| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| S Liang, Z Tang, C Su, Q Lung, R Liang, Y J Fei, F Kutlar, J B Wilson, B B Webber, H H. Hb Duan [alpha 75(EF4)Asp----Ala], Hb Westmead [alpha 122(H5)His----Gln], and alpha-thalassemia-2 (-4.2 Kb deletion) in a Chinese family. Hemoglobin. vol 12. issue 1. 1988-08-02. PMID:3384694. |
detailed data are presented concerning the relative amounts of hb a and two alpha chain variants (hb duan with alpha 75 asp----ala, and hb westmead with alpha 122 his----gln), and the occurrence of an alpha-thalassemia-2 heterozygosity in five members of a small chinese family. |
1988-08-02 |
2023-08-11 |
Not clear |
| A Mrad, Y Blouquit, C Lacombe, R Blibech, N Arous, J Bardakdjian, R Kastally, J Rosa, F Galactero. Hb Tunis [alpha 2 beta 2 124 (H2)Pro----Ser], a new beta chain variant identified by HPLC. Hemoglobin. vol 12. issue 1. 1988-08-02. PMID:3384695. |
hb tunis [alpha 2 beta 2 124 (h2)pro----ser], a new beta chain variant identified by hplc. |
1988-08-02 |
2023-08-11 |
Not clear |
| T Harano, K Harano, N Imai, S Ueda, M Sek. An electrophoretically silent hemoglobin variant, Hb Hekinan [alpha 27(B8)Glu----Asp] found in a Japanese. Hemoglobin. vol 12. issue 1. 1988-08-02. PMID:3384699. |
an electrophoretically silent hemoglobin variant, hb hekinan [alpha 27(b8)glu----asp] found in a japanese. |
1988-08-02 |
2023-08-11 |
Not clear |
| A Mrad, N Arous, R Kastally, R Blibech, J Rosa, F Galactero. First observation of Hb Montgomery [alpha 48(CD6)Leu----Arg] in Tunisia. Hemoglobin. vol 12. issue 1. 1988-08-02. PMID:3384700. |
first observation of hb montgomery [alpha 48(cd6)leu----arg] in tunisia. |
1988-08-02 |
2023-08-11 |
Not clear |
| F F Costa, M A Zago, M F Sonati, C Bottur. The association of Hb Stanleyville II with alpha thalassemia and Hb S. Nouvelle revue francaise d'hematologie. vol 29. issue 6. 1988-07-19. PMID:3452204. |
the association of hb stanleyville ii with alpha thalassemia and hb s. two unrelated families are described which include two heterozygotes for hb stanleyville ii, two compound heterozygotes for hb stanleyville ii and hb s, and one compound homozygote for the two abnormal hemoglobins. |
1988-07-19 |
2023-08-11 |
Not clear |
| K J Garner, J B Lingre. Structural organization of the beta-globin locus of B-haplotype sheep. Molecular biology and evolution. vol 5. issue 2. 1988-06-17. PMID:3367782. |
goats and some sheep synthesize a juvenile hemoglobin, hb c (alpha 2 beta c2), at birth and produce this hemoglobin exclusively during severe anemia. |
1988-06-17 |
2023-08-11 |
Not clear |
| R E Weber, R Lalthantluanga, G Braunitze. Functional characterization of fetal and adult yak hemoglobins: an oxygen binding cascade and its molecular basis. Archives of biochemistry and biophysics. vol 263. issue 1. 1988-06-17. PMID:3369864. |
arranged in order of decreasing oxygen affinity the hbs are f1 (alpha i2 gamma 2), f2 (alpha ii2 gamma 2), a1 (alpha ii2 beta ii2), and cow hb a. |
1988-06-17 |
2023-08-11 |
Not clear |
| S K Ballas, W Koche. Erythrocytes in Hb SC disease are microcytic and hyperchromic. American journal of hematology. vol 28. issue 1. 1988-06-10. PMID:3369434. |
we have used the new technicon h.1 hematology analyzer to determine the indices of erythrocytes obtained from 18 nonthalassemic (alpha alpha/alpha alpha genotype) adult patients with hb sc disease. |
1988-06-10 |
2023-08-11 |
Not clear |
| L D Kwiatkowski, R W Nobl. Contribution of arginine (HC3) 141 alpha to the Bohr effect of the fourth binding step in the reaction of ligand with human hemoglobin. Proteins. vol 2. issue 1. 1988-05-26. PMID:3447169. |
we have compared the ph dependencies of the rate constants for the dissociation and combination of the fourth carbon monoxide molecule, l4 and l'4, respectively, for native hemoglobin a (hba) and a control reconstituted hba, and des-(arg 141 alpha) hba, the hemoglobin molecule resulting from the enzymatic removal of the c-terminal arginine of the alpha-chain of human hb. |
1988-05-26 |
2023-08-11 |
human |
| Y Ohba, K Yamamoto, Y Hattori, R Kawata, T Miyaj. Hyperunstable hemoglobin Toyama [alpha 2 136(H19)Leu----Arg beta 2]: detection and identification by in vitro biosynthesis with radioactive amino acids. Hemoglobin. vol 11. issue 6. 1988-05-24. PMID:2833478. |
the hemoglobin consisting of the abnormal alpha and normal beta chains eluted between hb a2 and hb a0 in anion exchange high performance liquid chromatography. |
1988-05-24 |
2023-08-11 |
Not clear |
| J M de Pablos, A Kutlar, J B Wilson, B B Webber, H Hu, T H Huisma. Hb D-Granada or alpha 2 beta 2 22(B4)Glu----Val. Hemoglobin. vol 11. issue 6. 1988-05-24. PMID:3446652. |
hb d-granada or alpha 2 beta 2 22(b4)glu----val. |
1988-05-24 |
2023-08-11 |
Not clear |
| F Baklouti, A Francina, E Dorléac, V Baudin-Chich, G Gombaud-Saintonge, H Plauchu, H Wajcman, J Delaunay, J Gode. Asymptomatic association of hemoglobin Dunn (alpha 6[A4]Asp----Asn) and hemoglobin O-Arab (beta 121[GH4]Glu----Lys) in a Moroccan man. American journal of hematology. vol 27. issue 4. 1988-05-12. PMID:3354560. |
we report on the association of hb dunn (alpha 6[a4]asp----asn) and hb o-arab (beta 121 [gh4]glu----lys) in a healthy moroccan man. |
1988-05-12 |
2023-08-11 |
Not clear |
| I Hiebl, G Braunitzer, D Schneegans. The primary structures of the major and minor hemoglobin-components of adult Andean goose (Chloephaga melanoptera, Anatidae): the mutation Leu----Ser in position 55 of the beta-chains. Biological chemistry Hoppe-Seyler. vol 368. issue 12. 1988-04-22. PMID:3442599. |
since hb a consists of alpha a2 beta 2 and hb d consists of alpha d2 beta 2 the mutation occurring in blood of the andean goose affects both hemoglobins whereas in the case of the barheaded goose only hb a is affected. |
1988-04-22 |
2023-08-11 |
Not clear |
| M Dahmane-Arbane, Y Blouquit, N Arous, J Bardakdjian, M Benamani, J Riou, M Benabadji, J Rosa, F Galactero. [Hemoglobin Boumerdès alpha 2(37) (C2) Pro----Arg beta 2: a new variant of the alpha chain associated with hemoglobin S in an Algerian family]. Nouvelle revue francaise d'hematologie. vol 29. issue 5. 1988-04-01. PMID:3438164. |
we report the first case of hb boumerdes, an alpha chain variant alpha 2(37) (c2) pro----arg beta 2, in an algerian family. |
1988-04-01 |
2023-08-11 |
Not clear |
| M Dahmane-Arbane, Y Blouquit, N Arous, J Bardakdjian, M Benamani, J Riou, M Benabadji, J Rosa, F Galactero. [Hemoglobin Boumerdès alpha 2(37) (C2) Pro----Arg beta 2: a new variant of the alpha chain associated with hemoglobin S in an Algerian family]. Nouvelle revue francaise d'hematologie. vol 29. issue 5. 1988-04-01. PMID:3438164. |
the abnormal hybrid hb alpha 2boum. |
1988-04-01 |
2023-08-11 |
Not clear |
| V S Sharm. Kinetic studies on partially liganded species of carboxyhemoglobin: alpha 2 CO beta 2 and alpha 2 beta 2CO. The Journal of biological chemistry. vol 263. issue 5. 1988-03-23. PMID:3339010. |
the valency hybrids of hb a, alpha 2co beta 2+, and alpha 2+ beta 2co have been prepared by a new high pressure liquid chromatography method, and the kinetics of their co-combination and dissociation reactions have been studied by double mixing and microperoxidase methods. |
1988-03-23 |
2023-08-11 |
Not clear |
| A V Hill, S L Thein, B Mavo, D J Weatherall, J B Cleg. Non-deletion haemoglobin H disease in Papua New Guinea. Journal of medical genetics. vol 24. issue 12. 1988-03-22. PMID:2892939. |
analysis of dna from members of a melanesian family from papua new guinea with haemoglobin (hb) h disease revealed that all four alpha globin genes are intact in affected subjects. |
1988-03-22 |
2023-08-11 |
human |
| J M de Pablos, J B Wilson, A Kutlar, F Kutlar, B B Webber, T H Huisma. Hb F-Kingston or alpha 2G gamma 2(55)(D6)Met----Arg in a Spanish newborn. Hemoglobin. vol 11. issue 5. 1988-03-11. PMID:2448270. |
hb f-kingston or alpha 2g gamma 2(55)(d6)met----arg in a spanish newborn. |
1988-03-11 |
2023-08-11 |
Not clear |
| C R Guest, L J No. Photodissociation of CO and O2 from alpha and beta hemoglobin chains studied by using picosecond absorption spectroscopy. Biophysical journal. vol 52. issue 5. 1988-03-11. PMID:3427192. |
we attribute this result to differences between the tertiary protein structure of the alpha and beta forms of hb, both distal and proximal. |
1988-03-11 |
2023-08-11 |
Not clear |
| M D Rhoda, C Domenget, M Vidaud, J Bardakdjian-Michau, P Rouyer-Fessard, J Rosa, Y Beuzar. Mouse alpha chains inhibit polymerization of hemoglobin induced by human beta S or beta S Antilles chains. Biochimica et biophysica acta. vol 952. issue 2. 1988-03-07. PMID:3337825. |
a murine model of sickle cell disease was tested by studying the polymerization of hybrid hemoglobin tetramers between alpha mouse and human beta s or beta s antilles chains were prepared from hb s antilles, which was a new sickling hemoglobin inducing a sickle cell syndrome more severe than hb s. the hybrid molecules did not polymerize in solution, indicating that the mouse alpha chains inhibited fiber formation. |
1988-03-07 |
2023-08-11 |
mouse |