Works matching AU Aziz, Aziz ur Rehman

Results: 34
    1
    2

    Effect of Propolis on PPP2R1A and Apoptosis in Cancer Cells.

    Published in:
    Biochemistry Research International, 2025, v. 2025, p. 1, doi. 10.1155/bri/5538068
    By:
    • Durmaz, Burak;
    • Oktay Çelebi, Latife Merve;
    • Çekin, Ayşe;
    • Ahadova, Ayshan;
    • Günel, Nur Selvi;
    • Yıldırım, Hatice Kalkan;
    • Özgönül, Ali Mert;
    • Yıldırım Sözmen, Eser;
    • Aziz, Aziz ur Rehman
    Publication type:
    Article
    3
    4
    5
    6
    7
    8
    9
    10
    11
    12
    13
    14
    15
    16
    17
    18
    19
    20

    A Novel Missense Variant in Ultrarare SLC35A1‐CDG Alters Cellular Glycosylation, Lipid, and Energy Metabolism Without Affecting CDG Serum Markers.

    Published in:
    Human Mutation, 2025, v. 2025, p. 1, doi. 10.1155/humu/6290620
    By:
    • Falkenstein, Kristina;
    • Hoeren, Lukas;
    • Kikul, Frauke;
    • Poschet, Gernot;
    • Lüchtenborg, Christian;
    • Brecht, Ines B.;
    • Falb, Ruth;
    • Gauck, Darja;
    • Haack, Tobias;
    • Hecker, Andreas;
    • Himmelreich, Nastassja;
    • Okun, Jürgen G.;
    • Brügger, Britta;
    • Thiel, Christian;
    • Aziz, Aziz ur Rehman.
    Publication type:
    Article
    21
    22

    Deletion Testing of the DEGS1 Gene Should Be Part of the Diagnostic Pipeline for Hypomyelinating Leukodystrophy (HLD18).

    Published in:
    Human Mutation, 2025, v. 2025, p. 1, doi. 10.1155/humu/3531508
    By:
    • Zanobio, Mariateresa;
    • Nardecchia, Francesca;
    • Cappuccio, Gerarda;
    • Onore, Maria Elena;
    • Di Letto, Pasquale;
    • Rahman, Sarah Iffat;
    • Terrone, Gaetano;
    • Ugga, Lorenzo;
    • De Giorgi, Agnese;
    • Cas, Michele Dei;
    • Trinchera, Marco;
    • Leuzzi, Vincenzo;
    • Piluso, Giulio;
    • Nigro, Vincenzo;
    • Brunetti-Pierri, Nicola;
    • Torella, Annalaura;
    • Aziz, Aziz ur Rehman
    Publication type:
    Article
    23
    24
    25

    High Occurrence of a Missense Variant (c.471C>A) in the FGF23 Gene Related to Hyperostosis–Hyperphosphatemia Syndrome With a Possible Founder Effect.

    Published in:
    Human Mutation, 2025, v. 2025, p. 1, doi. 10.1155/humu/6382674
    By:
    • Sedghi, Maryam;
    • Gharehdaghi, Elika Esmaeilzadeh;
    • Ziaee, Vahid;
    • Abbasi, Farzaneh;
    • Meybodi, Hamid Reza Aghaei;
    • Smiley, Elina;
    • Mehdizadeh, Mehrzad;
    • Raeeskarami, Seyyed Reza;
    • Aslani, Nahid;
    • Shiran, Sahar Naderi;
    • Vafadar, Mehdi;
    • Amoli, Mahsa M.;
    • Aziz, Aziz ur Rehman
    Publication type:
    Article
    26
    27
    28
    29
    30
    31
    32
    33
    34