| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| J G Szelényi, M Horányi, J Földi, J Hudacsek, L István, S R Hollá. A new hemoblogin variant in hungary: Hb Savaria - alpha 49 (CE7) Ser replace by Arg. Hemoglobin. vol 4. issue 1. 1980-04-26. PMID:7353957. |
a new hemoblogin variant in hungary: hb savaria - alpha 49 (ce7) ser replace by arg. |
1980-04-26 |
2023-08-12 |
Not clear |
| J G Szelényi, M Horányi, J Földi, J Hudacsek, L István, S R Hollá. A new hemoblogin variant in hungary: Hb Savaria - alpha 49 (CE7) Ser replace by Arg. Hemoglobin. vol 4. issue 1. 1980-04-26. PMID:7353957. |
the abnormal component amounted to about 30% and proved to be a new hemoglobin variant, alpha 49 (ce7) ser replaced by arg, which has been named hb savaria. |
1980-04-26 |
2023-08-12 |
Not clear |
| M B Smith, M N Cauch. Quantitative studies of Hb Bart's levels and red cell indices in alpha thalassaemia trait in Mediterraneans. Pathology. vol 11. issue 4. 1980-04-23. PMID:530752. |
quantitative studies of hb bart's levels and red cell indices in alpha thalassaemia trait in mediterraneans. |
1980-04-23 |
2023-08-11 |
Not clear |
| V Avikainen, K Willman, P Rokkane. Stress hormones, lipids, and factors of hemostasis in trauma patients with and without fat embolism syndrome: a comparative study at least one year after severe trauma. The Journal of trauma. vol 20. issue 2. 1980-04-23. PMID:7354496. |
the following were measured: blood hb, leucocytes, platelets, protein and lipid electrophoresis, acth, cortisol, tsh, gh, insulin, glucose, nefa, certain coagulation and fibrinolytic studies, alpha 1 antitrypsin, and antithrombin iii. |
1980-04-23 |
2023-08-12 |
Not clear |
| S C Wong, M A Al. Laboratory diagnosis of HB CC-alpha-thalassemia. Clinical biochemistry. vol 12. issue 5. 1980-03-27. PMID:519845. |
routine laboratory investigations of hemoglobinopathies include hb electrophoresis for abnormal hemoglobins, determination of hb a2 (alpha 2 delta 2) for beta-thalassemia traits, staining for hb h (beta 4) inclusions for alpha-thalassemia traits and estimation of hb f (alpha 2 lambda 2) for the presence of hereditary persistence of fetal hemoglobin genes (hpfh). |
1980-03-27 |
2023-08-11 |
Not clear |
| S Musumeci, G Schilirò, G Pizzarelli, L Tentori, M Marinucci, P P Fontanarosa, G Russ. Hemoglobin G San José [beta 2 7 (A4) Glu to Gly alpha 2], beta thalassemia, and alpha thalassemia in a Sicilian family. Human genetics. vol 52. issue 2. 1980-02-28. PMID:511180. |
therefore, the possibility of coexistence of an alpha thalassemia trait with a beta thalassemia trait in the mother of the proposita and with hb g san josé heterozygosity in the two sisters who had lowered levels of abnormal hb is discussed. |
1980-02-28 |
2023-08-11 |
Not clear |
| H Sick, K Gersond. Co-binding studies on Hb M Iwate. Allostery of a T state haemoglobin. Biochimica et biophysica acta. vol 581. issue 1. 1980-02-15. PMID:41591. |
the mutant haemoglobin hb m iwate alpha 2mmet87his leads to tyr beta 2, is characterized by a stable t structure and a low ligand affinity. |
1980-02-15 |
2023-08-11 |
Not clear |
| R M Baine, J M Wright, R W Wilkinso. HB G Waimanalo (alpha 64 Asp replaced by Asn) in a child with homozygous beta-thalassemia. Hemoglobin. vol 3. issue 4. 1980-01-24. PMID:500373. |
hb g waimanalo (alpha 64 asp replaced by asn) in a child with homozygous beta-thalassemia. |
1980-01-24 |
2023-08-11 |
Not clear |
| M Marinucci, F Mavilio, P P Fontanarosa, L Tentori, C Brancat. Studies on a family with Hb J Calabria (alpha 2 beta 2 64 (E8) Gly replaced by Asp). Hemoglobin. vol 3. issue 5. 1980-01-24. PMID:500375. |
studies on a family with hb j calabria (alpha 2 beta 2 64 (e8) gly replaced by asp). |
1980-01-24 |
2023-08-11 |
human |
| S Musumeci, G Schiliro, G Pizzarelli, A D'Agata, A Fischer, G Russ. Alpha thalassaemia in Sicily: haematological and biosynthetic studies. British journal of haematology. vol 43. issue 3. 1980-01-19. PMID:497118. |
the standard haematological tests and the alpha/beta chain synthesis ratios showed significantly different results in the patients with hb h disease as compared with alpha thalassaemia carriers, except for hb a2 values. |
1980-01-19 |
2023-08-11 |
Not clear |
| S Musumeci, G Schiliro, G Pizzarelli, A D'Agata, A Fischer, G Russ. Alpha thalassaemia in Sicily: haematological and biosynthetic studies. British journal of haematology. vol 43. issue 3. 1980-01-19. PMID:497118. |
there was no significant difference in the mean rbc, mcv, hb a2, hb a1 and hb f of alpha thalassaemia carriers compared with normal controls. |
1980-01-19 |
2023-08-11 |
Not clear |
| S T Olson, V Massey, S Ghisla, C D Whitfiel. Suicide inactivation of the flavoenzyme D-lactate dehydrogenase by alpha-hydroxybutynoate. Biochemistry. vol 18. issue 21. 1980-01-19. PMID:497163. |
the acetylenic alpha-hydroxy acid 2-hydroxy-3-butynoate (alpha hb) is a substrate and an irreversible inactivator of the fad-containing flavoenzyme d-lactate dehydrogenase from megasphaera elsdenii. |
1980-01-19 |
2023-08-11 |
Not clear |
| S T Olson, V Massey, S Ghisla, C D Whitfiel. Suicide inactivation of the flavoenzyme D-lactate dehydrogenase by alpha-hydroxybutynoate. Biochemistry. vol 18. issue 21. 1980-01-19. PMID:497163. |
on the average, the enzyme undergoes five catalytic turnovers with alpha hb in air at ph 7.0 before being inactivated. |
1980-01-19 |
2023-08-11 |
Not clear |
| S T Olson, V Massey, S Ghisla, C D Whitfiel. Suicide inactivation of the flavoenzyme D-lactate dehydrogenase by alpha-hydroxybutynoate. Biochemistry. vol 18. issue 21. 1980-01-19. PMID:497163. |
experiments were conducted to test whether inactivation was initiated by an alpha hb allene carbanion or the dehydrogenation product of alpha hb. |
1980-01-19 |
2023-08-11 |
Not clear |
| S T Olson, V Massey, S Ghisla, C D Whitfiel. Suicide inactivation of the flavoenzyme D-lactate dehydrogenase by alpha-hydroxybutynoate. Biochemistry. vol 18. issue 21. 1980-01-19. PMID:497163. |
since the keto acid derived from the oxidation of this alpha-hydroxy acid is expected to be as reactive as 2-keto-3-butynoate, it is concluded that an allene carbanion produced by abstraction of the alpha-hydrogen of alpha hb is the reactive species which covalently adds to the flavin. |
1980-01-19 |
2023-08-11 |
Not clear |
| M Marinucci, F Mavilio, A Massa, M Gabbianelli, P P Fontanarosa, A Camagna, C Ignesti, L Tentor. A new abnormal human hemoglobin: Hb Prato (alpha 2 31 (B12) Arg leads to Ser beta 2). Biochimica et biophysica acta. vol 578. issue 2. 1979-12-18. PMID:486536. |
a new abnormal human hemoglobin: hb prato (alpha 2 31 (b12) arg leads to ser beta 2). |
1979-12-18 |
2023-08-11 |
human |
| J Thillet, M L North, J Ros. Functional properties of Hb Stanleyville II alpha 78 (EF 7) asparagine replaced by lysine. Effect of sodium chloride. Hemoglobin. vol 3. issue 2-3. 1979-11-21. PMID:39047. |
functional properties of hb stanleyville ii alpha 78 (ef 7) asparagine replaced by lysine. |
1979-11-21 |
2023-08-11 |
Not clear |
| B Dingle, H Farguharson, D Williams, J B Wilson, T H Huisma. Hb Rainier or alpha 2 beta 2 (145 (HC2) Tyr replaced by Cys) observed in members of a Canadian family of Greek origin. Hemoglobin. vol 3. issue 2-3. 1979-11-21. PMID:478981. |
hb rainier or alpha 2 beta 2 (145 (hc2) tyr replaced by cys) observed in members of a canadian family of greek origin. |
1979-11-21 |
2023-08-11 |
Not clear |
| R E Benesch, S Kwong, R Edalji, R Benesc. alpha Chain mutations with opposite effects on the gelation of hemoglobin S. The Journal of biological chemistry. vol 254. issue 17. 1979-10-26. PMID:468817. |
by contrast, the introduction of a tyrosine at alpha 75 and an alanine at alpha 6 have the opposite effect and are the first examples of alpha chain mutations which potentiate the gelation of hb s. the molecular mechanisms responsible for the effects of the mutations on the self-association of hb s are discussed. |
1979-10-26 |
2023-08-11 |
Not clear |
| T H Huisma. Sickle cell anemia as a syndrome: a review of diagnostic features. American journal of hematology. vol 6. issue 2. 1979-10-24. PMID:382840. |
combinations of a hb s heterozygosity with a heterozygosity for a hb d-type of variant, for either one of two types of beta-thalassemia, two types of alpha beta- thalassemia, and five types of hpfh are discussed, and data are compared with those obtained for hb s homozygotes. |
1979-10-24 |
2023-08-11 |
Not clear |