| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| T Nakatsuji, H Lam, T H Huisma. Hb F-Calluna or alpha 2 gamma 2(12 Thr replaced by Arg; 75Ile; 136Ala) in a Caucasian baby. Hemoglobin. vol 7. issue 6. 1984-04-03. PMID:6199326. |
hb f-calluna or alpha 2 gamma 2(12 thr replaced by arg; 75ile; 136ala) in a caucasian baby. |
1984-04-03 |
2023-08-12 |
Not clear |
| T Nakatsuji, B B Webber, S E Johnson, T H Huisma. Two rare alpha chain variants, Hb Dunn or alpha 26(A4)Asp replaced by Asn beta 2 and Hb G-Pest or alpha 274(EF3)Asp replaced by Asn beta 2, observed in an Indian and a black newborn. Hemoglobin. vol 7. issue 6. 1984-04-03. PMID:6668192. |
two rare alpha chain variants, hb dunn or alpha 26(a4)asp replaced by asn beta 2 and hb g-pest or alpha 274(ef3)asp replaced by asn beta 2, observed in an indian and a black newborn. |
1984-04-03 |
2023-08-12 |
Not clear |
| F Morle, P Jaccoud, E Dorleac, M Motta, J Delaunay, J Gode. Alpha-globin gene deletions associated with alpha A and alpha G Philadelphia in an Algerian family that includes two Hb G homozygotes. Human genetics. vol 65. issue 3. 1984-03-30. PMID:6199285. |
alpha-globin gene deletions associated with alpha a and alpha g philadelphia in an algerian family that includes two hb g homozygotes. |
1984-03-30 |
2023-08-12 |
human |
| F Morle, P Jaccoud, E Dorleac, M Motta, J Delaunay, J Gode. Alpha-globin gene deletions associated with alpha A and alpha G Philadelphia in an Algerian family that includes two Hb G homozygotes. Human genetics. vol 65. issue 3. 1984-03-30. PMID:6199285. |
in subjects with genotype (-alpha a/-alpha g) or (-alpha g/-alpha g), the output of the remaining alpha genes is sufficiently high to avoid the appearance of hb h. this situation contrasts with that reported in an algerian patient, who had a (-alpha a/-alpha a) genotype but who was producing hb h (whitelaw et al. |
1984-03-30 |
2023-08-12 |
human |
| J Rochette, C Poyart, B Varet, H Wajcma. A new hemoglobin variant altering the alpha 1 beta 2 contact: Hb Chemilly alpha 2 beta 2 99(G1)Asp leads to Val. FEBS letters. vol 166. issue 1. 1984-03-06. PMID:6692925. |
a new hemoglobin variant altering the alpha 1 beta 2 contact: hb chemilly alpha 2 beta 2 99(g1)asp leads to val. |
1984-03-06 |
2023-08-12 |
Not clear |
| C J Bruzdzinski, K L Sisco, S J Ferrucci, D L Rucknage. The occurrence of the alpha G-Philadelphia-globin allele on a double-locus chromosome. American journal of human genetics. vol 36. issue 1. 1984-03-05. PMID:6198906. |
restriction analyses published thus far have shown that among persons with 30% and 40% hemoglobin (hb) g the alpha g allele is seen only in a single-locus haplotype. |
1984-03-05 |
2023-08-12 |
Not clear |
| A Brzozowski, Z Derewenda, E Dodson, G Dodson, M Grabowski, R Liddington, T Skarzyński, D Vallel. Bonding of molecular oxygen to T state human haemoglobin. Nature. vol 307. issue 5946. 1984-02-23. PMID:6690986. |
we report here the crystal structure of t state human hb in which the alpha chains are oxygenated and the beta subunits are oxygen-free. |
1984-02-23 |
2023-08-12 |
human |
| R Galanello, M Pirastu, M A Melis, E Paglietti, P Moi, A Ca. Phenotype-genotype correlation in haemoglobin H disease in childhood. Journal of medical genetics. vol 20. issue 6. 1984-02-14. PMID:6317863. |
these results suggest that in those hb h disease patients with the non-deletion [(alpha alpha)th] determinant, two alpha globin genes produce fewer alpha globin chains than a single alpha globin locus. |
1984-02-14 |
2023-08-12 |
Not clear |
| H Adachi, T Asakura, K Adach. Effect of chloride ion on the oxygen affinity of hemoglobin York (alpha 2 beta 2(146)Pro) and S-York hybrid hemoglobin (alpha 2 beta S beta York). Role of the beta 82 lysyl and beta 146 histydyl residues in chloride binding to hemoglobin. The Journal of biological chemistry. vol 258. issue 22. 1984-01-07. PMID:6417128. |
we estimated the relative role of various chloride binding sites in determining the oxygen affinity of hemoglobin using abnormal hemoglobins such as hb york (hb y) (alpha 2 beta 2(146)pro), hb malmö (hb m) (alpha 2 beta 2(97)gln), and hb s and chemically modified hemoglobins such as cross-linked hb s, hb y, and asymmetrical sy hemoglobin with bis(3,5-dibromosalicyl)fumarate. |
1984-01-07 |
2023-08-12 |
Not clear |
| E C Abraham, M Stallings, A Abraham, M M Elseweid. Affinity chromatographic quantitation of glycosylated hemoglobin in newborn infants. Hemoglobin. vol 7. issue 5. 1983-12-20. PMID:6195129. |
rechromatography of the glyco and nonglyco hb fractions on bio-rex 70 columns indicated that hb fo-like glyco hb (presumably formed by glycosylation of the alpha chain amino terminus and epsilon-amino groups of lysyl amino acids) constituted about 60% of the glyco hb fraction, whereas both hb fic and hb fia+b components contained only small portions of the glyco hb. |
1983-12-20 |
2023-08-12 |
Not clear |
| C Romero Garcia, J L Navarro, H Lam, B B Webber, M G Headlee, J B Wilson, T H Huisma. Hb A2-Manzanares or alpha 2 delta 2 121 (GH4) Glu replaced by Val, an unstable delta chain variant observed in a Spanish family. Hemoglobin. vol 7. issue 5. 1983-12-20. PMID:6629825. |
hb a2-manzanares or alpha 2 delta 2 121 (gh4) glu replaced by val, an unstable delta chain variant observed in a spanish family. |
1983-12-20 |
2023-08-12 |
Not clear |
| D Juricic, I Crepinko, G D Efremov, H Lam, B B Webber, M G Headlee, T H Huisma. Hb A2-Zagreb or alpha 2 delta 2(125)(H3)Gln replaced by Glu, a new delta chain variant in association with delta beta-thalassemia. Hemoglobin. vol 7. issue 5. 1983-12-20. PMID:6629826. |
hb a2-zagreb or alpha 2 delta 2(125)(h3)gln replaced by glu, a new delta chain variant in association with delta beta-thalassemia. |
1983-12-20 |
2023-08-12 |
Not clear |
| T Harano, K Harano, S Shibata, S Ueda, H Mori, K Ima. Hb Chesapeake [alpha 92 (FG 4) Arg replaced by Leu] and Hb J Cape Town [alpha 92 (FG 4) Arg leads to Gln] first discovered in Japanese. Hemoglobin. vol 7. issue 5. 1983-12-20. PMID:6629827. |
hb chesapeake [alpha 92 (fg 4) arg replaced by leu] and hb j cape town [alpha 92 (fg 4) arg leads to gln] first discovered in japanese. |
1983-12-20 |
2023-08-12 |
Not clear |
| S Cin, N Akar, A O Cavdar, A Arcasoy, S Dedeoglu, B Webber, H Lam, T H Huisma. Hb Summer Hill or alpha 2 beta 2(52)(D3)Asp replaced by His in a Turkish family from Cyprus. Hemoglobin. vol 7. issue 5. 1983-12-20. PMID:6629828. |
hb summer hill or alpha 2 beta 2(52)(d3)asp replaced by his in a turkish family from cyprus. |
1983-12-20 |
2023-08-12 |
Not clear |
| T Harano, K Harano, S Shibata, S Ueda, J Tsuchida, K Marumoto, Y Yakeishi, T Murakam. Hb St. Luke's [alpha 95 (G2) Pro replaced by Arg] in Japan. Hemoglobin. vol 7. issue 5. 1983-12-20. PMID:6629829. |
hb st. luke's [alpha 95 (g2) pro replaced by arg] in japan. |
1983-12-20 |
2023-08-12 |
Not clear |
| T Harano, K Harano, S Shibata, S Ueda, K Imai, A Tsuneshige, H Yamada, M Seki, H Fuku. Hemoglobin Kariya [alpha 40 (C5) Lys leads to Glu]: a new hemoglobin variant with an increased oxygen affinity. FEBS letters. vol 153. issue 2. 1983-11-23. PMID:6137414. |
a new abnormal hemoglobin, hb kariya [alpha 40 (c5) lys leads to glu], with an amino acid substitution at the alpha 1 beta 2 contact was discovered in a young japanese man. |
1983-11-23 |
2023-08-12 |
Not clear |
| W F Moo-Penn, R M Baine, D L Jue, M H Johnson, J E McGuffey, J M Benso. Hemoglobin Evanston: alpha 14(A12) Trp leads to Arg. A variant hemoglobin associated with alpha-thalassemia-2. Biochimica et biophysica acta. vol 747. issue 1-2. 1983-10-28. PMID:6882779. |
hb evanston (alpha 14 trp leads to arg) was detected on cellulose acetate at ph 8.4 as a band with an electrophoretic mobility similar to that of hb s. in addition, a band migrating cathodic to hb a2 suggested the presence of a variant hb a2 with a substitution in the alpha-chain, a fact that was later confirmed by structural analysis. |
1983-10-28 |
2023-08-12 |
Not clear |
| M E Headlee, M B Gardiner, A L Reese, T H Huisma. The distribution of fetal hemoglobin and the types of gamma chain in red cell fractions separated by gradient centrifugation from blood of patients with sickle cell anemia and other hemoglobinopathies. Biochemical medicine. vol 29. issue 3. 1983-10-08. PMID:6193788. |
although an increased synthesis of hb-f with g gamma chains was again observed after in vitro incubation of reticulocytes with [35s]methionine none of the isolated cell fractions contained a hb f with the alpha 2 g gamma 2 composition. |
1983-10-08 |
2023-08-12 |
Not clear |
| C G Mathew, J Rousseau, J S Rees, E H Harle. The molecular basis of alpha thalassaemia in a South African population. British journal of haematology. vol 55. issue 1. 1983-10-08. PMID:6309210. |
the interaction of these determinants with each other or with the normal chromosome (alpha alpha/) produced the phenotypes alpha thalassaemia silent carrier, alpha thalassaemia trait and hb h disease. |
1983-10-08 |
2023-08-12 |
Not clear |
| C G Mathew, J Rousseau, J S Rees, E H Harle. The molecular basis of alpha thalassaemia in a South African population. British journal of haematology. vol 55. issue 1. 1983-10-08. PMID:6309210. |
the predominance of the -alpha/haplotype (21 out of the 28 alpha thalassaemia determinants) over the - -/haplotype is consistent with the low incidence of hb h disease and the apparent absence of hb bart's hydrops fetalis in this population group. |
1983-10-08 |
2023-08-12 |
Not clear |