| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| F Kutlar, Y J Fei, J B Wilson, A Kutlar, T H Huisma. Detection of the embryonic zeta chain in blood from newborn babies by reversed-phase high-performance liquid chromatography. Journal of chromatography. vol 394. issue 2. 1987-09-28. PMID:2442182. |
the quantity of zeta in normal babies is less than 0.7% [% of (alpha + zeta)] and is dependent upon the maturity of the baby as it was only present in babies with low levels of beta chain or hemoglobin (hb) a. |
1987-09-28 |
2023-08-11 |
Not clear |
| A E Felice, K M McKie, M P Cleek, E M Marino, A Kutlar, V C McKi. Effects of alpha-thalassemia-2 on the developmental changes of hematological values in children with sickle cell disease from Georgia. American journal of hematology. vol 25. issue 4. 1987-09-18. PMID:2441597. |
the hematology and pathophysiology of sickle cell disease during the postnatal development of younger hemoglobin (hb) s homozygotes (ss) could be considerably affected by a variability of alpha globin gene numbers. |
1987-09-18 |
2023-08-11 |
Not clear |
| A E Felice, K M McKie, M P Cleek, E M Marino, A Kutlar, V C McKi. Effects of alpha-thalassemia-2 on the developmental changes of hematological values in children with sickle cell disease from Georgia. American journal of hematology. vol 25. issue 4. 1987-09-18. PMID:2441597. |
around the age of 7, the ss patients with -alpha/-alpha developed a higher hb concentration than that of the ss (-alpha/alpha alpha), which in turn was higher than that of the ss (alpha alpha/alpha alpha). |
1987-09-18 |
2023-08-11 |
Not clear |
| A E Felice, K M McKie, M P Cleek, E M Marino, A Kutlar, V C McKi. Effects of alpha-thalassemia-2 on the developmental changes of hematological values in children with sickle cell disease from Georgia. American journal of hematology. vol 25. issue 4. 1987-09-18. PMID:2441597. |
the emergence of this difference coincided with a developmental increase of the mean corpuscular hemoglobin concentration (mchc) in patients with ss (alpha alpha/alpha alpha) and the decline of hb f % under 15%. |
1987-09-18 |
2023-08-11 |
Not clear |
| A E Felice, K M McKie, M P Cleek, E M Marino, A Kutlar, V C McKi. Effects of alpha-thalassemia-2 on the developmental changes of hematological values in children with sickle cell disease from Georgia. American journal of hematology. vol 25. issue 4. 1987-09-18. PMID:2441597. |
although the proportion of hb f was independent of alpha globin gene numbers, the absence of hb bart's suggested that alpha-thalassemia promotes the intracellular assembly of hb f over hb s tetramers. |
1987-09-18 |
2023-08-11 |
Not clear |
| K Adachi, J Kim, T R Kinney, T Asakur. Effect of the beta 73 amino acid on the hydrophobicity, solubility, and the kinetics of polymerization of deoxyhemoglobin S. The Journal of biological chemistry. vol 262. issue 22. 1987-09-17. PMID:3611079. |
effect of the beta 73 amino acid on the hydrophobicity, solubility, and the kinetics of polymerization of deoxyhemoglobin s. the role of asp-beta 73 on the surface hydrophobicity and solubility of hemoglobin was studied using hb a, hb s, hb c harlem (alpha 2 beta 2val-6,asn-73), and hb korle bu (alpha 2 beta 2asn-73). |
1987-09-17 |
2023-08-11 |
Not clear |
| C Ho, I M Russ. Proton NMR studies of the molecular basis for the anti-sickling activity of non-covalent antisickling compounds. Progress in clinical and biological research. vol 240. 1987-09-08. PMID:3615505. |
with the exception of l-valine, all of these molecules are known to inhibit the polymerization of deoxy hb s. we have found that for the compounds with antisickling activity, there are at least two binding sites to the hb s molecule, one at or near the heme pockets of the alpha and beta chains and the other one in the vicinity of the beta 6 mutation site. |
1987-09-08 |
2023-08-11 |
Not clear |
| D K Bowden, A V Hill, D J Weatherall, J B Cleg. High frequency of beta thalassaemia in a small island population in Melanesia. Journal of medical genetics. vol 24. issue 6. 1987-08-28. PMID:2441058. |
coexistent alpha + thalassaemia leads to better haemoglobinised and larger red cells than are seen in simple beta thalassaemia heterozygotes and screening for the latter can only be reliably carried out by hb a2 estimation. |
1987-08-28 |
2023-08-11 |
Not clear |
| J M Gonzalez Redondo, A Sicilia, M J Murga, A Kutlar, J B Wilson, T H Huisma. Hb E-Saskatoon or alpha 2 beta 2(22)(B4)Glu----Lys in a Spanish family. Hemoglobin. vol 11. issue 1. 1987-07-17. PMID:3108201. |
hb e-saskatoon or alpha 2 beta 2(22)(b4)glu----lys in a spanish family. |
1987-07-17 |
2023-08-11 |
Not clear |
| C Lacombe, J Soria, N Arous, Y Blouquit, J Bardakdjian, J Riou, F Galactero. A new case of Hb Dagestan [alpha 60(E9)Lys----Glu]. Hemoglobin. vol 11. issue 1. 1987-07-17. PMID:3108202. |
a new case of hb dagestan [alpha 60(e9)lys----glu]. |
1987-07-17 |
2023-08-11 |
Not clear |
| J Bardakdjian, N Arous, J Kister, Y Blouquit, T Giacomini, C Lacombe, J Riou, R Hafsia, J Rosa, F Galactero. Further characterization of Hb Henri Mondor or alpha 2 beta 2(26)(B8)Glu----Val. Hemoglobin. vol 11. issue 1. 1987-07-17. PMID:3583762. |
further characterization of hb henri mondor or alpha 2 beta 2(26)(b8)glu----val. |
1987-07-17 |
2023-08-11 |
human |
| J M Gonzalez Redondo, J B Wilson, A Kutlar, T H Huisman, A Sicilia, C Romero, I Fernandes Fuerte. Hb J-Pontoise or alpha 2(63)(E12)Ala----Asp beta 2 in four members of a Spanish family. Hemoglobin. vol 11. issue 1. 1987-07-17. PMID:3583765. |
hb j-pontoise or alpha 2(63)(e12)ala----asp beta 2 in four members of a spanish family. |
1987-07-17 |
2023-08-11 |
Not clear |
| Y Blouquit, M D Rhoda, J Delanoe-Garin, R Rosa, J C Prome, C Poyart, G Puzo, J M Bernassaus, J Ros. Glycerated hemoglobin alpha 2 beta 2(82) (EF6) N-epsilon-glyceryllysine: a new post-translational modification occurring in erythrocyte bisphosphoglyceromutase deficiency. Biomedica biochimica acta. vol 46. issue 2-3. 1987-06-26. PMID:3036109. |
it was concluded that hbx was a glycerylated hb: alpha 2 a beta 2(82) (ef6) n-epsilon-glyceryllysine, to our knowledge the first example of glycerylated protein. |
1987-06-26 |
2023-08-11 |
human |
| A Bennu. A coupling mechanism to inter-relate regulatory with haem-haem interactions of haemoglobin. Biomedica biochimica acta. vol 46. issue 2-3. 1987-06-26. PMID:3593312. |
the me2+ (zn2+ or mg2+)-dependent increase in the oxygenation of haemoglobin (hb) is examined theoretically using an overview in scale of the interface of the alpha 1 beta 2 dimer of hb. |
1987-06-26 |
2023-08-11 |
Not clear |
| B F Wiedermann, K Indrak, J B Wilson, B B Webber, K G Yang, F Kutlar, A Kutlar, T H Huisma. Hb Saint Louis or alpha 2 beta 2(28)(B10)Leu----Gln in a Czechoslovakian male. Hemoglobin. vol 10. issue 6. 1987-05-20. PMID:3557999. |
hb saint louis or alpha 2 beta 2(28)(b10)leu----gln in a czechoslovakian male. |
1987-05-20 |
2023-08-11 |
Not clear |
| M Samaja, E Rovida, M Niggeler, M Perrella, L Rossi-Bernard. The dissociation of carbon monoxide from hemoglobin intermediate. The Journal of biological chemistry. vol 262. issue 10. 1987-05-15. PMID:3558353. |
the hemoglobin species investigated include hb(co)4, the diliganded symmetrical species (alpha beta-co)2 and (alpha-co beta)2, and the di- and monoliganded asymmetrical species (alpha-co beta-co)(alpha beta), (alpha-co beta)(alpha beta-co), (alpha beta-co) (alpha beta), and (alpha-co beta)(alpha beta). |
1987-05-15 |
2023-08-11 |
human |
| P J Ojwang, T Ogada, P Beris, Y Hattori, K D Lanclos, A Kutlar, F Kutlar, T H Huisma. Haplotypes and alpha globin gene analyses in sickle cell anaemia patients from Kenya. British journal of haematology. vol 65. issue 2. 1987-05-12. PMID:3828229. |
heterozygosity for the alpha-thal-2 did not affect the clinical condition nor the haematology; hb f levels were somewhat lower in ss patients with -alpha/alpha alpha than in those with alpha alpha/alpha alpha. |
1987-05-12 |
2023-08-11 |
human |
| R Kumagai, H Niitsu, I Katsura, N Nakayashiki, S Katsur. A case of a newborn infant with Hb M Iwate. The Tohoku journal of experimental medicine. vol 150. issue 3. 1987-04-08. PMID:3824377. |
one of these hbs m corresponded with hb m iwate (alpha m2 beta 2) from an adult carrier of this trait, but the other was not found in adult hemolysates. |
1987-04-08 |
2023-08-11 |
Not clear |
| R Kumagai, H Niitsu, I Katsura, N Nakayashiki, S Katsur. A case of a newborn infant with Hb M Iwate. The Tohoku journal of experimental medicine. vol 150. issue 3. 1987-04-08. PMID:3824377. |
the latter species of hb m was shown to be composed of the abnormal alpha chain and the normal gamma chain (alpha m2 gamma 2) by chain analysis, and was assumed to be specific for infants. |
1987-04-08 |
2023-08-11 |
Not clear |
| J Delanoé-Garin, Y Blouquit, N Arous, C Lacombe, W Vainchenker, J Rosa, F Galactero. Hb Kokura alpha 2 47 (CE5) Asp----Gly beta 2 in a French Jewish family. Nouvelle revue francaise d'hematologie. vol 28. issue 5. 1987-03-04. PMID:3808942. |
hb kokura alpha 2 47 (ce5) asp----gly beta 2 in a french jewish family. |
1987-03-04 |
2023-08-11 |
Not clear |