| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| H Frischer, J Bowma. Hemoglobin E, an oxidatively unstable mutation. The Journal of laboratory and clinical medicine. vol 85. issue 4. 1975-06-26. PMID:1120926. |
hemoglobin e is an oxidatively unstable hemoglobin, possibly with weakened alpha 1 beta 1 contact; it may result in increased susceptibility to oxidative hemolysis and can be simply detected and differentiated from both hb c and hb o-arabia. |
1975-06-26 |
2023-08-11 |
Not clear |
| H H Kazazian, G D Ginder, P G Snyder, R J Van Beneden, A P Woodhea. Further evidence of a quantitative deficiency of chain-specific globin mRNA in the thalassemia syndromes. Proceedings of the National Academy of Sciences of the United States of America. vol 72. issue 2. 1975-06-25. PMID:1054838. |
in contrast to individuals with either hemolytic anemia without hemoglobinopathy or sickle cell anemia who had beta mrna to alpha mrna ratios of approximately one, a patient with hb s-beta-thalassemia had a ratio of beta mrna to alpha mrna of 0.75 while two subjects with homozygous beta-thalassemia had severe deficiencies of beta mrna. |
1975-06-25 |
2023-08-11 |
human |
| H H Kazazian, G D Ginder, P G Snyder, R J Van Beneden, A P Woodhea. Further evidence of a quantitative deficiency of chain-specific globin mRNA in the thalassemia syndromes. Proceedings of the National Academy of Sciences of the United States of America. vol 72. issue 2. 1975-06-25. PMID:1054838. |
conversely, a patient with alpha-thalassemia (hb h disease) had a ratio of beta mrna to alpha mrna on reticulocyte polyribosomes of 6. |
1975-06-25 |
2023-08-11 |
human |
| A Mauran, B Manesse, M Cohen-Solal, M C Garel, J Thillet, Y Blouquit, J Caburi, H Vergne, J Ros. [Clinical and biochemical studies of a new case of Hb J Baltimore (alpha 2A beta2 16 Gly yields Asp) isolated in France (author's transl)]. Nouvelle revue francaise d'hematologie. vol 14. issue 5. 1975-06-09. PMID:4141765. |
[clinical and biochemical studies of a new case of hb j baltimore (alpha 2a beta2 16 gly yields asp) isolated in france (author's transl)]. |
1975-06-09 |
2023-08-11 |
Not clear |
| A O Cavdar, A Arcaso. Hb D punjab--alpha thalassaemia combination in a Turkish family. Scandinavian journal of haematology. vol 13. issue 4. 1975-04-08. PMID:4445829. |
hb d punjab--alpha thalassaemia combination in a turkish family. |
1975-04-08 |
2023-08-11 |
Not clear |
| C C Kennedy, G Blundell, P A Lorkin, A Lang, H Lehman. Haemoglobin Belfast 15 (A12) tryptophan leading to arginine: a new unstable haemoglobin variant. British medical journal. vol 4. issue 5940. 1975-03-10. PMID:4434089. |
a new unstable haemoglobin, alpha(2)beta(2)15 trp--> arg (hb belfast), with increased oxygen affinity has been found during the routine investigation of a long-stay psychiatric patient. |
1975-03-10 |
2023-08-11 |
Not clear |
| H Brunner, A Mayer, K Gersonde, K Winterhalte. A resonance Raman study on Hb M Iwate (alpha87His leads to Tyr beta)2, and Hb Zürich (alpha beta 63 His-Arg). 2. FEBS letters. vol 48. issue 1. 1975-02-18. PMID:4430367. |
a resonance raman study on hb m iwate (alpha87his leads to tyr beta)2, and hb zürich (alpha beta 63 his-arg). |
1975-02-18 |
2023-08-11 |
Not clear |
| J Thillet, J Caburi, B Brun, M Cohen-Solal, M C Garel, M N Minh, J Ros. Abnormal functional properties of Hb Hope alpha C2A beta2 (H14) Gly-Asp: a low oxygen affinity hemoglobin with decreased DPG effect. FEBS letters. vol 47. issue 1. 1975-01-27. PMID:4426396. |
abnormal functional properties of hb hope alpha c2a beta2 (h14) gly-asp: a low oxygen affinity hemoglobin with decreased dpg effect. |
1975-01-27 |
2023-08-11 |
Not clear |
| M C Garel, M Cohen-Solal, Y Blouquit, J Ros. A method for isolation of abnormal haemoglobins with high oxygen affinity due to a frozen quaternary r-structure: application to Hb Creteil alpha 2 A beta 2 (F5) 89 ASN. FEBS letters. vol 43. issue 1. 1974-11-07. PMID:4850219. |
a method for isolation of abnormal haemoglobins with high oxygen affinity due to a frozen quaternary r-structure: application to hb creteil alpha 2 a beta 2 (f5) 89 asn. |
1974-11-07 |
2023-08-11 |
Not clear |
| R Benesch, R E Benesch, S Yun. Chemical modifications that inhibit gelation of sickle hemoglobin. Proceedings of the National Academy of Sciences of the United States of America. vol 71. issue 4. 1974-07-31. PMID:4524653. |
the increase in minimum gelling concentration of hb s that results from modification of the alpha n-termini is the same as that produced by dilution of hb s with an equal amount of hb a. |
1974-07-31 |
2023-08-11 |
Not clear |
| S R Hollán, J G Szelenyi, G Brimhall, M Duerst, R T Jones, R D Koler, Z Stockle. Multiple alpha chain loci for human haemoglobins: Hb J-Buda and Hb G-Pest. Nature. vol 235. issue 5332. 1972-03-30. PMID:4550395. |
multiple alpha chain loci for human haemoglobins: hb j-buda and hb g-pest. |
1972-03-30 |
2023-08-11 |
human |
| R K Abramson, D L Rucknagel, D C Shreffler, J J Saav. Homozygous Hb J Tongariki: evidence for only one alpha chain structural locus in Melanesians. Science (New York, N.Y.). vol 169. issue 3941. 1970-08-26. PMID:5427353. |
homozygous hb j tongariki: evidence for only one alpha chain structural locus in melanesians. |
1970-08-26 |
2023-08-11 |
Not clear |
| R K Abramson, D L Rucknagel, D C Shreffler, J J Saav. Homozygous Hb J Tongariki: evidence for only one alpha chain structural locus in Melanesians. Science (New York, N.Y.). vol 169. issue 3941. 1970-08-26. PMID:5427353. |
a high frequency of hb j tongariki (alpha 115 ala --> asp) was found in a kilenge village in new britain. |
1970-08-26 |
2023-08-11 |
Not clear |
| E W Bau. Hb alpha 2glu beta 2 (Hb I) in a Caucasian family: independent mutation of common origin? Humangenetik. vol 6. issue 4. 1969-07-03. PMID:5713622. |
hb alpha 2glu beta 2 (hb i) in a caucasian family: independent mutation of common origin? |
1969-07-03 |
2023-08-12 |
Not clear |
| W Ostertag, E W Smit. Hb Sinai, a new alpha chain mutant alpha his 47. Humangenetik. vol 6. issue 4. 1969-07-03. PMID:5713624. |
hb sinai, a new alpha chain mutant alpha his 47. |
1969-07-03 |
2023-08-12 |
Not clear |
| J F Bertles, T A Borges. Disproportional synthesis of the adult duck's two hemoglobins during acute anemia. The Journal of clinical investigation. vol 47. issue 3. 1968-04-10. PMID:5637150. |
duck erythrocytes produced in response to acutely induced anemic hypoxia (hemolysis or blood loss) contained reciprocally altered proportions of hb i (alpha(2) (i) beta(2) (i)) and hb ii (alpha(2) (ii) beta(2) (ii)); the relative proportion of hb ii was 50-100% increased. |
1968-04-10 |
2023-08-11 |
human |
| A Fantoni, A Bank, P A Mark. Globin composition and synthesis of hemoglobins in developing fetal mice erythroid cells. Science (New York, N.Y.). vol 157. issue 3794. 1967-10-22. PMID:6039000. |
hb e(i) has x- and y-globin chains; hb e(ii) has alpha and y; hb e(iii), alpha and z. |
1967-10-22 |
2023-08-12 |
mouse |
| J B Clegg, M A Naughton, D J Weatherbal. Abnormal human haemoglobins. Separation and characterization of the alpha and beta chains by chromatography, and the determination of two new variants, hb Chesapeak and hb J (Bangkok). Journal of molecular biology. vol 19. issue 1. 1967-08-08. PMID:5967288. |
separation and characterization of the alpha and beta chains by chromatography, and the determination of two new variants, hb chesapeak and hb j (bangkok). |
1967-08-08 |
2023-08-12 |
human |