| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| 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 |
| 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. |
an abnormal hemoglobin, hb owari [alpha 121 (h 4) val----met], was discovered in seven japanese. |
1986-05-13 |
2023-08-11 |
Not clear |
| D Loukopoulos, C Poyart, J Delanoe-Garin, C Matsis, N Arous, J Kister, A Loutradi-Anagnostou, Y Blouquit, P Fessas, J Thille. Hemoglobin San Diego/beta zero thalassemia in a Greek adult. Hemoglobin. vol 10. issue 2. 1986-05-13. PMID:3957694. |
interaction of beta zero thalassemia with hb san diego [a high affinity hemoglobin variant, alpha 2 beta (2)109(g11)val----met] in a 29-year-old greek male is described. |
1986-05-13 |
2023-08-11 |
Not clear |
| E E Mayne, G E Elder, T R Lappin, L A Ferguso. Hb M Iwate [alpha (2)87His----Tyr beta 2]: de novo mutation in an Irish family. Hemoglobin. vol 10. issue 2. 1986-05-13. PMID:3957697. |
hb m iwate [alpha (2)87his----tyr beta 2]: de novo mutation in an irish family. |
1986-05-13 |
2023-08-11 |
Not clear |
| T Maita, Y Tanioka, S Nakayama, G Matsud. Amino-acid sequences of the two major components of adult hemoglobins from the stump-tail monkey, Macaca speciosa. Biological chemistry Hoppe-Seyler. vol 366. issue 12. 1986-04-22. PMID:4091973. |
only one amino-acid difference was found between the alpha chains from hb 1 and hb 2 at the 15th position from the n-terminus. |
1986-04-22 |
2023-08-11 |
human |
| F Xiong, K G Yang, C C Liang, Y W Huang, R X Wang, N J Zhan. [Hb J Camagüey [alpha 141 (HC3) Arg-Gly]--the first case identified in China]. Zhongguo yi xue ke xue yuan xue bao. Acta Academiae Medicinae Sinicae. vol 7. issue 2. 1986-04-09. PMID:2936500. |
[hb j camagüey [alpha 141 (hc3) arg-gly]--the first case identified in china]. |
1986-04-09 |
2023-08-11 |
Not clear |