| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| 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 |
| 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 enhanced tetramer-to-dimer dissociation previously observed in hb hirose (trp-37 beta----ser) together with our observation of the effects of organic phosphate on the structure and function of hb phe-37 beta suggested that a large part of the abnormal properties of hb phe-37 beta observed for dilute solutions appears to result from partial dissociation into alpha beta dimers rather than direct destabilization of the t-quaternary structure in the deoxygenated state. |
1992-05-01 |
2023-08-11 |
human |
| Y J Fei, J C Liu, E L Walker, T H Huisma. A new gene deletion involving the alpha 2-, alpha 1-, and theta 1-globin genes in a black family with Hb H disease. American journal of hematology. vol 39. issue 4. 1992-04-28. PMID:1553958. |
a new gene deletion involving the alpha 2-, alpha 1-, and theta 1-globin genes in a black family with hb h disease. |
1992-04-28 |
2023-08-11 |
Not clear |
| T Zwerdling, S Williams, S A Nasr, D L Rucknage. Hb Port Huron [alpha 56 (E5)Lys----ARG]: a new alpha chain variant. Hemoglobin. vol 15. issue 5. 1992-04-28. PMID:1802882. |
hb port huron [alpha 56 (e5)lys----arg]: a new alpha chain variant. |
1992-04-28 |
2023-08-11 |
Not clear |
| K Adachi, E Rappaport, H S Eck, P Konitzer, J Kim, S Surre. Polymerization and solubility of recombinant hemoglobins alpha 2 beta 2 (6Val) (Hb S) and alpha 2 beta 2(6Leu) (Hb Leu). Hemoglobin. vol 15. issue 5. 1992-04-28. PMID:1802884. |
polymerization and solubility of recombinant hemoglobins alpha 2 beta 2 (6val) (hb s) and alpha 2 beta 2(6leu) (hb leu). |
1992-04-28 |
2023-08-11 |
Not clear |
| R B Gupta, R S Tiwary, P L Pande, F Kutlar, C Oner, R Oner, T H Huisma. Hemoglobinopathies among the Gond tribal groups of central India; interaction of alpha- and beta-thalassemia with beta chain variants. Hemoglobin. vol 15. issue 5. 1992-04-28. PMID:1802886. |
the simultaneous presence of an alpha-thal (-alpha/alpha alpha or -alpha/-alpha) greatly improved the clinical and hematological condition of the patients with hb s-beta(+)-thal (ivs-i-5; g----c). |
1992-04-28 |
2023-08-11 |
human |
| R B Gupta, R S Tiwary, P L Pande, F Kutlar, C Oner, R Oner, T H Huisma. Hemoglobinopathies among the Gond tribal groups of central India; interaction of alpha- and beta-thalassemia with beta chain variants. Hemoglobin. vol 15. issue 5. 1992-04-28. PMID:1802886. |
lower hb f levels were present in 10 ss patients with an alpha-thal-2 homozygosity (average 16% versus 23.5% for eight ss patients with alpha alpha/alpha alpha) suggesting a decreased formation of alpha gamma dimers in severe alpha chain deficiency. |
1992-04-28 |
2023-08-11 |
human |
| R C Misra, B Ram, B C Mohapatra, S N Das, S C Misr. High prevalence & heterogenicity of thalassaemias in Orissa. The Indian journal of medical research. vol 94. 1992-04-08. PMID:1794898. |
high incidence of alpha thalassaemias (estimated from detection of hb bart's from cord blood), hb constant spring (cs) and high a2 beta thalassaemia trait (estimated from normal adult subjects) were detected in 12.6, 15 and 8 per cent people of coastal orissa (with less than 5% tribal population) respectively. |
1992-04-08 |
2023-08-11 |
human |
| R C Misra, B Ram, B C Mohapatra, S N Das, S C Misr. High prevalence & heterogenicity of thalassaemias in Orissa. The Indian journal of medical research. vol 94. 1992-04-08. PMID:1794898. |
quantitation of hb bart's suggest that the alpha thalassaemia could be any of the genotypes such as, -alpha/alpha alpha, -alpha/-alpha, --/alpha alpha and alpha alpha/alpha alpha cs. |
1992-04-08 |
2023-08-11 |
human |
| H Wajcman, J Kister, C Vasseur, Y Blouquit, J C Trastour, D Cottenceau, F Galactero. Structure of the EF corner favors deamidation of asparaginyl residues in hemoglobin: the example of Hb La Roche-sur-Yon [beta 81 (EF5) Leu----His]. Biochimica et biophysica acta. vol 1138. issue 2. 1992-04-03. PMID:1540659. |
deamidation has already been reported for two other variants of the ef corner, hb providence [beta 82 (ef6) lys----asn] and hb j singapore [alpha 79 (ef8) ala----gly]. |
1992-04-03 |
2023-08-11 |
Not clear |
| N H Jiang, S Liang, X J Wen, R Liang, C Su, Z Tan. Hb Westmead: an alpha 2-globin gene mutation detected by polymerase chain reaction and Stu I cleavage. Hemoglobin. vol 15. issue 4. 1992-03-24. PMID:1686260. |
hb westmead: an alpha 2-globin gene mutation detected by polymerase chain reaction and stu i cleavage. |
1992-03-24 |
2023-08-11 |
Not clear |
| N H Jiang, S Liang, X J Wen, R Liang, C Su, Z Tan. Hb Westmead: an alpha 2-globin gene mutation detected by polymerase chain reaction and Stu I cleavage. Hemoglobin. vol 15. issue 4. 1992-03-24. PMID:1686260. |
hb westmead or alpha 2 122(h5)his----gln beta 2 is one of the most common hemoglobin variants in guangxi, a province in southern china. |
1992-03-24 |
2023-08-11 |
Not clear |
| J B Wilson, M Ramachandran, B B Webber, F Kutlar, L F Hazelwood, D Barnett, N V Hirschler, T H Huisma. Hb Cleveland or alpha 2 beta 2(93)(F9)Cys----Arg;121(GH4)Glu----Gln. Hemoglobin. vol 15. issue 4. 1992-03-24. PMID:1787096. |
hb cleveland or alpha 2 beta 2(93)(f9)cys----arg;121(gh4)glu----gln. |
1992-03-24 |
2023-08-11 |
Not clear |
| Y C Gu, L H Gu, J B Wilson, B Cepreganova, M Ramachandran, E L Walker, T H Huisman, P Potiton. Hb Westmead [alpha 122(H5)His----Gln], Hb E [beta 26(B8)Glu----Lys], and alpha-thalassemia-2 (3.7 Kb deletion) in a Laotian family. Hemoglobin. vol 15. issue 4. 1992-03-24. PMID:1787098. |
hb westmead [alpha 122(h5)his----gln], hb e [beta 26(b8)glu----lys], and alpha-thalassemia-2 (3.7 kb deletion) in a laotian family. |
1992-03-24 |
2023-08-11 |
Not clear |
| S O Brennan, I R Lowrey, M G Harris, R Rodwell, K Zarkos, T Wilkinson, J Yakas, H Kronenber. Hb J-Camaguey [alpha 141(HC3)Arg----Gly] associated with alpha-thalassemia-1 in an Australian family. Hemoglobin. vol 15. issue 4. 1992-03-24. PMID:1787099. |
hb j-camaguey [alpha 141(hc3)arg----gly] associated with alpha-thalassemia-1 in an australian family. |
1992-03-24 |
2023-08-11 |
Not clear |
| J W Smit, K Deggeller, R Y Tamminga, J B Wilson, B B Webber, T H Huisma. Hb Fukuyama or alpha 2 beta(2)77(EF1)His----Tyr observed in an Indonesian female. Hemoglobin. vol 15. issue 4. 1992-03-24. PMID:1787102. |
hb fukuyama or alpha 2 beta(2)77(ef1)his----tyr observed in an indonesian female. |
1992-03-24 |
2023-08-11 |
Not clear |