| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| J V Langdown, R J Davidson, D Williamso. A new alpha chain variant, Hb Turriff [alpha 99(G6)Lys----Glu]: the interference of abnormal hemoglobins in Hb A1c determination. Hemoglobin. vol 16. issue 1-2. 1992-08-25. PMID:1634357. |
this new hemoglobin variant, hb turriff [alpha 99(g6)lys----glu], is not associated with any hematological disturbance, and family investigations indicate that it has arisen as a de novo mutation. |
1992-08-25 |
2023-08-11 |
Not clear |
| T A Cunningham, F Baker, N L Kobrinsky, B Cepreganova, E Baysal, J B Wilson, T H Huisma. The unstable Hb Hammersmith or alpha 2 beta 2(42)(CD1)Phe----Ser observed in an Indian child; identification by HPLC and by sequence analysis of amplified DNA. Hemoglobin. vol 16. issue 1-2. 1992-08-25. PMID:1634359. |
the unstable hb hammersmith or alpha 2 beta 2(42)(cd1)phe----ser observed in an indian child; identification by hplc and by sequence analysis of amplified dna. |
1992-08-25 |
2023-08-11 |
Not clear |
| T A Cunningham, F Baker, N L Kobrinsky, B Cepreganova, E Baysal, J B Wilson, T H Huisma. The unstable Hb Hammersmith or alpha 2 beta 2(42)(CD1)Phe----Ser observed in an Indian child; identification by HPLC and by sequence analysis of amplified DNA. Hemoglobin. vol 16. issue 1-2. 1992-08-25. PMID:1634359. |
we have identified the unstable hemoglobin variant present in a chipewayan indian patient with severe hemolytic anemia as hb hammersmith or alpha 2 beta 2(42)(cd1)phe----ser. |
1992-08-25 |
2023-08-11 |
Not clear |
| X J Wen, S Liang, Q Jin, W X Li. The nondeletional types of Hb H disease in Guangxi. Hemoglobin. vol 16. issue 1-2. 1992-08-25. PMID:1634361. |
the average hemoglobin level of the nondeletional hb h/cs (--/alpha alpha) is 6.8 g/dl, which is lower than that of the deletional types (7.9 g/dl), while the levels of hb h and hb bart's were much higher in the patients with hb h/cs than in those with the deletional types. |
1992-08-25 |
2023-08-11 |
Not clear |
| 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. |
twenty-three patients with hb h disease carried the southeast asian (sea) alpha-thalassemia-1 deletion; 13 had the alpha cs alpha (constant spring) nondeletional alpha-thalassemia-2 determinant, while the deletional alpha-thalassemia-2 (-3.7 or -4.2 kb) was present in 10 subjects. |
1992-08-25 |
2023-08-11 |
human |
| 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 |