Works matching DE "PROFILIN"


Results: 171
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    Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis.

    Published in:
    Nature, 2012, v. 488, n. 7412, p. 499, doi. 10.1038/nature11280
    By:
    • Wu, Chi-Hong;
    • Fallini, Claudia;
    • Ticozzi, Nicola;
    • Keagle, Pamela J.;
    • Sapp, Peter C.;
    • Piotrowska, Katarzyna;
    • Lowe, Patrick;
    • Koppers, Max;
    • McKenna-Yasek, Diane;
    • Baron, Desiree M.;
    • Kost, Jason E.;
    • Gonzalez-Perez, Paloma;
    • Fox, Andrew D.;
    • Adams, Jenni;
    • Taroni, Franco;
    • Tiloca, Cinzia;
    • Leclerc, Ashley Lyn;
    • Chafe, Shawn C.;
    • Mangroo, Dev;
    • Moore, Melissa J.
    Publication type:
    Article
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    Poster Presentations.

    Published in:
    Neuropathology & Applied Neurobiology, 2015, v. 41, p. 30, doi. 10.1111/nan.12224
    Publication type:
    Article
    28

    Influence of profilin on sensitisation profiles determined by cutaneous tests and IgE to major allergens in polysensitised patients.

    Published in:
    Clinical & Translational Allergy, 2016, v. 6, p. 1, doi. 10.1186/s13601-016-0114-y
    By:
    • Segura, Nieves;
    • Abos, Teresa;
    • Compaired, José A.;
    • Compés, Esther;
    • Guallar, Isabel;
    • Morales, Manuel;
    • Monzón, Susana;
    • Mozota, José;
    • Muñoz, Pilar;
    • Pola, Jesús;
    • Quintana, Macarena;
    • Rojas, Beatriz;
    • Juan, Sara San;
    • Villa, Felicitas;
    • Zapata, Cristina;
    • Jimeno, Lucía;
    • de la Torre, Fernando
    Publication type:
    Article
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    Sulfonylpiperazine compounds prevent Plasmodium falciparum invasion of red blood cells through interference with actin-1/profilin dynamics.

    Published in:
    PLoS Biology, 2023, v. 21, n. 4, p. 1, doi. 10.1371/journal.pbio.3002066
    By:
    • Dans, Madeline G.;
    • Piirainen, Henni;
    • Nguyen, William;
    • Khurana, Sachin;
    • Mehra, Somya;
    • Razook, Zahra;
    • Geoghegan, Niall D.;
    • Dawson, Aurelie T.;
    • Das, Sujaan;
    • Parkyn Schneider, Molly;
    • Jonsdottir, Thorey K.;
    • Gabriela, Mikha;
    • Gancheva, Maria R.;
    • Tonkin, Christopher J.;
    • Mollard, Vanessa;
    • Goodman, Christopher Dean;
    • McFadden, Geoffrey I.;
    • Wilson, Danny W.;
    • Rogers, Kelly L.;
    • Barry, Alyssa E.
    Publication type:
    Article
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    Profilin-1 mutations are rare in patients with amyotrophic lateral sclerosis and frontotemporal dementia.

    Published in:
    Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration, 2013, v. 14, n. 5/6, p. 463, doi. 10.3109/21678421.2013.787630
    By:
    • van Blitterswijk, Marka;
    • Baker, Matthew C.;
    • Bieniek, Kevin F.;
    • Knopman, David S.;
    • Josephs, Keith A.;
    • Boeve, Bradley;
    • Caselli, Richard;
    • Wszolek, Zbigniew K.;
    • Petersen, Ronald;
    • Graff-Radford, Neill R.;
    • Boylan, Kevin B.;
    • Dickson, Dennis W.;
    • Rademakers, Rosa
    Publication type:
    Article
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