Výsledky vyhledávání - "M Carla, Sollaino"

Induction of therapeutic levels of HbF in genome‐edited primary β 0 39‐thalassaemia haematopoietic stem and progenitor cells

Autor: Jiaming Wang, M Franca Marongiu, Maura Mingoia, Laura Manunza, Isadora Asunis, M. Giuseppina Marini, Yuet Wai Kan, Yukio Nakamura, Annalisa Cabriolu, Paolo Moi, Cristian Antonio Caria, Francesco Cucca, Lin Ye, Ryo Kurita, M Carla Sollaino

Publikováno v: British Journal of Haematology. 192:395-404

Hereditary persistence of fetal haemoglobin (HPFH) is the major modifier of the clinical severity of β-thalassaemia. The homozygous mutation c.-196 C>T in the Aγ-globin (HBG1) promoter, which causes Sardinian δβ0 -thalassaemia, is able to complet

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::25570a076b4a3fd13c7ff90b74b570e4
https://doi.org/10.1111/bjh.17167

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Induction of therapeutic levels of HbF in genome-edited primary β

Autor: Maura, Mingoia, Cristian A, Caria, Lin, Ye, Isadora, Asunis, M Franca, Marongiu, Laura, Manunza, M Carla, Sollaino, Jiaming, Wang, Annalisa, Cabriolu, Ryo, Kurita, Yukio, Nakamura, Francesco, Cucca, Yuet W, Kan, M Giuseppina, Marini, Paolo, Moi

Publikováno v: British journal of haematologyReferences. 192(2)

Hereditary persistence of fetal haemoglobin (HPFH) is the major modifier of the clinical severity of β-thalassaemia. The homozygous mutation c.-196 CT in the Aγ-globin (HBG1) promoter, which causes Sardinian δβ

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::a8e4b16955645de8560b0a91220a72f2
https://pubmed.ncbi.nlm.nih.gov/33216968

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