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Filamin-A susceptibility to calpain-mediated cleavage as a marker of dynamic conformational changes in intact platelets | bioRxiv
Identification of Filamin A Mechanobinding Partner II: Fimbacin Is a Novel Actin Cross-Linking and Filamin A Binding Protein | Biochemistry
Computational analysis of missense filamin-A variants, including the novel p.Arg484Gln variant of two brothers with periventricu
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FLNA mutations in surviving males presenting with connective tissue findings: two new case reports and review of the literature | BMC Medical Genetics | Full Text
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Filamin A (FLNA) is required for cell–cell contact in vascular development and cardiac morphogenesis | PNAS
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JCDD | Free Full-Text | MVP-Associated Filamin A Mutations Affect FlnA-PTPN12 (PTP-PEST) Interactions
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A) Schematic structure of FlnA. GPIbα, β3 and Syk bind to FlnA repeats... | Download Scientific Diagram
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Mutations in the Gene Encoding Filamin A as a Cause for Familial Cardiac Valvular Dystrophy | Circulation
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In-frame Variants in FLNA Proximal Rod 1 Domain Associate With a Predominant Cardiac Valvular Phenotype | Revista Española de Cardiología
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Terminal osseous dysplasia with pigmentary defects (TODPD) due to a recurrent filamin A (FLNA) mutation - Brunetti‐Pierri - 2014 - Molecular Genetics & Genomic Medicine - Wiley Online Library
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Current atomic structure of Filamin A (FLNA) cross-linking F-actin. (A)... | Download Scientific Diagram
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A Dual Phenotype of Periventricular Nodular Heterotopia and Frontometaphyseal Dysplasia in One Patient Caused by a Single FLNA Mutation Leading to Two Functionally Different Aberrant Transcripts - ScienceDirect
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Actin-binding protein filamin-A drives tau aggregation and contributes to progressive supranuclear palsy pathology | Science Advances
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The X‐linked filaminopathies: Synergistic insights from clinical and molecular analysis - Wade - 2020 - Human Mutation - Wiley Online Library
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Cytoskeletal protein filamin A is a nucleolar protein that suppresses ribosomal RNA gene transcription | PNAS
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