Works matching IS 14739542 AND DT 2017 AND VI 11

Results: 34
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    Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients.

    Published in:
    Human Genomics, 2017, v. 11, p. 1, doi. 10.1186/s40246-017-0126-2
    By:
    • Mitropoulos, Konstantinos;
    • Papadima, Eleni Merkouri;
    • Xiromerisiou, Georgia;
    • Balasopoulou, Angeliki;
    • Charalampidou, Kyriaki;
    • Galani, Vasiliki;
    • Zafeiri, Krystallia-Vassiliki;
    • Dardiotis, Efthymios;
    • Ralli, Styliani;
    • Deretzi, Georgia;
    • John, Anne;
    • Kydonopoulou, Kyriaki;
    • Papadopoulou, Elpida;
    • di Pardo, Alba;
    • Akcimen, Fulya;
    • Loizedda, Annalisa;
    • Dobričić, Valerija;
    • Novaković, Ivana;
    • Kostić, Vladimir S.;
    • Mizzi, Clint
    Publication type:
    Article
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    Whole transcriptome analysis of human erythropoietic cells during ontogenesis suggests a role of VEGFA gene as modulator of fetal hemoglobin and pharmacogenomic biomarker of treatment response to hydroxyurea in β-type hemoglobinopathy patients.

    Published in:
    Human Genomics, 2017, v. 11, p. 1, doi. 10.1186/s40246-017-0120-8
    By:
    • Chondrou, Vasiliki;
    • Kolovos, Petros;
    • Sgourou, Argyro;
    • Kourakli, Alexandra;
    • Pavlidaki, Alexia;
    • Kastrinou, Vlasia;
    • John, Anne;
    • Symeonidis, Argiris;
    • Ali, Bassam R.;
    • Papachatzopoulou, Adamantia;
    • Katsila, Theodora;
    • Patrinos, George P.
    Publication type:
    Article
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