Hasil Pencarian - Zeineb Bakey

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  1. 1
    Cleavage of periostin by MMP9 protects mice from kidney cystic disease

    Cleavage of periostin by MMP9 protects mice from kidney cystic disease oleh Nabila Djaziri, Cindy Burel, Lilia Abbad, Zeineb Bakey, Rémi Piedagnel, Brigitte Lelongt

    Diterbitkan 2023-01-01
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  2. 2
    Cleavage of periostin by MMP9 protects mice from kidney cystic disease.

    Cleavage of periostin by MMP9 protects mice from kidney cystic disease. oleh Nabila Djaziri, Cindy Burel, Lilia Abbad, Zeineb Bakey, Rémi Piedagnel, Brigitte Lelongt

    Diterbitkan 2023-01-01
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  3. 3
    ANKS3 Co-Localises with ANKS6 in Mouse Renal Cilia and Is Associated with Vasopressin Signaling and Apoptosis In Vivo in Mice.

    ANKS3 Co-Localises with ANKS6 in Mouse Renal Cilia and Is Associated with Vasopressin Signaling and Apoptosis In Vivo in Mice. oleh Laure Delestré, Zeineb Bakey, Cécilia Prado, Sigrid Hoffmann, Marie-Thérèse Bihoreau, Brigitte Lelongt, Dominique Gauguier

    Diterbitkan 2015-01-01
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  4. 4
    A 57 kB Genomic Deletion Causing CTNS Loss of Function Contributes to the CTNS Mutational Spectrum in the Middle East

    A 57 kB Genomic Deletion Causing CTNS Loss of Function Contributes to the CTNS Mutational Spectrum in the Middle East oleh Maryam Najafi, Maryam Najafi, Dor Mohammad Kordi Tamandani, Anoush Azarfar, Zeineb Bakey, Zeineb Bakey, Farkhondeh Behjati, Dinu Antony, Dinu Antony, Isabel Schüle, Simin Sadeghi-Bojd, Ehsan Ghayoor Karimiani, Ehsan Ghayoor Karimiani, Miriam Schmidts, Miriam Schmidts

    Diterbitkan 2019-03-01
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  5. 5
    Mimicry and well known genetic friends: molecular diagnosis in an Iranian cohort of suspected Bartter syndrome and proposition of an algorithm for clinical differential diagnosis

    Mimicry and well known genetic friends: molecular diagnosis in an Iranian cohort of suspected Bartter syndrome and proposition of an algorithm for clinical differential diagnosis oleh Maryam Najafi, Dor Mohammad Kordi-Tamandani, Farkhondeh Behjati, Simin Sadeghi-Bojd, Zeineb Bakey, Ehsan Ghayoor Karimiani, Isabel Schüle, Anoush Azarfar, Miriam Schmidts

    Diterbitkan 2019-02-01
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  6. 6
    Spectrum of Genetic Variants in a Cohort of 37 Laterality Defect Cases

    Spectrum of Genetic Variants in a Cohort of 37 Laterality Defect Cases oleh Dinu Antony, Dinu Antony, Elif Gulec Yilmaz, Alper Gezdirici, Lennart Slagter, Zeineb Bakey, Zeineb Bakey, Helen Bornaun, Ibrahim Cansaran Tanidir, Tran Van Dinh, Han G. Brunner, Han G. Brunner, Peter Walentek, Peter Walentek, Sebastian J. Arnold, Sebastian J. Arnold, Rolf Backofen, Rolf Backofen, Miriam Schmidts, Miriam Schmidts, Miriam Schmidts

    Diterbitkan 2022-04-01
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  7. 7
    IFT74 variants cause skeletal ciliopathy and motile cilia defects in mice and humans.

    IFT74 variants cause skeletal ciliopathy and motile cilia defects in mice and humans. oleh Zeineb Bakey, Oscar A Cabrera, Julia Hoefele, Dinu Antony, Kaman Wu, Michael W Stuck, Dimitra Micha, Thibaut Eguether, Abigail O Smith, Nicole N van der Wel, Matias Wagner, Lara Strittmatter, Philip L Beales, Julie A Jonassen, Isabelle Thiffault, Maxime Cadieux-Dion, Laura Boyes, Saba Sharif, Beyhan Tüysüz, Desiree Dunstheimer, Hans W M Niessen, William Devine, Cecilia W Lo, Hannah M Mitchison, Miriam Schmidts, Gregory J Pazour

    Diterbitkan 2023-06-01
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