| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| K H Han, G N La Mar, K Naga. Proton magnetic resonance study of the influence of chemical modification, mutation, quaternary state, and ligation state on dynamic stability of the heme pocket in hemoglobin as reflected in the exchange of the proximal histidyl ring labile proton. Biochemistry. vol 28. issue 5. 1989-06-29. PMID:2541777. |
each modified/mutated hb exhibited kinetic subunit heterogeneity in the reduced ferrous state, with the alpha subunit exhibiting faster exchange than the beta subunit. |
1989-06-29 |
2023-08-11 |
Not clear |
| F Kutlar, L H Gu, H Hu, T H Huisma. Quantitation of hemoglobins Bart's, H, Portland-I, Portland-II and constant spring by anion-exchange high-performance liquid chromatography. Journal of chromatography. vol 487. issue 2. 1989-06-26. PMID:2722997. |
we introduce a new high-performance liquid chromatographic procedure that uses a specific anion-exchange column for the separation of hemoglobin (hb) bart's (gamma 4), hb h (beta 4), hb portland-i (zeta 2 gamma 2), hb portland-ii (zeta 2 beta 2), and the abnormal hb constant spring (alpha 2 extended beta 2) in cord blood and adult red cell lysates. |
1989-06-26 |
2023-08-11 |
Not clear |
| K Huber, G Braunitzer, D Schneeganss, J Kösters, F Grim. The primary structure of the hemoglobin of the Cormorant (Phalacrocorax carbo, Pelecaniformes). Biological chemistry Hoppe-Seyler. vol 369. issue 11. 1989-06-16. PMID:3245897. |
the erythrocytes of the adult cormorant contain two hemoglobin components in a ratio of 83% hb a to 17% hb d. the primary structures of the alpha a-, alpha d- and beta-chains are presented. |
1989-06-16 |
2023-08-11 |
human |
| B W Thanomsub, S Fucharoen, C R Brockelman, J Bhisutthibha. Effects of thalassaemic serum on the in vitro development of the malarial parasite Plasmodium falciparum. Parasitology research. vol 75. issue 3. 1989-06-08. PMID:2652138. |
schizonts of p. falciparum cultured in erythrocytes from non-thalassaemic individuals containing normal hb (alpha 2 beta 2) were also inhibited when thalassaemic serum was used in place of normal serum. |
1989-06-08 |
2023-08-11 |
Not clear |
| E C Muklwala, J Banda, S Siziya, J Atenyi, A F Fleming, D R Higg. Alpha thalassaemia in Zambian newborn. Clinical and laboratory haematology. vol 11. issue 1. 1989-06-06. PMID:2706899. |
the umbilical cord blood from 109 consecutive zambian neonates (excluding those found to be anti-hiv positive) were analysed for haemoglobin (hb) bart's and for alpha thalassaemia by restriction endonuclease analysis. |
1989-06-06 |
2023-08-11 |
Not clear |
| E C Muklwala, J Banda, S Siziya, J Atenyi, A F Fleming, D R Higg. Alpha thalassaemia in Zambian newborn. Clinical and laboratory haematology. vol 11. issue 1. 1989-06-06. PMID:2706899. |
detection of hb bart's identified all alpha-thalassaemia homozygotes (-alpha/-alpha), but fewer than 10% of heterozygotes (-alpha/alpha alpha). |
1989-06-06 |
2023-08-11 |
Not clear |
| G Massarelli, C A Scott, A Mura, F Tanda, A Coss. Hyaline bodies in Kaposi's sarcoma: an immunocytochemical and ultrastructural study. Applied pathology. vol 7. issue 1. 1989-05-30. PMID:2539847. |
paraffin sections from 45 cases of ks selected on the basis of their high content of hb were challenged with antisera against factor viiir:ag, carcinoembryonic antigen (cea), alpha-fetoprotein (afp), alpha 1-antitrypsin (a1at), fibrinogen, hemoglobin, alpha-actin and lysozyme. |
1989-05-30 |
2023-08-11 |
Not clear |
| G Falcioni, F Grelloni, G De Sanctis, P Pierani, L Felici, G V Copp. Enzymatic antioxidative defence of erythrocytes in an Italian family with Hb Volga or alpha 2 beta 2 27 (B9) Ala----Asp. Clinica chimica acta; international journal of clinical chemistry. vol 178. issue 3. 1989-05-19. PMID:3240605. |
enzymatic antioxidative defence of erythrocytes in an italian family with hb volga or alpha 2 beta 2 27 (b9) ala----asp. |
1989-05-19 |
2023-08-11 |
Not clear |
| J M Gonzalez-Redondo, T A Stoming, F Kutlar, A Kutlar, H Hu, J B Wilson, T H Huisma. Hb Monroe or alpha 2 beta 230(B12)Arg----Thr, a variant associated with beta-thalassemia due to A G----C substitution adjacent to the donor splice site of the first intron. Hemoglobin. vol 13. issue 1. 1989-05-18. PMID:2539344. |
hb monroe or alpha 2 beta 230(b12)arg----thr, a variant associated with beta-thalassemia due to a g----c substitution adjacent to the donor splice site of the first intron. |
1989-05-18 |
2023-08-11 |
Not clear |
| L Manca, B Masal. Identification of Hb J-Sardegna [alpha 50(CE8)His----Asp] by HPLC and its incidence in northern Sardinia. Hemoglobin. vol 13. issue 1. 1989-05-18. PMID:2703364. |
identification of hb j-sardegna [alpha 50(ce8)his----asp] by hplc and its incidence in northern sardinia. |
1989-05-18 |
2023-08-11 |
human |
| L Manca, B Masal. Identification of Hb J-Sardegna [alpha 50(CE8)His----Asp] by HPLC and its incidence in northern Sardinia. Hemoglobin. vol 13. issue 1. 1989-05-18. PMID:2703364. |
as many as 7,717 babies born consecutively and 3,412 blood donors of sardinian ancestry have been examined for the detection of the hb j-sardegna variant [alpha 50(ce8)his----asp]; all subjects were from northern sardinia. |
1989-05-18 |
2023-08-11 |
human |
| G Dinçol, K Dinçol, S Erde. Hb G-Coushatta or alpha 2 beta 222(B4)Glu----Ala in a Turkish male. Hemoglobin. vol 13. issue 1. 1989-05-18. PMID:2703366. |
hb g-coushatta or alpha 2 beta 222(b4)glu----ala in a turkish male. |
1989-05-18 |
2023-08-11 |
Not clear |
| J F Prior, J L Raven, J B Wilson, A Kutlar, F Kutlar, T H Huisma. Hb J-Lome or alpha 2 beta 259(E3)Lys----Asn in a Vietnamese family. Hemoglobin. vol 13. issue 1. 1989-05-18. PMID:2703367. |
hb j-lome or alpha 2 beta 259(e3)lys----asn in a vietnamese family. |
1989-05-18 |
2023-08-11 |
Not clear |
| M S Matsuura, K Fushitani, A F Rigg. The amino acid sequences of the alpha and beta chains of hemoglobin from the snake, Liophis miliaris. The Journal of biological chemistry. vol 264. issue 10. 1989-05-11. PMID:2925617. |
comparison of the sequences with those of the alpha and beta chains of human hb shows the following. |
1989-05-11 |
2023-08-11 |
human |
| L Manca, P Demuro, B Masal. Hb G-Philadelphia, or [alpha 68(E17)Asn----Lys], in north Sardinia: detection by isoelectric focusing and identification by HPLC of tryptic peptides. Clinica chimica acta; international journal of clinical chemistry. vol 177. issue 3. 1989-05-10. PMID:3233770. |
hb g-philadelphia, or [alpha 68(e17)asn----lys], in north sardinia: detection by isoelectric focusing and identification by hplc of tryptic peptides. |
1989-05-10 |
2023-08-11 |
Not clear |
| L Manca, P Demuro, B Masal. Hb G-Philadelphia, or [alpha 68(E17)Asn----Lys], in north Sardinia: detection by isoelectric focusing and identification by HPLC of tryptic peptides. Clinica chimica acta; international journal of clinical chemistry. vol 177. issue 3. 1989-05-10. PMID:3233770. |
11,129 individuals of the northern area of the island of sardinia (7,717 newborns and 3,412 adults) were examined for the hb g-philadelphia variant [alpha 68(e17)asn----lys]. |
1989-05-10 |
2023-08-11 |
Not clear |
| F Iu Nasyrova, A M Mirakilova, I B Ryzhova, R B Sabzanova, S A Limborskai. [Heterogeneity of globin protein synthesis in bone marrow cells of patients with homozygous beta-thalassemia from Tadzhikistan]. Molekuliarnaia genetika, mikrobiologiia i virusologiia. issue 10. 1989-04-17. PMID:2976480. |
homozygous beta-thalassemic cases with low content of hb f in blood cells (5-10%), with substantial disbalance of alpha and beta-globin synthesis and marked production of gamma-globins in bone marrow cells and in blood reticulocytes are of special interest. |
1989-04-17 |
2023-08-11 |
Not clear |
| J M Gonzalez-Redondo, J C Diaz-Chico, J J Malcorra-Azpiazu, M I Balda-Aguirre, T H Huisma. Characterization of a newly discovered alpha-thalassaemia-1 in two Spanish patients with Hb H disease. British journal of haematology. vol 70. issue 4. 1989-03-21. PMID:3219296. |
a new deletion of more than 27 kb, removing the psi zeta 1, psi alpha 2, psi alpha 1, alpha 2, alpha 1 and theta 1 globin genes has been found in four members of a spanish family, including two patients with hb h disease. |
1989-03-21 |
2023-08-11 |
Not clear |
| J G Gilma. Expression of G gamma and A gamma globin genes in human adults. Hemoglobin. vol 12. issue 5-6. 1989-02-16. PMID:2463237. |
expression of the human fetal g gamma and a gamma globin genes declines shortly after birth, and adults generally have less than 1% fetal hemoglobin or hb f (alpha 2 gamma 2). |
1989-02-16 |
2023-08-11 |
human |
| Y T Zeng, S Z Huang, M J Che. The types and distribution of alpha-thalassemia-2 in China. Hemoglobin. vol 12. issue 5-6. 1989-02-16. PMID:3209388. |
the results showed that 76 cases (68.5%) were of the deletion type, eight cases (7.2%) had hb constant spring (hb cs), and 27 cases (24.3%) were of the nondeletion and hb cs types (alpha t). |
1989-02-16 |
2023-08-11 |
Not clear |