| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| 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 |
| N Akar, A Arcasoy, Y At. Hb Strumica [alpha(2)112(G19)His----Arg beta 2] in a Turkish family. Hemoglobin. vol 15. issue 4. 1992-03-24. PMID:1787106. |
hb strumica [alpha(2)112(g19)his----arg beta 2] in a turkish family. |
1992-03-24 |
2023-08-11 |
Not clear |
| P H Jensen, P Ebbesen, J Glieman. Low alpha 2-macroglobulin-proteinase complex binding: a common but not exclusive characteristic of malignant cells. In vivo (Athens, Greece). vol 3. issue 1. 1992-03-09. PMID:2485139. |
125i-labelled alpha 2-macroglobulin complexed with trypsin bound to human cancer cell lines (htb 144, crl 1427, ccl 30, hb 8065, ccl 2, crl 1593) but to a lesser degree than to normal cells. |
1992-03-09 |
2023-08-11 |
human |
| A Di Luccia, L Iannibelli, P Ferranti, L Manca, B Masala, L Ferrar. Electrophoretic and chromatographic evidence for allelic polymorphisms in the river buffalo alpha-globin gene complex. Biochemical genetics. vol 29. issue 9-10. 1992-02-27. PMID:1772399. |
two alpha-chains (i alpha 1 and ii alpha 3), and hbs with similar mobilities (hb1 and hb3), were associated with the aa hb phenotype: two alpha-chains (i alpha 2 and ii alpha 4), and hbs with different mobilities (hb2 and hb4), were associated with the bb phenotype: two sets of doublet hbs were associated with the ab phenotype, thus suggesting allelic polymorphisms at the two alpha loci. |
1992-02-27 |
2023-08-11 |
Not clear |
| V S Sharma, D Bandyopadhyay, M Berjis, J Rifkind, G R Bos. Double-mixing kinetic studies of the reactions of monoliganded species of hemoglobin: alpha 2(CO)1 beta 2 and alpha 2 beta 2(CO)1. The Journal of biological chemistry. vol 266. issue 36. 1992-02-07. PMID:1761549. |
the monoliganded species were generated by hybridization between excess ferric hb and alpha co2 beta +2 or alpha +2 beta co2 prepared by high-pressure liquid chromatography (hplc). |
1992-02-07 |
2023-08-11 |
Not clear |
| R Lindeman, R Wallace, F Volpato, S P Hu, R J Tren. Utility of the polymerase chain reaction (PCR) for prenatal diagnosis of genetic disease. Pathology. vol 23. issue 2. 1992-01-15. PMID:1745568. |
gene amplification by the polymerase chain reaction (pcr) has been applied to prenatal diagnosis for alpha and beta thalassemias (1 and 5 cases respectively), hemoglobin (hb) lepore/beta thalassemia (1 case) and cystic fibrosis (14 cases). |
1992-01-15 |
2023-08-11 |
Not clear |