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Identification of a founder mutation in TPM3 in nemaline myopathy patients of Turkish origin | European Journal of Human Genetics
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An Actin Filament Population Defined by the Tropomyosin Tpm3.1 Regulates Glucose Uptake - Kee - 2015 - Traffic - Wiley Online Library
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IJMS | Free Full-Text | The Primary Causes of Muscle Dysfunction Associated with the Point Mutations in Tpm3.12; Conformational Analysis of Mutant Proteins as a Tool for Classification of Myopathies
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IJMS | Free Full-Text | Overexpression of Tropomyosin Isoform Tpm3.1 Does Not Alter Synaptic Function in Hippocampal Neurons
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Physical interaction of tropomyosin 3 and STIM1 regulates vascular smooth muscle contractility and contributes to hypertension - ScienceDirect
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KM12C and KM12SM cells harbor the TPM3-NTRK1 gene fusion. (A) Schematic... | Download Scientific Diagram
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Tropomyosin Tpm3.1 Is Required to Maintain the Structure and Function of the Axon Initial Segment - ScienceDirect
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Tropomyosin Tpm3.1 is required to maintain the structure and function of the axon initial segment | bioRxiv
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Tropomyosin Tpm3.1 Is Required to Maintain the Structure and Function of the Axon Initial Segment - ScienceDirect
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Cells | Free Full-Text | Deletion of the Actin-Associated Tropomyosin Tpm3 Leads to Reduced Cell Complexity in Cultured Hippocampal Neurons—New Insights into the Role of the C-Terminal Region of Tpm3.1
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Dominant mutations in TPM3 affect amino acids located within or close... | Download Scientific Diagram
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