Výsledky vyhledávání - "Elisavet Papapanagiotou"

A?-haplotypes: A new group of genetic markers for thalassemic mutations inside the 5? regulatory region of the human A?-globin gene

Autor: Aphrodite Loutradi-Anagnostou, Manoussos N. Papadakis, Dimitris Loukopoulos, Elisavet Papapanagiotou, George P. Patrinos, Panagoula Kollia

Publikováno v: American Journal of Hematology. 66:99-104

This study illustrates the relationship between a group of nucleotide variations within the 5' regulatory region of the Agamma-globin gene [Agamma-588 A-->G, Agamma-499 T-->A and the 4-bp deletion (Agamma-225 to -222 AGCA)] and the spectrum of delta-

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::670659ee161fb08ca35cb6f3e28f14ff
https://doi.org/10.1002/1096-8652(200102)66:2<99::aid-ajh1024>3.0.co

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Scanning method of identify the molecular heterogeneity of δ‐globin gene especially in δ‐thalassemias: Detection of three novel substitutions in the promoter region of the gene

Autor: Manoussos Papadakis, Elisavet Papapanagiotou, Afrodite Loutradi‐Anagnostou

Publikováno v: Human Mutation. 9:465-472

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::4fc6ae89dc05ddd66ea741b19b426a85
https://doi.org/10.1002/(sici)1098-1004(1997)9:5<465::aid-humu14>3.3.co

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Scanning method of identify the molecular heterogeneity of δ-globin gene especially in δ-thalassemias: Detection of three novel substitutions in the promoter region of the gene

Autor: Manoussos N. Papadakis, Afrodite Loutradi-Anagnostou, Elisavet Papapanagiotou

Publikováno v: Human Mutation. 9:465-472

A scanning strategy for the detection of δ-globin gene mutations and polymorphisms is presented. This procedure is based on the denaturing gradient gel electrophoresis (DGGE) of four different artificially amplified DNA fragments which cover the pro

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::54fafbfa52da8edb19fab51f4b53d81e
https://doi.org/10.1002/(sici)1098-1004(1997)9:5<465::aid-humu14>3.0.co

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δ-Thalassemic phenotype due to two 'novel' δ-globin gene mutations: CD11[GTC → GGC (A8)-HbA2-pylos] and CD 85 [TTT → TCT (F1)-HbA2-etolia]

Autor: Elisavet Papapanagiotou, Olga Drakoulakou, Manoussos N. Papadakis, Afrodite Loutradi-Anagnostou

Publikováno v: Human Mutation. 9:344-347

δ-Thalassemia reduces the expected HbA2 percentage, altering the normal as well as the β-thalassemia trait phenotype. An attempt to elucidate the molecular basis of δ-thalassemia in the Greek population, revealed two cases with unknown molecular d

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::5af3c9dacc7ba69d4448607c14cb3ed3
https://doi.org/10.1002/(sici)1098-1004(1997)9:4<344::aid-humu7>3.0.co

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