Works about FRAMESHIFT mutation

Results: 1170
    1
    2
    3

    Several groups of LysM-RLKs are involved in symbiotic signal perception and arbuscular mycorrhiza establishment.

    Published in:
    Nature Communications, 2025, v. 16, n. 1, p. 1, doi. 10.1038/s41467-025-60717-1
    By:
    • Ding, Yi;
    • Lesterps, Zélie;
    • Gasciolli, Virginie;
    • Fuchs, Anne-Laure;
    • Gaston, Mégane;
    • Medioni, Lauréna;
    • de-Regibus, Annélie;
    • Remblière, Céline;
    • Vicédo, Céline;
    • Bensmihen, Sandra;
    • Bono, Jean Jacques;
    • Cullimore, Julie;
    • Reyt, Guilhem;
    • Dalmais, Marion;
    • Saffray, Christine;
    • Mazeau, Solène;
    • Bendahmane, Abdelhafid;
    • Sibout, Richard;
    • Vandenbussche, Michiel;
    • Rouster, Jacques
    Publication type:
    Article
    4

    A heterozygous CEBPA mutation disrupting the bZIP domain in a RUNX1 and SRSF2 mutational background causes MDS disease progression.

    Published in:
    Nature Communications, 2025, v. 16, n. 1, p. 1, doi. 10.1038/s41467-025-60192-8
    By:
    • Almaghrabi, Ruba;
    • Alyahyawi, Yara;
    • Keane, Peter;
    • Mian, Syed A.;
    • Habel, Khadidja;
    • Atkinson, Amelia;
    • Ward, Carl;
    • Bayley, Rachel;
    • Sargas, Claudia;
    • Menendez, Pablo;
    • Murphy, George J.;
    • Sobahy, Turki;
    • Baghdadi, Mohammed A.;
    • Flemban, Arwa F.;
    • Kabrah, Saeed M.;
    • Torres-Ruiz, Raul;
    • Papapetrou, Eirini P.;
    • Akerman, Ildem;
    • Raghavan, Manoj;
    • Barragan, Eva
    Publication type:
    Article
    5
    6
    7
    8

    Identification of DAGLB variants in Japanese early-onset Parkinson's disease.

    Published in:
    Journal of Neural Transmission, 2025, v. 132, n. 7, p. 1023, doi. 10.1007/s00702-025-02926-y
    By:
    • Luo, Yue;
    • Funayama, Manabu;
    • Hatano, Taku;
    • Li, Yuanzhe;
    • Yoshino, Hiroyo;
    • Yamashita, Satoshi;
    • Mori, Akira;
    • Nakamura, Ryoichi;
    • Hashizume, Yoshio;
    • Yoshida, Mari;
    • Riku, Yuichi;
    • Kanzato, Naomi;
    • Hattori, Nobutaka
    Publication type:
    Article
    9
    10
    11
    12
    13
    14
    15
    16
    17
    18
    19
    20
    21
    22
    23
    24
    25
    26
    27
    28
    29
    30

    Whole-Exome Sequencing of Rare Site Endometriosis-Associated Cancer.

    Published in:
    Diseases, 2021, v. 9, n. 1, p. 14, doi. 10.3390/diseases9010014
    By:
    • Kurose, Sonomi;
    • Nakayama, Kentaro;
    • Razia, Sultana;
    • Ishikawa, Masako;
    • Ishibashi, Tomoka;
    • Yamashita, Hitomi;
    • Sato, Seiya;
    • Sakiyama, Asuka;
    • Yoshioka, Shinya;
    • Kobayashi, Misa;
    • Nakayama, Satoru;
    • Otuski, Yoshiro;
    • Ishikawa, Noriyoshi;
    • Kyo, Satoru;
    • Battino, Maurizio
    Publication type:
    Article
    31
    32
    33
    34
    35
    36
    37
    38
    39
    40
    41
    42
    43
    44
    45
    46
    47
    48
    49
    50