| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| J R Hess, V W MacDonald, R M Winslo. Dehydration and shock: an animal model of hemorrhage and resuscitation of battlefield injury. Biomaterials, artificial cells, and immobilization biotechnology : official journal of the International Society for Artificial Cells and Immobilization Biotechnology. vol 20. issue 2-4. 1992-11-18. PMID:1391470. |
in a pilot study, resuscitation was performed with either ringer's lactate, albumin, stroma-free hemoglobin, or cross-linked (alpha alpha hb) hemoglobin. |
1992-11-18 |
2023-08-11 |
Not clear |
| P E Keipert, C L Gomez, A Gonzales, V W Macdonald, R M Winslo. The role of the kidneys in the excretion of chemically modified hemoglobins. Biomaterials, artificial cells, and immobilization biotechnology : official journal of the International Society for Artificial Cells and Immobilization Biotechnology. vol 20. issue 2-4. 1992-11-18. PMID:1391505. |
hb solutions tested were: plphb (hb monovalently reacted with pyridoxal 5'-phosphate); hbxl (hb crosslinked beta-beta with 2-nor-2-formylpyridoxal 5'-phosphate, or with bis-pyridoxal tetraphosphate); alpha alpha hb (hb cross-linked between the alpha-chains using bis-3,5-dibromosalicyl fumarate); and polyhb (polymerized with glutaraldehyde or o-raffinose). |
1992-11-18 |
2023-08-11 |
rat |
| D J Abraham, R A Peascoe, R S Randad, J Panikke. X-ray diffraction study of di and tetra-ligated T-state hemoglobin from high salt crystals. Journal of molecular biology. vol 227. issue 2. 1992-10-29. PMID:1404365. |
rsr-56 binds at two symmetry-related hb central water cavity sites and each molecule has major interactions with three different subunit side-chains; one effector with arg141 alpha 2 hc3, lys99 alpha 1 g6 and asn108 beta 1 and the other with the symmetry related residues, arg141 alpha 1 lys99 alpha 2 and asn108 beta 2. |
1992-10-29 |
2023-08-11 |
Not clear |
| P Beris, M N Kitundu, E Baysal, C Oner, K D Lanclos, A J Dimovski, F Kutlar, T H Huisma. Black beta-thalassemia homozygotes with specific sequence variations in the 5' hypersensitive site-2 of the locus control region have high levels of fetal hemoglobin. American journal of hematology. vol 41. issue 2. 1992-10-26. PMID:1384315. |
additional studies on relatives of the proband and on 10 unrelated black beta-thal homozygotes with either the c----t mutation at -88 or the a----g mutation at -29, confirm the possible importance of the sequence differences in the 5'hs-2, and also suggest that at least two additional factors, namely a c----t mutation at position -158 of the g gamma promoter and a relative deficiency in alpha chain synthesis play a (perhaps less important) role in the increased hb f synthesis in these patients. |
1992-10-26 |
2023-08-11 |
Not clear |
| D K Bowden, M A Vickers, D R Higg. A PCR-based strategy to detect the common severe determinants of alpha thalassaemia. British journal of haematology. vol 81. issue 1. 1992-10-15. PMID:1520607. |
this strategy should be useful in the development of screening programmes to identify carriers of alpha thalassaemia (--/alpha alpha) and prenatal diagnosis of the hb bart's hydrops fetalis syndrome (--/--) for those populations in which this represents a major cause of perinatal death. |
1992-10-15 |
2023-08-11 |
Not clear |
| M Ramachandran, L H Gu, J B Wilson, M N Kitundu, A D Adekile, J C Liu, K M McKie, T H Huisma. A new variant, HB Muscat [alpha 2 beta (2)32(B14)Leu----Val] observed in association with HB S in an Arabian family. Hemoglobin. vol 16. issue 4. 1992-10-08. PMID:1517102. |
a new variant, hb muscat [alpha 2 beta (2)32(b14)leu----val] observed in association with hb s in an arabian family. |
1992-10-08 |
2023-08-11 |
Not clear |
| T P Molchanova, J B Wilson, L H Gu, F Guemira, S Fattoum, T H Huisma. Hb Bab-Saadoun or alpha 2 beta (2)48(CD7)Leu----Pro, a mildly unstable variant found in an Arabian boy from Tunisia. Hemoglobin. vol 16. issue 4. 1992-10-08. PMID:1517103. |
hb bab-saadoun or alpha 2 beta (2)48(cd7)leu----pro, a mildly unstable variant found in an arabian boy from tunisia. |
1992-10-08 |
2023-08-11 |
Not clear |
| E V De Marco, L Crescibene, A Pasqua, C Brancati, M Bria, A Qualtier. HB Prato [alpha 31(B12)Arg----Ser] in a Calabrian family. Hemoglobin. vol 16. issue 4. 1992-10-08. PMID:1517104. |
hb prato [alpha 31(b12)arg----ser] in a calabrian family. |
1992-10-08 |
2023-08-11 |
Not clear |
| S K Ballas, D Park, L Fernandez, T K Hine, D L Jue, M H Johnson, W F Moo-Pen. Erythrocytosis secondary to HB Bunbury [alpha 2 beta (2)94(FG1)Asp----Asn]. Hemoglobin. vol 16. issue 4. 1992-10-08. PMID:1517105. |
erythrocytosis secondary to hb bunbury [alpha 2 beta (2)94(fg1)asp----asn]. |
1992-10-08 |
2023-08-11 |
Not clear |
| H Wajcman, Y Blouquit, C Vasseur, A Le Querrec, M Laniece, C Melevendi, A Rasore, F Galactero. Two new human hemoglobin variants caused by unusual mutational events: Hb Zaïre contains a five residue repetition within the alpha-chain and Hb Duino has two residues substituted in the beta-chain. Human genetics. vol 89. issue 6. 1992-09-29. PMID:1511986. |
hb zaïre [alpha 116(gh4)-his-leu-pro-ala-glu-117 (gh5)] is the second example in which a short amino acid sequence is inserted within the alpha-chain. |
1992-09-29 |
2023-08-11 |
human |
| Y Mizushima, T Kashii, K Nakagawa, S Monno, S Yan. Effects of granulocyte colony-stimulating factor, interleukin-1 alpha, and interleukin-6 on prolonged myelosuppression induced by nimustine hydrochloride in rats. Journal of immunotherapy : official journal of the Society for Biological Therapy. vol 12. issue 2. 1992-09-22. PMID:1380297. |
treatment of these animals with g-csf and il-1 alpha significantly enhanced the recovery of hb value as well as wbc count. |
1992-09-22 |
2023-08-11 |
rat |
| M Shyamala, C R Kiefer, H Moscoso, F A Garve. A monoclonal antibody-linked immunoassay for hemoglobin H disease. Annals of hematology. vol 65. issue 1. 1992-09-10. PMID:1643159. |
the decreased expression of alpha chains thus results in a reduction of the levels of normal hbs a and a2 and accumulation of beta 4, causing hb h disease. |
1992-09-10 |
2023-08-11 |
human |
| H Miyashita, K Hashimoto, H Mohri, T Ohokubo, T Harano, K Harano, K Ima. Hb Kanagawa [alpha 40(C5)Lys----Met]: a new alpha chain variant with an increased oxygen affinity. Hemoglobin. vol 16. issue 1-2. 1992-08-25. PMID:1634355. |
hb kanagawa [alpha 40(c5)lys----met]: a new alpha chain variant with an increased oxygen affinity. |
1992-08-25 |
2023-08-11 |
Not clear |
| H Miyashita, K Hashimoto, H Mohri, T Ohokubo, T Harano, K Harano, K Ima. Hb Kanagawa [alpha 40(C5)Lys----Met]: a new alpha chain variant with an increased oxygen affinity. Hemoglobin. vol 16. issue 1-2. 1992-08-25. PMID:1634355. |
structure determination studies, including amino acid analysis of the abnormal peptide and dna sequencing of a partially cloned alpha-globin gene, demonstrated that it is a new hemoglobin variant which has been named hb kanagawa [alpha 40(c5)lys----met]. |
1992-08-25 |
2023-08-11 |
Not clear |
| 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. |
a new alpha chain variant, hb turriff [alpha 99(g6)lys----glu]: the interference of abnormal hemoglobins in hb a1c determination. |
1992-08-25 |
2023-08-11 |
Not clear |
| 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 |