| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| K Ishimori, I Morishima, K Imai, K Fushitani, G Miyazaki, D Shih, J Tame, J Pegnier, K Niga. NMR study of human mutant hemoglobins synthesized in Escherichia coli. Consequences of tyrosine alpha 42 substitutions. The Journal of biological chemistry. vol 264. issue 25. 1989-10-11. PMID:2670922. |
these observations indicate that the hydrogen bond formed between tyr alpha 42 and asp beta 99 is required to convert unliganded hb to the t-state. |
1989-10-11 |
2023-08-11 |
human |
| M Z Atassi, M Yoshioka, G S Bixle. T cells specific for alpha-beta interface regions of hemoglobin recognize the isolated subunit but not the tetramer and indicate presentation without processing. Proceedings of the National Academy of Sciences of the United States of America. vol 86. issue 17. 1989-10-06. PMID:2788890. |
three hemoglobin (hb) alpha-chain synthetic peptides, corresponding to areas that are situated either completely [alpha-(31-45)] or partially [alpha-(41-45) and alpha-(81-95)] within the interface between the alpha and beta subunits of hb, and a fourth peptide representing a completely exposed area in tetrameric hb were used as immunogens in sjl/j (h-2s) mice. |
1989-10-06 |
2023-08-11 |
mouse |
| M Feola, J Simoni, D Fishman, R Tran, P C Canizar. Biocompatibility of hemoglobin solutions. I. Reactions of vascular endothelial cells to pure and impure hemoglobins. Artificial organs. vol 13. issue 3. 1989-09-13. PMID:2669694. |
incubation with a nonpure hb solution (hb plus red blood cell membrane aminophospholipids; a-pls) caused cell injury with significant release of tissue factor, plus a reaction characterized by 97.5 +/- 12.5% increase in txb2 production accompanied by 25.3 +/- 3% reduction in 6-keto-pgf1 alpha. |
1989-09-13 |
2023-08-11 |
human |
| M Feola, J Simoni, D Fishman, R Tran, P C Canizar. Biocompatibility of hemoglobin solutions. I. Reactions of vascular endothelial cells to pure and impure hemoglobins. Artificial organs. vol 13. issue 3. 1989-09-13. PMID:2669694. |
a second nonpure hb [hb plus bacterial environmental endotoxin (e)] caused cell injury, the release of tissue factor, and increased production of both prostaglandins, with greater release of txb2 (197 +/- 17%) than of 6-keto-pgf1 alpha (112 +/- 8.3%). |
1989-09-13 |
2023-08-11 |
human |
| W A Schroeder, D R Powars, L M Kay, L S Chan, V Huynh, J B Shelton, J R Shelto. Beta-cluster haplotypes, alpha-gene status, and hematological data from SS, SC, and S-beta-thalassemia patients in southern California. Hemoglobin. vol 13. issue 4. 1989-08-29. PMID:2473969. |
hb a2 levels increased with decrease in the number of alpha genes. |
1989-08-29 |
2023-08-11 |
Not clear |
| G Schiliro, C Rizzari, R Testa, F Lo Faro, F F Comisi, A Russ. Association of Hb S [beta 6(A3)Glu----Val] and Hb I-interlaken [alpha 15(A13)Gly----Asp] in a Sicilian man; review of the occurrence of Hb I-interlaken in Sicily. Hemoglobin. vol 13. issue 4. 1989-08-29. PMID:2666359. |
association of hb s [beta 6(a3)glu----val] and hb i-interlaken [alpha 15(a13)gly----asp] in a sicilian man; review of the occurrence of hb i-interlaken in sicily. |
1989-08-29 |
2023-08-11 |
Not clear |
| B Bohn, G Craescu, J Kister, J Bardakdjian, Y Blouquit, J Rosa, C Poyart, F Galactero. Structure-function of Hb Marseille-Long Island [alpha 2 beta 2 N-methionyl-2(NA2) His----Pro]. Hemoglobin. vol 13. issue 4. 1989-08-29. PMID:2753735. |
structure-function of hb marseille-long island [alpha 2 beta 2 n-methionyl-2(na2) his----pro]. |
1989-08-29 |
2023-08-11 |
Not clear |
| P F Como, T Wilkinson, H Kronenberg, J L Raven, J Prior, R J Tren. Hb Swan River [alpha 6(A4) Asp----Gly] initial identification in an Australian family. Hemoglobin. vol 13. issue 4. 1989-08-29. PMID:2753737. |
hb swan river [alpha 6(a4) asp----gly] initial identification in an australian family. |
1989-08-29 |
2023-08-11 |
Not clear |
| M C Martins, L Rosado, J B Wilson, A Kutlar, H Hu, T H Huisma. Hb Himeji or alpha 2 beta 2(140)(H18)Ala----Asp in a Portuguese family. Hemoglobin. vol 13. issue 4. 1989-08-29. PMID:2753739. |
hb himeji or alpha 2 beta 2(140)(h18)ala----asp in a portuguese family. |
1989-08-29 |
2023-08-11 |
Not clear |
| Y Ohba, K Imai, I Kumada, A Ohsawa, T Miyaj. Hb Moriguchi or alpha 2 beta 2(97) (FG4)His---Tyr substitution at the alpha 1-beta 2 interface. Hemoglobin. vol 13. issue 4. 1989-08-29. PMID:2775360. |
hb moriguchi or alpha 2 beta 2(97) (fg4)his---tyr substitution at the alpha 1-beta 2 interface. |
1989-08-29 |
2023-08-11 |
Not clear |
| C C Thompson, M A Ali, S Boyadjian, M Vacovsk. Positional effect of cis/trans alpha globin gene deletions on the formation of "H" bodies. American journal of hematology. vol 31. issue 4. 1989-08-04. PMID:2568088. |
however, patients with the two-gene deletion of the cis type alpha-thalassemia (alpha alpha/--) show the occasional "h" body, and those with hb "h" disease (alpha-/-- or alpha cs-/--) show many such bodies. |
1989-08-04 |
2023-08-11 |
human |
| H Wajcman, G Gombaud-Saintonge, F Galacteros, M Martha, F Vertonge. Hb Belliard [alpha 56(E5)Lys----Asn] a new fast-moving alpha chain variant found in a subject of Spanish origin. Hemoglobin. vol 13. issue 2. 1989-08-04. PMID:2737910. |
hb belliard [alpha 56(e5)lys----asn] a new fast-moving alpha chain variant found in a subject of spanish origin. |
1989-08-04 |
2023-08-11 |
human |
| J F Liu, Y Q Lu, X Q Liu, P Y Huang, C H Huang, S S Chen, P C Jia, C C Liang, C R Zu. Hb G-Taichung [alpha 74(EF3)Asp----His] in a Hunanese family in China. Hemoglobin. vol 13. issue 2. 1989-08-04. PMID:2737911. |
hb g-taichung [alpha 74(ef3)asp----his] in a hunanese family in china. |
1989-08-04 |
2023-08-11 |
Not clear |
| T Harano, K Harano, K Imai, H Yunoki, H Yagi, K Nagashima, T Kuroum. Hb J-Meerut [alpha 120(H3)Ala----Glu] found in a Japanese family. Hemoglobin. vol 13. issue 2. 1989-08-04. PMID:2737912. |
hb j-meerut [alpha 120(h3)ala----glu] found in a japanese family. |
1989-08-04 |
2023-08-11 |
Not clear |
| A R Bird, T Elliott, J B Wilson, B B Webber, H Hu, A Kutlar, F Kutlar, T H Huisma. Two rare unstable beta chain variants, Hb Mozhaisk or alpha 2 beta 292(F8)His----Arg and Hb Djelfa or alpha 2 beta 298(Fg5)Val----Ala, each being observed for the second time. Hemoglobin. vol 13. issue 2. 1989-08-04. PMID:2737917. |
two rare unstable beta chain variants, hb mozhaisk or alpha 2 beta 292(f8)his----arg and hb djelfa or alpha 2 beta 298(fg5)val----ala, each being observed for the second time. |
1989-08-04 |
2023-08-11 |
Not clear |
| K Imai, A Tsuneshige, T Harano, K Haran. Structure-function relationships in hemoglobin Kariya, Lys-40(C5) alpha----Glu, with high oxygen affinity. Functional role of the salt bridge between Lys-40 alpha and the beta chain COOH terminus. The Journal of biological chemistry. vol 264. issue 19. 1989-08-02. PMID:2500435. |
hb kariya, in which lys-40 alpha is replaced by glu, provides a unique opportunity to investigate the functional role of this salt bridge. |
1989-08-02 |
2023-08-11 |
Not clear |
| K Imai, A Tsuneshige, T Harano, K Haran. Structure-function relationships in hemoglobin Kariya, Lys-40(C5) alpha----Glu, with high oxygen affinity. Functional role of the salt bridge between Lys-40 alpha and the beta chain COOH terminus. The Journal of biological chemistry. vol 264. issue 19. 1989-08-02. PMID:2500435. |
these experimental results provide structural basis for explaining the oxygen binding characteristics of hb kariya and further give direct evidence that the intersubunit salt bridge between lys-40 alpha and the beta chain cooh terminus actually contributes to stabilization of the t quaternary structure, thereby playing a key role in cooperative oxygen binding by hemoglobin. |
1989-08-02 |
2023-08-11 |
Not clear |
| T P Molchanova, O A Mirgorodskaia, L V Abaturov, A V Podtelezhnikov, Iu N Tokare. [Location of amino acid substitutions in human hemoglobin. Mass spectrometric rapid analysis of tryptic peptides]. Molekuliarnaia biologiia. vol 23. issue 1. 1989-08-02. PMID:2739643. |
point mutations alpha 58 his----tyr (hb m boston), beta 6 glu--lys (hb c) and beta 26 glu----lys (hb e) have been identified in abnormal hemoglobins by means of tryptic hydrolysis of their alpha- and beta-chains followed by mass-spectrometry coupled with direct extraction of ions from solution. |
1989-08-02 |
2023-08-11 |
human |
| T P Molchanova, O A Mirgorodskaia, L V Abaturov, A V Podtelezhnikov, Iu N Tokare. [Location of amino acid substitutions in human hemoglobin. Mass spectrometric rapid analysis of tryptic peptides]. Molekuliarnaia biologiia. vol 23. issue 1. 1989-08-02. PMID:2739643. |
the abnormal hemoglobin hb m boston alpha 58 (e7) his----tyr has been for the first time found in the blood of a patient from the ussr. |
1989-08-02 |
2023-08-11 |
human |
| M Nagai, Y Yoneyama, T Kitagaw. Characteristics in tyrosine coordinations of four hemoglobins M probed by resonance Raman spectroscopy. Biochemistry. vol 28. issue 6. 1989-07-27. PMID:2730874. |
resonance raman spectra of four hemoglobins (hbs) m with tyrosinate ligand, that is, hb m saskatoon (beta distal his----tyr), hb m hyde park (beta proximal his----tyr), hb m boston (alpha distal his----tyr), and hb m iwate (alpha proximal his----tyr), were investigated in order to elucidate structural origins for distinctly facile reducibility of the abnormal subunit of hb m saskatoon in comparison with other hbs m. all of the hbs m exhibited the fingerprint bands for the fe-tyrosinate proteins around 1600, 1500, and 1270 cm-1. |
1989-07-27 |
2023-08-11 |
Not clear |