All Relations between hb and alpha

Publication Sentence Publish Date Extraction Date Species
E George, H J Li, Y J Fei, A L Reese, E Baysal, B Cepreganova, J B Wilson, L H Gu, J F Nechtman, T A Stomin. Types of thalassemia among patients attending a large university clinic in Kuala Lumpur, Malaysia. Hemoglobin. vol 16. issue 1-2. 1992-08-25. PMID:1634362. the --/alpha cs alpha condition appeared to be the most severe with higher hb h values. 1992-08-25 2023-08-11 human
M Orisaka, T Tajima, T Harano, K Harano, Y Kushida, K Ima. A new alpha chain variant, Hb Hanamaki or alpha 2(139)(HC1)Lys----Glu beta 2, found in a Japanese family. Hemoglobin. vol 16. issue 1-2. 1992-08-25. PMID:1634363. a new alpha chain variant, hb hanamaki or alpha 2(139)(hc1)lys----glu beta 2, found in a japanese family. 1992-08-25 2023-08-11 Not clear
Y Tagawa, S Fujinami, Y Kadota, T Nakagawa, T Seki, Y Shiozaki, K Inoue, T Harano, K Harano, S Ued. Hb Olomouc [alpha 2 beta 2(86)(F2)Ala----Asp] found in a Japanese family. Hemoglobin. vol 16. issue 1-2. 1992-08-25. PMID:1634364. hb olomouc [alpha 2 beta 2(86)(f2)ala----asp] found in a japanese family. 1992-08-25 2023-08-11 Not clear
B Cepreganova, J B Wilson, T H Huisman, H A Hum. Hb Nottingham or alpha 2 beta 2(98)(FG5)Val----Gly observed as a de novo mutation in a Canadian child. Hemoglobin. vol 16. issue 1-2. 1992-08-25. PMID:1634365. hb nottingham or alpha 2 beta 2(98)(fg5)val----gly observed as a de novo mutation in a canadian child. 1992-08-25 2023-08-11 Not clear
C M Tseng, W Mitzne. Antagonists of EDRF attenuate acetylcholine-induced vasodilation in isolated hamster lungs. Journal of applied physiology (Bethesda, Md. : 1985). vol 72. issue 6. 1992-08-19. PMID:1629068. treatment of hamster lungs with each of the three edrf blockers, noarg (30 microm), hb (10 microm), and mb (250 microm), augmented the pressor responses to angiotensin ii and pgf2 alpha. 1992-08-19 2023-08-11 Not clear
C Vasseur, Y Blouquit, J Kister, D Promé, J S Kavanaugh, P H Rogers, C Guillemin, A Arnone, F Galacteros, C Poyar. Hemoglobin Thionville. An alpha-chain variant with a substitution of a glutamate for valine at NA-1 and having an acetylated methionine NH2 terminus. The Journal of biological chemistry. vol 267. issue 18. 1992-08-06. PMID:1618774. the x-ray crystal structure of deoxy hb thionville shows that the glutamate side chain extends away from the alpha 1-alpha 2 interface, whereas the methionine side chain (which has two conformations) extends into the alpha 1-alpha 2 interface, physically displacing chloride and bezafibrate. 1992-08-06 2023-08-11 Not clear
M Astatke, W A McGee, L J Parkhurs. A flow procedure to determine oxygen binding isotherms for low affinity and easily oxidized hemoglobins. Comparative biochemistry and physiology. B, Comparative biochemistry. vol 101. issue 4. 1992-07-30. PMID:1611887. at 22 degrees c, the half-saturation oxygen activity (x) is 227 microm, and the hill number is 0.91, for carp hb (t state) implying significant differences in the o2 affinities of the alpha and beta chain hemes or, two different t states. 1992-07-30 2023-08-11 Not clear
M M Keeling, S J Bertolone, E Baysal, Y C Gu, B Cepreganova, J B Wilson, T H Huisma. Hb Mizuho or alpha 2 beta (2)68(E12)Leu----Pro in a Caucasian boy with high levels of Hb F; identification by sequencing of amplified DNA. Hemoglobin. vol 15. issue 6. 1992-06-22. PMID:1726094. hb mizuho or alpha 2 beta (2)68(e12)leu----pro in a caucasian boy with high levels of hb f; identification by sequencing of amplified dna. 1992-06-22 2023-08-11 Not clear
S Liang, X J Wen, W X Li. Detection of the Hb Quong Sze mutation in a Chinese family by selective amplification of the alpha 2-globin gene and restriction map analysis with Msp I. Hemoglobin. vol 15. issue 6. 1992-06-22. PMID:1726096. detection of the hb quong sze mutation in a chinese family by selective amplification of the alpha 2-globin gene and restriction map analysis with msp i. 1992-06-22 2023-08-11 Not clear
S Liang, X J Wen, W X Li. Detection of the Hb Quong Sze mutation in a Chinese family by selective amplification of the alpha 2-globin gene and restriction map analysis with Msp I. Hemoglobin. vol 15. issue 6. 1992-06-22. PMID:1726096. the polymerase chain reaction technique combined with restriction map analysis with msp i and hybridization with synthetic oligonucleotide probes has been used to identify hb quong sze [alpha 125(h8)leu----pro] in a chinese family in guangxi (quong sze), p. r. china. 1992-06-22 2023-08-11 Not clear
K Teng, M S M. Hb F-Xinjiang or alpha 2A gamma T(2)25(B7)Gly----Arg identified by reversed phase HPLC; second observation. Hemoglobin. vol 15. issue 6. 1992-06-22. PMID:1726097. hb f-xinjiang or alpha 2a gamma t(2)25(b7)gly----arg identified by reversed phase hplc; second observation. 1992-06-22 2023-08-11 Not clear
B Cepreganova, L H Gu, J B Wilson, T H Huisma. A second observation of Hb F-Lodz or alpha 2G gamma (2)44(CD3)Ser----Arg. Hemoglobin. vol 15. issue 6. 1992-06-22. PMID:1726098. a second observation of hb f-lodz or alpha 2g gamma (2)44(cd3)ser----arg. 1992-06-22 2023-08-11 Not clear
G P Tamagnini, M L Ribeiro, V Valente, M Ramachandran, J B Wilson, E Baysal, L H Gu, T H Huisma. Hb Coimbra or alpha 2 beta (2)99(G1)Asp----Glu, a newly discovered highoxygen affinity variant. Hemoglobin. vol 15. issue 6. 1992-06-22. PMID:1814856. hb coimbra or alpha 2 beta (2)99(g1)asp----glu, a newly discovered highoxygen affinity variant. 1992-06-22 2023-08-11 Not clear
G P Tamagnini, M L Ribeiro, V Valente, M Ramachandran, J B Wilson, E Baysal, L H Gu, T H Huisma. Hb Coimbra or alpha 2 beta (2)99(G1)Asp----Glu, a newly discovered highoxygen affinity variant. Hemoglobin. vol 15. issue 6. 1992-06-22. PMID:1814856. the altered functional properties of hb coimbra likely result from the inability to form a hydrogen bond between beta 99glu and alpha 42tyr; such a bond is formed in deoxy hb a between the normally occurring beta 99asp and alpha 42tyr. 1992-06-22 2023-08-11 Not clear
G T Yüregir, K Aksoy, M A Cürük, N Dikmen, Y J Fei, E Baysal, T H Huisma. Hb H disease in a Turkish family resulting from the interaction of a deletional alpha-thalassaemia-1 and a newly discovered poly A mutation. British journal of haematology. vol 80. issue 4. 1992-06-18. PMID:1581238. several members had additional beta-chain abnormalities (hb s, hb d-los angeles, beta-thalassaemia); the 11 persons with a hb s heterozygosity and various alpha-globin gene defects (-alpha/alpha alpha; alpha t alpha/alpha alpha, - -/alpha alpha, -alpha/-alpha and - -/alpha t alpha) showed a decrease in the level of hb s that was directly related to the severity of the alpha-chain deficiency. 1992-06-18 2023-08-11 human
Y J Fei, J C Liu, V B Jogessar, K R Westermeyer, R Bridgemohan, T H Huisma. Combinations of three different forms of alpha-thalassemia in a large Indian family from Durban, South Africa: hematological observations. Acta haematologica. vol 87. issue 1-2. 1992-06-18. PMID:1585766. the rare south african (sa) type of alpha-thalassemia-1, which is characterized by an approximately 23-kb deletion involving the psi zeta, psi alpha 2, psi alpha 1, alpha 2, alpha 1, and theta 1 genes, was present in 13 members [6 simple heterozygotes, 5 with hb h disease of the --(sa)/-alpha(-3.7 kb) type, and 2 with hb h disease of the --(sa)/-alpha(-4.2 kb) type]. 1992-06-18 2023-08-11 Not clear
R Powers, D S Garrett, C J March, E A Frieden, A M Gronenborn, G M Clor. 1H, 15N, 13C, and 13CO assignments of human interleukin-4 using three-dimensional double- and triple-resonance heteronuclear magnetic resonance spectroscopy. Biochemistry. vol 31. issue 17. 1992-05-28. PMID:1567880. specifically, co(i)-n(i + 1),nh(i + 1) correlations are observed in the hnco experiment, the c alpha h(i), c alpha (i)-n(i + 1) correlations in the hca(co)n experiment, the c alpha(i)-n(i + 1),nh(i + 1) correlations in the hnca and hn(co)ca experiments, the c alpha h(i)-n(i + 1),nh(i + 1) correlations in the h(ca)nh and hn(co)hb experiments, and the c beta h(i)-n(i + 1),nh(i + 1) correlations in the hn(co)hb experiments. 1992-05-28 2023-08-11 human
b' S P Dibenedetto, G Russo Mancuso, A Di Cataldo, G Schilir\\xc3\\xb. Non inherited hemoglobin anomalies. Haematologica. vol 76. issue 5. 1992-05-14. PMID:1725283.' they include increased fetal hemoglobin (alpha 2 gamma 2), variations in hemoglobin a2 concentration, the presence of hb h (beta 4), bart's hb (gamma 4), hb köelliker, glycosylated, carbamylated and acetylated hemoglobins. 1992-05-14 2023-08-11 Not clear
A M Mashurov, Kh Kh Tkhan', D Kh Lan\. [Comparative estimation of phylogenesis of Vietnam dairy cattle using the Serebrovskiĭ, Hedrick and Rogers methods]. TSitologiia i genetika. vol 25. issue 6. 1992-05-07. PMID:1805470. starch gel electrophoresis has been used to study polymorphism of proteins of blood (hb, tf, al) and milk (alpha s1-cn, beta-cn, beta-lg) in animals of the holstein-friesian (n = 140), leisindian (n = 32) breeds and their hybrids (f1, n = 34); f2, n = 37; f3, n = 31) reared in vietnam. 1992-05-07 2023-08-11 cattle
K Ishimori, K Imai, G Miyazaki, T Kitagawa, Y Wada, H Morimoto, I Morishim. Site-directed mutagenesis in hemoglobin: functional and structural role of inter- and intrasubunit hydrogen bonds as studied with 37 beta and 145 beta mutations. Biochemistry. vol 31. issue 12. 1992-05-01. PMID:1554710. the mutant hb phe-37 beta, in which trp-37 beta is replaced by phe to remove the intersubunit hydrogen bond between asp-94 alpha and trp-37 beta at the alpha 1-beta 2 interface in deoxy hb a, showed a markedly increased oxygen affinity and almost completely diminished bohr effect and cooperativity. 1992-05-01 2023-08-11 human