| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| M A Cürük, A Kutlar, T H Huisma. Hb Shelby [alpha 2 beta 2(131)(H9)Gln----Lys]-beta zero-thalassemia [codon 15 (TGG----TGA)] identified by DNA sequencing. Hemoglobin. vol 16. issue 5. 1992-12-14. PMID:1428946. |
hb shelby [alpha 2 beta 2(131)(h9)gln----lys]-beta zero-thalassemia [codon 15 (tgg----tga)] identified by dna sequencing. |
1992-12-14 |
2023-08-11 |
Not clear |
| K Fujisawa, Y Hattori, Y Ohba, S And. Hb Yuda or alpha 130(H13)Ala----Asp; a new alpha chain variant with low oxygen affinity. Hemoglobin. vol 16. issue 5. 1992-12-14. PMID:1428950. |
hb yuda or alpha 130(h13)ala----asp; a new alpha chain variant with low oxygen affinity. |
1992-12-14 |
2023-08-11 |
Not clear |
| B B Webber, J B Wilson, L H Gu, T H Huisma. Hb Ethiopia or alpha 2(140)(HC2)Tyr----His beta 2. Hemoglobin. vol 16. issue 5. 1992-12-14. PMID:1428951. |
hb ethiopia or alpha 2(140)(hc2)tyr----his beta 2. |
1992-12-14 |
2023-08-11 |
Not clear |
| S G Condò, M Corda, M T Sanna, M G Pellegrini, M P Ruiz, M Castagnola, B Giardin. Molecular basis of low-temperature sensitivity in pig hemoglobins. European journal of biochemistry. vol 209. issue 2. 1992-12-03. PMID:1425681. |
here we report a detailed functional characterization of pig hb, which, interpreted on the basis of the amino acid sequence of the alpha and beta chains of the molecule, sheds some light on the molecular basis of the phenomenon. |
1992-12-03 |
2023-08-11 |
human |
| H Wajcman, J Kister, M Marden, A Lahary, M Monconduit, F Galactero. Hemoglobin Rouen (alpha-140 (HC2) Tyr-->His): alteration of the alpha-chain C-terminal region and moderate increase in oxygen affinity. Biochimica et biophysica acta. vol 1180. issue 1. 1992-11-19. PMID:1390944. |
hb rouen (alpha 140(hc2) tyr-->his) is a moderately high oxygen-affinity variant that was found in coincidence with polycythemia vera in a french patient. |
1992-11-19 |
2023-08-11 |
Not clear |
| 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 |