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10,748 Possible Causes for complex, location, muscle, myosin

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  • Distal Myopathy

    Immunohistochemical staining for slow and fast myosin showed co-expression of slow and fast myosin in some type I fibres, possibly indicating a switch to type II status.[ncbi.nlm.nih.gov] Abstract Mutations in the myosin heavy chain gene (MYH7) can cause several distinct phenotypes depending on the location of the mutation: hypertrophic cardiomyopathy (several[ncbi.nlm.nih.gov] Abstract Distal myopathies are a group of clinically and pathologically overlapping muscle diseases that are genetically complex and can represent a diagnostic challenge.[ncbi.nlm.nih.gov] Two muscle biopsies were performed.[ncbi.nlm.nih.gov]

  • Influenza

    This movement likely represents the transport of virus-containing endocytic vesicles inside the cell, either directed by myosin motors on actin filaments ( 7 ) or propelled[doi.org] The incidence of influenza A(H1N1)pdm09 was higher in Ras Tanura city compared to other locations in the Eastern Province.[ncbi.nlm.nih.gov] Each genomic RNA segment exists in the form of a ribonucleoprotein complex (RNP) in association with nucleoproteins and an RNA-dependent RNA polymerase in virions.[ncbi.nlm.nih.gov] Abstract Immune-mediated necrotizing myopathy is a very rare inflammatory disease affecting skeletal muscles.[ncbi.nlm.nih.gov]

  • Barth Syndrome

    Cardiac myosin light chain ( cmlc ) cDNA clone was from Dr T. Zhong (Vanderbilt University).[ahajournals.org] Annotations Manually Curated Increase the total number of rows showing on this page using the pull-down located below the table, or use the page scroll at the table's top[yeastgenome.org] Thus, A88E BTHS mutant tafazzin complexes are specifically and selectively much more transient than wt Taz1p complexes.[jcb.rupress.org] Muscle AMP deaminase was deficient (5 resp. 17%).[ncbi.nlm.nih.gov]

  • Hyaline Body Myopathy

    Abstract Myosin storage myopathy/hyaline body myopathy is a rare congenital myopathy, with less than 30 cases reported in the literature.[ncbi.nlm.nih.gov] This location is critical for the proper assembly of sarcomeric myosin rod filaments.[gu.se] You may also want to contact a university or tertiary medical center in your area, because these centers tend to see more complex cases and have the latest technology and[rarediseases.info.nih.gov] After all this was the site of muscle contraction.[books.google.com]

  • Myosin Storage Myopathy

    myosin.[ncbi.nlm.nih.gov] This location is critical for the proper assembly of sarcomeric myosin rod filaments.[ncbi.nlm.nih.gov] Just as pediatric neurology evolved as an identified specialty as the volume and complexity of data became too much for the general pediatician or the adult neurologist to[books.google.de] You may also want to contact a university or tertiary medical center in your area, because these centers tend to see more complex cases and have the latest technology and[rarediseases.info.nih.gov]

  • Hypertrophic Cardiomyopathy

    […] and integration of a proportion of the myosin into the thick filaments and that myosin that is not integrated normally may migrate anomalously ( 26 ).[doi.org] The patients' electrocardiogram was compared with the location of the greatest myocardial hypertrophy by cardiac magnetic resonance.[ncbi.nlm.nih.gov] In conclusion, the association between LMNA mutations and different phenotypes is complex and not fully understood, and can present with a broad spectrum of severity.[ncbi.nlm.nih.gov] In the normal heart, the muscle cells are regular and patterned. In HCM the cells of the heart muscle become irregular and disordered.[patient.info]

  • Pulmonary Lymphangioleiomyomatosis

    Virgilio J J Cadete, Jolanta Sawicka, Lane K Bekar and Grzegorz Sawicki , Combined subthreshold dose inhibition of myosin light chain phosphorylation and MMP‐2 activity provides[doi.org] These tumors are rarely located retroperitoneally, with only about 15 such cases reported.[ncbi.nlm.nih.gov] Imaging evaluation plays an important role in the assessment of patients with tuberous sclerosis complex.[panafrican-med-journal.com] Abstract Proliferation, migration, and differentiation of smooth muscle (SM)-like lymphangioleiomyomatosis (LAM) cells in the lungs are pathologic manifestations of pulmonary[ncbi.nlm.nih.gov]

  • Familial Hypertrophic Cardiomyopathy Typ 7

    Mutations in beta-myosin S2 that cause familial hypertrophic cardiomyopathy (FHC) abolish the interaction with the regulatory domain of myosin-binding protein-C.[revespcardiol.org] Hypertrophic cardiomyopathy: Types CMH 1 Cardiac β- myosin heavy chain (MYH7) ; Chromosome 14q11.2; Dominant MYH7 Genetics Mutation type: Point mutations; 70 described Mutation locations[neuromuscular.wustl.edu] Intraatrial Reentrant Tachycardia in Complete Transposition of the Great Arteries Without Femoral Venous Access 197 Ventricular Tachycardia Following Surgical Repair of Complex[books.google.com] Molecular pathology Caused by defects of TNNI3, which encodes type-3 troponin I protein, TnI-cardiac (exclusively expressed in heart muscle).[medical-dictionary.thefreedictionary.com]

  • Nemaline Myopathy Type 7

    […] with myosin of normal muscle.[neurology.org] In summary, all mutations identified to date are located in the segment M162–M185.[pnas.org] A new symptom-complex consisting of deafness, dwarfism, cleft palate, characteristic facies, and a generalized bone dysplasia. Am. J. Dis. Child., 113:214, 1967. ‎[books.google.ro] The book provides a comprehensive review of most peripheral nerve and muscle diseases, including specific techniques and locations for performing each test.[books.google.com]

  • Lymphangioleiomyomatosis

    A particular pattern of gene expression, including high expression of ezrin (EZR), myosin heavy chain 10, non-muscle (MYH10), and myosin light chain kinase (MYLK) and a greatly[ncbi.nlm.nih.gov] Two types of LAM cells are recognized: 1) small, spindle-shaped cells that are centrally located in the LAM nodules and are highly immunoreactive for matrix metalloproteinase[doi.org] […] approved by the Food and Drug Administration, forms a complex with FK binding protein 12 and inactivates the target of rapamycin complex 1, abrogating the signaling.[doi.org] […] metabolism Myocytes, Smooth Muscle/pathology Myocytes, Smooth Muscle/physiology* Pluripotent Stem Cells/metabolism Pluripotent Stem Cells/pathology Pluripotent Stem Cells[ncbi.nlm.nih.gov]