Zobrazeno 1 - 10 of 12 pro vyhledávání: '"J L, Grech"'
1
The linkage of Hb Valletta [alpha 2 beta 287(f3)Thr----Pro] and Hb F-Malta-I [alpha 2G gamma 2117(G19)His----Arg] in the Maltese population
Autor: F, Kutlar, A E, Felice, J L, Grech, W H, Bannister, A, Kutlar, J B, Wilson, B B, Webber, H Y, Hu, T H, Huisman
Publikováno v: Human genetics. 86(6)
We have identified a new stable abnormal hemoglobin called Hb Valletta, which is characterized by a Thr----Pro substitution at position 87 of the beta chain. This mutation was found to be linked to that of the gamma chain variant Hb F-Malta-I with a
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::9c72853f4f2a8a2d5c24a8b33445be1d
https://pubmed.ncbi.nlm.nih.gov/1709134
Zobrazit plný text záznamu
2
Detection and quantitation of the fetal hemoglobin variant Hb F-Malta-I in adults
Autor: Titus H.J. Huisman, A. Felice, Fred A. Garver, J. L. Grech, W. H. Bannister, G. Altay
Publikováno v: Biochemical Genetics. 15:915-923
A variant of fetal hemoglobin (Hb F-Malta-I) has been detected and quantitated in adult blood with a sensitive radioimmunoassay employing monospecific antisera. The concentration of Hb-F-Malta-I was 0.002-0.05%, with an average value of 0.011%. The r
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2aea7e5666571f86a171e69911b9318f
https://doi.org/10.1007/bf00483988
Zobrazit plný text záznamu
5
Non-synchronized suppression of postnatal activity in non-allelic genes which synthesize the Ggamma chain in human foetal haemoglobin
Autor: W. H. Bannister, Walter A. Schroeder, J. L. Grech, A. K. Brown, Ruth N. Wrightstone, Titus H.J. Huisman
Publikováno v: Nature: New biology. 244(133)
HUMAN foetal haemoglobin (Hb-F) of the newborn is a heterogeneous protein, with two types of γ chains differing minimally in position 136 which is occupied either by a glycyl residue or by an alanyl residue1. The phenomenon is worldwide and is not l
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b978254856807e8a51b5a1615c236f8d
https://pubmed.ncbi.nlm.nih.gov/4516146
Zobrazit plný text záznamu
7
Evidence for four nonallelic structural genes for the chain of human fetal hemoglobin
Autor: J. L. Grech, W. A. Schroeder, W. H. Bannister, Titus H.J. Huisman
Publikováno v: Biochemical genetics. 7(2)
An abnormal human fetal hemoglobin not only may be either aGγ- or anAγ-chain variant but also may be present in a different proportion of the total fetal hemoglobin.Gγ-Chain variants contribute either about one-fourth or one-eighth to the total pr
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::949a93b80d7ea9bed72eedadf3dbfc0c
https://pubmed.ncbi.nlm.nih.gov/5050916
Zobrazit plný text záznamu
9
Glucose-6-phosphate dehydrogenase deficiency in Maltese newborn infants
Autor: Maria Vicatou, J. L. Grech
Publikováno v: British journal of haematology. 25(2)
Summary. A survey was carried out to establish the incidence of erythrocyte glucose-6-phosphate dehydrogenase deficiency in newborn infants in the Maltese islands. Of the infants born during the period of the survey 28.7% were tested: 1147 samples we
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36cd8b7255458b7c8995ae6ba1d450d6
https://pubmed.ncbi.nlm.nih.gov/4726905
Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání

Omezení vyhledávání
Plný text Recenzováno Digitální knihovna AV ČR
Zdroje