| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| W Nakamoto, P E Machad. Characterization of the hemoglobins and globins of Synbranchus marmoratus Bloch, 1795 (Pisces, Synbranchidae). Comparative biochemistry and physiology. B, Comparative biochemistry. vol 84. issue 3. 1986-10-10. PMID:3743031. |
it is suggested that the probable tetrameric constitution of the hemoglobin of synbranchus marmoratus bloch, 1795 is hb i (alpha (2)2 gamma 2), hb ii (alpha (1)2 gamma 2) and hb iii (alpha (1)2 beta 2). |
1986-10-10 |
2023-08-11 |
Not clear |
| K D Lanclos, A Kutlar, F Kutlar, P J Ojwang, A L Reese, T H Huisma. The effect of alpha-thalassemia on the level of hybrid hemoglobin variants in heterozygotes. Hemoglobin. vol 10. issue 4. 1986-10-01. PMID:2427479. |
hb kenya, composed of normal alpha and gamma-beta hybrid chains, is heat labile, has a decreased ability to combine with alpha chains, and its level in heterozygotes is greatly decreased when a concomitant alpha-chain deficiency (alpha-thalassemia) is present. |
1986-10-01 |
2023-08-11 |
Not clear |
| K D Lanclos, A Kutlar, F Kutlar, P J Ojwang, A L Reese, T H Huisma. The effect of alpha-thalassemia on the level of hybrid hemoglobin variants in heterozygotes. Hemoglobin. vol 10. issue 4. 1986-10-01. PMID:2427479. |
such a posttranslational control mechanism was not observed for hb lepore, with normal alpha chains and delta-beta hybrid chains, and hb p-nilotic, with normal alpha chains and beta-delta hybrid chains. |
1986-10-01 |
2023-08-11 |
Not clear |
| K D Lanclos, A Kutlar, F Kutlar, P J Ojwang, A L Reese, T H Huisma. The effect of alpha-thalassemia on the level of hybrid hemoglobin variants in heterozygotes. Hemoglobin. vol 10. issue 4. 1986-10-01. PMID:2427479. |
hb p-nilotic is more heat stable than hb a and its in vitro formation is increased over that of hb s, and perhaps even hb a, in conditions of severe alpha chain deficiency. |
1986-10-01 |
2023-08-11 |
Not clear |
| A E Felice, M P Cleek, E M Marino, K M McKie, V C McKie, B K Chang, T H Huisma. Different zeta globin gene deletions among black Americans. Human genetics. vol 73. issue 3. 1986-09-17. PMID:3015767. |
hematologic data on carriers of the zeta globin gene deletions in association with hb as, ss, and sc suggest that these deletions have no effect on the function of the adult alpha globin genes. |
1986-09-17 |
2023-08-11 |
human |
| A J Lambridis, M Ramsay, T Jenkin. The haematological puzzle of Hb J Cape Town is partly solved. British journal of haematology. vol 63. issue 2. 1986-08-19. PMID:3718876. |
molecular studies have shown that the mutation giving rise to hb j cape town (alpha 92 arg----gln) is situated on a chromosome from which the other alpha-globin gene has been deleted. |
1986-08-19 |
2023-08-11 |
Not clear |
| J M White, M Byrne, R Richards, T Buchanan, E Katsoulis, K Weerasing. Red cell genetic abnormalities in Peninsular Arabs: sickle haemoglobin, G6PD deficiency, and alpha and beta thalassaemia. Journal of medical genetics. vol 23. issue 3. 1986-07-25. PMID:3723553. |
the frequencies of four major red cell genetic defects, sickle haemoglobin (hb s), glucose 6 phosphate dehydrogenase deficiency (g6pd), and alpha and beta thalassaemia, have been determined in nearly 5000 subjects from the three major peninsular arab states, namely yemen (north and south), the united arab emirates, and oman. |
1986-07-25 |
2023-08-11 |
human |
| J M White, M Byrne, R Richards, T Buchanan, E Katsoulis, K Weerasing. Red cell genetic abnormalities in Peninsular Arabs: sickle haemoglobin, G6PD deficiency, and alpha and beta thalassaemia. Journal of medical genetics. vol 23. issue 3. 1986-07-25. PMID:3723553. |
all four defects are common with an overall pattern of alpha thalassaemia greater than g6pd deficiency greater than beta thalassaemia greater than hb a/s. |
1986-07-25 |
2023-08-11 |
human |
| H Simpkins, A V Hill, S Derry, J B Clegg, D J Weatheral. Interaction of five globin gene abnormalities in a Cambodian family. British journal of haematology. vol 63. issue 1. 1986-07-10. PMID:3754762. |
one child has hb e and typical hb h disease, while his mother has the form of hb h disease associated with hb constant spring interacting with hb e. quantitation of hbs e and a2 by globin chain separation and triton/urea gel electrophoresis support the concept that hb h/constant spring disease is a more severe form of alpha thalassaemia than hb h disease. |
1986-07-10 |
2023-08-11 |
Not clear |
| T H Huisman, J B Wilson, A Kutlar, K G Yang, S S Chen, B B Webber, C Altay, A V Martine. Hb J-Antakya or alpha 2 beta (2)65(E9)Lys----Met in a Turkish family and Hb complutense or alpha 2 beta (2)127(H5)Gln----Glu in a Spanish family; correction of a previously published identification. Biochimica et biophysica acta. vol 871. issue 2. 1986-07-09. PMID:3707969. |
hb j-antakya or alpha 2 beta (2)65(e9)lys----met in a turkish family and hb complutense or alpha 2 beta (2)127(h5)gln----glu in a spanish family; correction of a previously published identification. |
1986-07-09 |
2023-08-11 |
Not clear |
| T H Huisman, J B Wilson, A Kutlar, K G Yang, S S Chen, B B Webber, C Altay, A V Martine. Hb J-Antakya or alpha 2 beta (2)65(E9)Lys----Met in a Turkish family and Hb complutense or alpha 2 beta (2)127(H5)Gln----Glu in a Spanish family; correction of a previously published identification. Biochimica et biophysica acta. vol 871. issue 2. 1986-07-09. PMID:3707969. |
almost 10 years ago we reported in this journal the characterization of hb hacettepe or alpha 2 beta (2)127(h5)gln----glu. |
1986-07-09 |
2023-08-11 |
Not clear |
| T H Huisman, J B Wilson, A Kutlar, K G Yang, S S Chen, B B Webber, C Altay, A V Martine. Hb J-Antakya or alpha 2 beta (2)65(E9)Lys----Met in a Turkish family and Hb complutense or alpha 2 beta (2)127(H5)Gln----Glu in a Spanish family; correction of a previously published identification. Biochimica et biophysica acta. vol 871. issue 2. 1986-07-09. PMID:3707969. |
the variant (alpha 2 beta (2)65(e9)lys----met) was (re)named hb j-antakya, after the city where the family resides. |
1986-07-09 |
2023-08-11 |
Not clear |
| C T Craescu, C Schaeffer, J Mispelter, J Garin, J Ros. High resolution NMR studies of histidine-substituted and histidine-perturbed hemoglobin variants. Histidine assignments, electrostatic interactions at the protein surface, and implications for hemoglobin S polymerization. The Journal of biological chemistry. vol 261. issue 17. 1986-07-09. PMID:3711114. |
studies with hb variants in which a histidine is perturbed by a neighboring substitution suggest additional assignments for his alpha 50 and his alpha 89 and demonstrate a strong dependence of the imidazole ring pk on hydrogen bond interactions and on the net charge of neighboring residues. |
1986-07-09 |
2023-08-11 |
human |
| A V Hill, D K Bowden, D J Weatherall, J B Cleg. Chromosomes with one, two, three, and four fetal globin genes: molecular and hematologic analysis. Blood. vol 67. issue 6. 1986-07-03. PMID:2423158. |
homozygotes for triple- and single-gamma genes have normal hematologic findings, normal hemoglobin f (hbf) levels, and when there is coexisting alpha thalassemia, appropriate levels of bart's hb (gamma 4) at birth. |
1986-07-03 |
2023-08-11 |
Not clear |
| Y Blouquit, M D Rhoda, J Delanoe-Garin, R Rosa, J C Prome, C Poyart, G Puzo, J M Bernassau, J Ros. Glycerated hemoglobin, alpha 2A beta 2(82) (EF6) N epsilon-glyceryllysine. A new post-translational modification occurring in erythrocyte bisphosphoglyceromutase deficiency. The Journal of biological chemistry. vol 261. issue 15. 1986-06-19. PMID:3009476. |
it was concluded that hbx was a glycerylated hb, alpha 2a beta 2(82) (ef6) n epsilon-glyceryllysine, to our knowledge the first example of glycerylated protein. |
1986-06-19 |
2023-08-11 |
human |
| S J Edelstein, C Poyart, Y Blouquit, J Kiste. Self-association of haemoglobin Olympia (alpha 2 beta 2 20 (B2) Val----Met). A human haemoglobin bearing a substitution at the surface of the molecule. Journal of molecular biology. vol 187. issue 2. 1986-06-13. PMID:3701868. |
oxygenation measurements at equilibrium were carried out for solutions of pure haemoglobin (hb) olympia (alpha 2 beta 2 20 (b2) val----met) at 200 microm (haem) and revealed a high oxygen affinity (p50 = 4.2 torr at ph 7.20, 25 degrees c) compared to hba (p50 = 5.6 torr), with the hill coefficient (eta h) reduced from the normal value of 2.9 to 2.5 for hb olympia at neutral ph. |
1986-06-13 |
2023-08-11 |
human |
| M D Rhoda, N Arous, M C Garel, M Mazarin, N Monplaisir, F Braconnier, J Rosa, M Cohen-Solal, F Galactero. Interaction of hemoglobin Siriraj with hemoglobin S: a mild sickle cell syndrome. Hemoglobin. vol 10. issue 1. 1986-05-22. PMID:3754242. |
some properties of hb siriraj are compared, particularly, with hb c [alpha 2 beta 26(a3)glu----lys], and a study of its in vitro interaction with hb s is discussed. |
1986-05-22 |
2023-08-11 |
Not clear |
| L Hsu, Q F Lung, Z N Tang, Y J Fei, C W Su, S S Chen, B B Webber, J B Wilson, F Kutlar, T H Huisma. Hb Chapel Hill or alpha 274(EF3)Asp----Gly beta 2 observed in a Chinese family in association with beta-thalassemia. Hemoglobin. vol 10. issue 1. 1986-05-22. PMID:3754243. |
hb chapel hill or alpha 274(ef3)asp----gly beta 2 observed in a chinese family in association with beta-thalassemia. |
1986-05-22 |
2023-08-11 |
Not clear |
| K Hidaka, I Iuchi, S Shimasaki, W Mizuta, M Takatsuka, T Mori, A Tohdoh, M Matsu. The survey of abnormal hemoglobins in the Kobe district: Hb G-Coushatta [beta 22(B4)Glu----Ala], Hb Ankara (beta 10(A7)Ala----Asp], Hb Handa [alpha 90(FG2)Lys----Met], and Hb J-Habana [alpha 71(E20)Ala----Glu]. Hemoglobin. vol 10. issue 1. 1986-05-22. PMID:3957691. |
the survey of abnormal hemoglobins in the kobe district: hb g-coushatta [beta 22(b4)glu----ala], hb ankara (beta 10(a7)ala----asp], hb handa [alpha 90(fg2)lys----met], and hb j-habana [alpha 71(e20)ala----glu]. |
1986-05-22 |
2023-08-11 |
Not clear |
| T Harano, K Harano, S Ued. Hb Owari [alpha 121 (H 4) Val----Met]: a new hemoglobin variant with a neutral-to-neutral amino acid substitution detected by isoelectric focusing. Hemoglobin. vol 10. issue 2. 1986-05-13. PMID:3754245. |
hb owari [alpha 121 (h 4) val----met]: a new hemoglobin variant with a neutral-to-neutral amino acid substitution detected by isoelectric focusing. |
1986-05-13 |
2023-08-11 |
Not clear |