
-
(1983)
Nucleic Acids Res
, vol.11
, pp. 4643
-
-
Sukumaran, P.K.1
Nakatsuji, T.2
Gardiner, M.B.3
Reese, A.L.4
Gilman, J.G.5
Huisman, T.H.J.6
-
41
-
-
0020611705
-
T variant of fetal hemoglobin in newborn babies from several countries
-
T variant of fetal hemoglobin in newborn babies from several countries. Am J Hematol 14:133, 1983.
-
(1983)
Am J Hematol
, vol.14
, pp. 133
-
-
Huisman, T.H.J.1
Reese, A.L.2
Gardiner, M.B.3
Wilson, J.B.4
Lam, H.5
Reynolds, A.6
Nagle, S.7
Trowell, P.8
Zeng, Y.T.9
Huang, S.Z.10
Sukumaran, P.K.11
Miwa, S.12
Efremov, G.D.13
Petkov, G.14
Sciarratta, G.V.15
Sansone, G.16
-
42
-
-
0027166866
-
The structure and function of normal and abnormal haemoglobins
-
Weatherall DJ, Higgs DR (eds): London: Saunders
-
Huisman THJ: The structure and function of normal and abnormal haemoglobins. In Weatherall DJ, Higgs DR (eds): "The Hemoglobinopathies," Bailliere's Clinical Haematology, Vol. 6. London: Saunders, 1993, p. 1.
-
(1993)
"The Hemoglobinopathies," Bailliere's Clinical Haematology
, vol.6
, pp. 1
-
-
Huisman, T.H.J.1
-
43
-
-
0025925290
-
2: Origin, evolution, and aftermath
-
2: Origin, evolution, and aftermath. Blood, 78:2165, 1991.
-
(1991)
Blood
, vol.78
, pp. 2165
-
-
Steinberg, M.H.1
Adams III, J.G.2
-
45
-
-
0023487372
-
Gγ non-anemic person
-
Stamatoyannopoulos G, Neinhuis AW (eds): New York: Alan R. Liss
-
Gγ non-anemic person. In Stamatoyannopoulos G, Neinhuis AW (eds): "Progress in Clinical and Biological Research," Developmental Control of Globin Gene Expression, Vol. 251. New York: Alan R. Liss, 1987, p. 415.
-
(1987)
"Progress in Clinical and Biological Research," Developmental Control of Globin Gene Expression
, vol.251
, pp. 415
-
-
Gilman, J.G.1
Kutlar, F.2
Johnson, M.E.3
Huisman, T.H.J.4
-
46
-
-
0029910109
-
Variability in the fetal hemoglobin level of the normal adult
-
Leonova JYe, Kazanetz EG, Smetanina NS, Adekile AD, Efremov GD, Huisman THJ: Variability in the fetal hemoglobin level of the normal adult. Am J Hematol 53:59, 1996.
-
(1996)
Am J Hematol
, vol.53
, pp. 59
-
-
Leonova, J.Ye.1
Kazanetz, E.G.2
Smetanina, N.S.3
Adekile, A.D.4
Efremov, G.D.5
Huisman, T.H.J.6
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