| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| 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 |
| V S Sharm. Kinetic studies on partially liganded species of carboxyhemoglobin: (alpha 1CO-beta 1CO)alpha 2 beta 2 or (alpha 2CO beta 2CO)alpha 1 beta 1. The Journal of biological chemistry. vol 264. issue 18. 1989-07-18. PMID:2732240. |
kinetics of co combination with and dissociation from isomer iii, (alpha 1co beta 1co)alpha 2 beta 2 or alpha 1 beta 1 (alpha 2co beta 2co), and hb rothschild have been studied using the double mixing and microperoxidase methods. |
1989-07-18 |
2023-08-11 |
Not clear |
| M J Ainley, B Mathieson, M Saar. Comparison of microcolumn chromatography and laser densitometry of isoelectric focusing strip for the quantitation of Hb A2 and Hb S. Clinical and laboratory haematology. vol 10. issue 4. 1989-07-17. PMID:3250791. |
in addition, paired analyses of 30 specimens, 20 sickle cell trait and 10 with sickle cell trait combined with alpha thalassaemia, were quantitated for hb s. the two groups were also well separated by both procedures and hb s levels were similar (r = +0.94, p less than 0.001). |
1989-07-17 |
2023-08-11 |
Not clear |
| F Kutlar, J M Gonzalez-Redondo, A Kutlar, A Gurgey, C Altay, G D Efremov, K Kleman, T H Huisma. The levels of zeta, gamma, and delta chains in patients with Hb H disease. Human genetics. vol 82. issue 2. 1989-06-30. PMID:2566576. |
this gamma chain was primarily present as hb bart's (or gamma 4) and only about 15% was recovered as hb f or alpha 2 gamma 2. |
1989-06-30 |
2023-08-11 |
Not clear |
| F Kutlar, J M Gonzalez-Redondo, A Kutlar, A Gurgey, C Altay, G D Efremov, K Kleman, T H Huisma. The levels of zeta, gamma, and delta chains in patients with Hb H disease. Human genetics. vol 82. issue 2. 1989-06-30. PMID:2566576. |
the low levels of hb a2 and of hb f (relative to hb bart's) can be explained by a decreased affinity of alpha chains for delta and gamma chains as compared with beta chains in conditions of severe alpha chain deficiency. |
1989-06-30 |
2023-08-11 |
Not clear |
| A de Tissera, L Balakumar, A Seneviratne, P Wickremasingh. The alpha thalassaemic syndrome of Hb H disease in a Sri Lankan family. The Ceylon medical journal. vol 33. issue 4. 1989-06-30. PMID:3248322. |
the alpha thalassaemic syndrome of hb h disease in a sri lankan family. |
1989-06-30 |
2023-08-11 |
Not clear |