| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| M A Zago, F F Costa, C Bottur. Thalassaemia intermedia in a family with beta 0-thalassaemia and Hb Hasharon. Journal of medical genetics. vol 19. issue 6. 1983-03-17. PMID:7154040. |
globin chain synthesis in reticulocytes showed non-alpha/total alpha ratios of 0.29, 0.39, and 0.73 respectively for the patient, the mother, and the father, who is heterozygous for both the beta 0-thalassemia and hb hasharon genes. |
1983-03-17 |
2023-08-12 |
Not clear |
| J T de Araujo, V S Ribeiro, M S Costa Silva, J C De Bonis, R A de Arauj. [Hemoglobin E alpha 2 beta 2(26) glutamic-lysine (Hb E alpha 2 beta 2(26) Glu replaced by Lys)]. Revista do Instituto de Medicina Tropical de Sao Paulo. vol 24. issue 4. 1983-03-17. PMID:7156704. |
[hemoglobin e alpha 2 beta 2(26) glutamic-lysine (hb e alpha 2 beta 2(26) glu replaced by lys)]. |
1983-03-17 |
2023-08-12 |
Not clear |
| H F Bunn, C T Noguchi, J Hofrichter, G P Schechter, A N Schechter, W A Eato. Molecular and cellular pathogenesis of hemoglobin SC disease. Proceedings of the National Academy of Sciences of the United States of America. vol 79. issue 23. 1983-03-11. PMID:6961429. |
the polymerization of deoxygenated mixtures containing sickle cell hb (hb s; alpha 2 beta 2(6)glu leads to val) and hb c (alpha 2 beta 2(6)glu leads to lys) was investigated by measurements of delay times and solubilities. |
1983-03-11 |
2023-08-12 |
Not clear |
| W F Moo-Penn, D L Jue, M H Johnson, J E McGuffey, H Simpkins, J Kat. Hemoglobin Queens: alpha 34 (B15) Leu-Arg structural and functional properties and its association with Hb E. American journal of hematology. vol 13. issue 4. 1983-03-11. PMID:7158628. |
hemoglobin queens: alpha 34 (b15) leu-arg structural and functional properties and its association with hb e. hemoglobin queens: alpha 34 (b15) leu-arg was found in association with hb e in a vietnamese boy. |
1983-03-11 |
2023-08-12 |
Not clear |
| M Sinet, B Bohn, P Guesnon, C Poyar. Temperature independence of the alkaline Bohr effect in pig red cells and pig haemoglobin solutions. Biochimica et biophysica acta. vol 708. issue 2. 1983-02-14. PMID:7171612. |
conversely, the temperature dependence of the alkaline bohr effect of hb a0 should be related to the oxygen-linked binding of c1- at the alpha 1-alpha 2 interface. |
1983-02-14 |
2023-08-12 |
human |
| Y Kawamura, H Hasumi, S Nakamur. Kinetic studies on the reconstitution of deoxyhemoglobin from isolated alpha and beta chains. Journal of biochemistry. vol 92. issue 4. 1983-02-14. PMID:7174642. |
the reconstitution reaction of deoxy hemoglobin (hb) tetramer from isolated alpha and beta chains was kinetically studied by measuring circular dichroism (cd) changes in the soret and the ultraviolet regions and optical absorbance change in the soret region with a stopped-flow apparatus. |
1983-02-14 |
2023-08-12 |
Not clear |
| Y Kawamura, H Hasumi, S Nakamur. Kinetic studies on the reconstitution of deoxyhemoglobin from isolated alpha and beta chains. Journal of biochemistry. vol 92. issue 4. 1983-02-14. PMID:7174642. |
on the other hand, the cd change in the ultraviolet region was ascribed to the combination of two alpha beta dimers into an hb tetramer. |
1983-02-14 |
2023-08-12 |
Not clear |
| T Harano, K Harano, S Shibata, S Ueda, K Imai, M Sek. HB Handa [alpha 90 (FG 2) Lys replaced by Met]: structure and biosynthesis of a new slightly higher oxygen affinity variant. Hemoglobin. vol 6. issue 4. 1983-01-19. PMID:6815131. |
hb handa [alpha 90 (fg 2) lys replaced by met]: structure and biosynthesis of a new slightly higher oxygen affinity variant. |
1983-01-19 |
2023-08-12 |
Not clear |
| G V Sciarratta, G Sansone, M Valbonesi, J B Wilson, H Lam, B B Webber, M E Headlee, T H Huisma. Hb Cheverly or alpha 2 beta 2 45(CD4)Phe replaced by Ser in an elderly Italian male. Hemoglobin. vol 6. issue 4. 1983-01-19. PMID:6815132. |
hb cheverly or alpha 2 beta 2 45(cd4)phe replaced by ser in an elderly italian male. |
1983-01-19 |
2023-08-12 |
Not clear |
| Z Yi-Tao, M E Headlee, J Henson, H Lam, J B Wilson, T H Huisma. Identification of hemoglobin G-Philadelphia (alpha 68 Asn replaced by Lys) and hemoglobin Matsue-Oki (alpha 75 Asp replaced by Asn) in a black infant. Biochimica et biophysica acta. vol 707. issue 2. 1983-01-07. PMID:6814490. |
the amino acid substitutions in hb g-philadelphia and hb matsue-oki are located in the tryptic peptide alpha t-9, which is 29 amino acid residues long. |
1983-01-07 |
2023-08-12 |
Not clear |
| Z Yi-Tao, M E Headlee, J Henson, H Lam, J B Wilson, T H Huisma. Identification of hemoglobin G-Philadelphia (alpha 68 Asn replaced by Lys) and hemoglobin Matsue-Oki (alpha 75 Asp replaced by Asn) in a black infant. Biochimica et biophysica acta. vol 707. issue 2. 1983-01-07. PMID:6814490. |
although the alpha 68 asn replaced by lys substitution is readily demonstrable in hb g-philadelphia the elucidation of the alpha 75 asp replaced by asn replacement in hb matsue-oki was greatly facilitated by the use of these microprocedures. |
1983-01-07 |
2023-08-12 |
Not clear |
| M Sellaye, Y Blouquit, F Galacteros, N Arous, N Monplaisir, M D Rhoda, F Braconnier, J Ros. A new silent hemoglobin variant in a black family from French West Indies, hemoglobin Le Lamentin alpha 20 His replaced by Gln. FEBS letters. vol 145. issue 1. 1982-12-21. PMID:7128817. |
a new abnormal hemoglobin hb le lamentin alpha 20 (b1) his replaced by gln was discovered during a survey of cord blood from the french west indies (martinique). |
1982-12-21 |
2023-08-12 |
Not clear |
| M L Salkie, P A Gordon, W M Rigal, H Lam, J B Wilson, M E Headlee, T H Huisma. Hb A2-Canada or alpha 2 delta 2 99(G1) Asp replaced by Asn, a newly discovered delta chain variant with increased oxygen affinity occurring in cis to beta-thalassemia. Hemoglobin. vol 6. issue 3. 1982-12-18. PMID:7129931. |
hb a2-canada or alpha 2 delta 2 99(g1) asp replaced by asn, a newly discovered delta chain variant with increased oxygen affinity occurring in cis to beta-thalassemia. |
1982-12-18 |
2023-08-12 |
Not clear |
| M L Salkie, P A Gordon, W M Rigal, H Lam, J B Wilson, M E Headlee, T H Huisma. Hb A2-Canada or alpha 2 delta 2 99(G1) Asp replaced by Asn, a newly discovered delta chain variant with increased oxygen affinity occurring in cis to beta-thalassemia. Hemoglobin. vol 6. issue 3. 1982-12-18. PMID:7129931. |
a similar substitution has been found in the beta chain of hb kempsey (alpha 2 beta 2 99 asp replaced by asn). |
1982-12-18 |
2023-08-12 |
Not clear |
| C Y Ip, T Asakura, K Adach. Polymerization of carbamylated deoxyhemoglobin S in concentrated phosphate buffer. The Journal of biological chemistry. vol 257. issue 21. 1982-12-18. PMID:7130183. |
to study the effect of carbamylation on the polymerization of deoxyhemoglobin (hb) s, three types of nh2-terminal-carbamylated hb s specifically modified at the nh2 termini at the alpha, beta, or all four subunit chains, alpha c2 beta sc2, and alpha 2 beta sc2, and epsilon-lysine-carbamylated hb s were prepared by reacting hb s with cyanate. |
1982-12-18 |
2023-08-12 |
Not clear |
| J Pagnier, J Elion, C Lapouméroulie, C Vigneron, D Labi. Homozygous deletional alpha + thalassaemia associated with unequal expression of the two remaining alpha 1 genes (alpha 1A and alpha 1Q). British journal of haematology. vol 52. issue 1. 1982-12-03. PMID:7115621. |
a cambodian family presenting several haemoglobinopathies, hb e, hb q and alpha + thalassaemia, has been investigated. |
1982-12-03 |
2023-08-12 |
Not clear |
| V S Sharma, M E John, M R Waterma. Functional studies on hemoglobin opossum. Conclusions drawn regarding the role of the distal histidine. The Journal of biological chemistry. vol 257. issue 20. 1982-12-03. PMID:7118915. |
comparison of kinetic studies of opossum hemoglobin with normal human hemoglobin shows that alpha chains in hb opossum, despite the lack of distal histidine, do not differ significantly in co-combination rates in either the t or r states. |
1982-12-03 |
2023-08-12 |
human |
| D M Hunt, D R Higgs, P Winichagoon, J B Clegg, D J Weatheral. Haemoglobin Constant Spring has an unstable alpha chain messenger RNA. British journal of haematology. vol 51. issue 3. 1982-10-12. PMID:7104225. |
haemoglobin constant spring (hb cs) is a variant with an elongated alpha-chain associated with an alpha + thalassaemia phenotype. |
1982-10-12 |
2023-08-12 |
Not clear |
| D M Hunt, D R Higgs, P Winichagoon, J B Clegg, D J Weatheral. Haemoglobin Constant Spring has an unstable alpha chain messenger RNA. British journal of haematology. vol 51. issue 3. 1982-10-12. PMID:7104225. |
the amount of alpha mrna relative to beta mrna in reticulocytes was reduced in carriers of hb cs by an amount equivalent to the reduction observed in carriers of alpha + thalassaemia. |
1982-10-12 |
2023-08-12 |
Not clear |
| J M Friedman, R A Stepnoski, M Stavola, M R Ondrias, R L Con. Ligation and quaternary structure induced changes in the heme pocket of hemoglobin: a transient resonance Raman study. Biochemistry. vol 21. issue 9. 1982-09-10. PMID:7093226. |
with respect to the structural parameter responsible for variations in the pi orbital electron density of the porphyrin, the degree of alteration of the heme pocket configuration relative to deoxy-hb(t) follows the sequence: liganded hb(r) greater than liganded hb(r) + ihp greater than liganded hb(t) [alpha chain greater than beta chain] greater than deoxy-hb(r). |
1982-09-10 |
2023-08-12 |
Not clear |