Matches in SemOpenAlex for { <https://semopenalex.org/work/W2164843676> ?p ?o ?g. }
- W2164843676 endingPage "1275" @default.
- W2164843676 startingPage "1259" @default.
- W2164843676 abstract "The sarcomere is the fundamental unit of cardiac and skeletal muscle contraction. During the last ten years, there has been growing awareness of the etiology of skeletal and cardiac muscle diseases originating in the sarcomere, an important evolving field. Many sarcomeric diseases affect newborn children, i. e. are congenital myopathies. The discovery and characterization of several myopathies caused by mutations in myosin heavy chain genes, coding for the major component of skeletal muscle thick filaments, has led to the introduction of a new entity in the field of neuromuscular disorders: myosin myopathies. Recently, mutations in genes coding for skeletal muscle thin filaments, associated with various clinical features, have been identified. These mutations evoke distinct structural changes within the sarcomeric thin filament. Current knowledge regarding contractile protein dysfunction as it relates to disease pathogenesis has failed to decipher the mechanistic links between mutations identified in sarcomeric proteins and skeletal myopathies, which will no doubt require an integrated physiological approach. The discovery of additional genes associated with myopathies and the elucidation of the molecular mechanisms of pathogenesis will lead to improved and more accurate diagnosis, including prenatally, and to enhanced potential for prognosis, genetic counseling and developing possible treatments for these diseases. The goal of this review is to present recent progress in the identification of gene mutations from each of the major structural components of the sarcomere, the thick and thin filaments, related to skeletal muscle disease. The genetics and clinical manifestations of these disorders will be discussed." @default.
- W2164843676 created "2016-06-24" @default.
- W2164843676 creator A5050841198 @default.
- W2164843676 date "2008-07-16" @default.
- W2164843676 modified "2023-09-25" @default.
- W2164843676 title "Thick and Thin Filament Gene Mutations in Striated Muscle Diseases" @default.
- W2164843676 cites W1481641418 @default.
- W2164843676 cites W1489998831 @default.
- W2164843676 cites W1520611067 @default.
- W2164843676 cites W1523872131 @default.
- W2164843676 cites W1581804688 @default.
- W2164843676 cites W1583696573 @default.
- W2164843676 cites W1588665322 @default.
- W2164843676 cites W1647386363 @default.
- W2164843676 cites W1901823973 @default.
- W2164843676 cites W1908481805 @default.
- W2164843676 cites W1964954465 @default.
- W2164843676 cites W1971782987 @default.
- W2164843676 cites W1971895613 @default.
- W2164843676 cites W1976374137 @default.
- W2164843676 cites W1976751662 @default.
- W2164843676 cites W1980323810 @default.
- W2164843676 cites W1982680252 @default.
- W2164843676 cites W1991194690 @default.
- W2164843676 cites W1994111603 @default.
- W2164843676 cites W1994817421 @default.
- W2164843676 cites W1997320938 @default.
- W2164843676 cites W1999251970 @default.
- W2164843676 cites W2001202329 @default.
- W2164843676 cites W2003254850 @default.
- W2164843676 cites W2004767153 @default.
- W2164843676 cites W2008801707 @default.
- W2164843676 cites W2009734614 @default.
- W2164843676 cites W2011513401 @default.
- W2164843676 cites W2019378998 @default.
- W2164843676 cites W2020890552 @default.
- W2164843676 cites W2024999459 @default.
- W2164843676 cites W2025590986 @default.
- W2164843676 cites W2025691770 @default.
- W2164843676 cites W2026182775 @default.
- W2164843676 cites W2026389814 @default.
- W2164843676 cites W2027142237 @default.
- W2164843676 cites W2028618453 @default.
- W2164843676 cites W2029578985 @default.
- W2164843676 cites W2029591319 @default.
- W2164843676 cites W2032278776 @default.
- W2164843676 cites W2033105576 @default.
- W2164843676 cites W2034005582 @default.
- W2164843676 cites W2038103542 @default.
- W2164843676 cites W2043239201 @default.
- W2164843676 cites W2044206268 @default.
- W2164843676 cites W2044629144 @default.
- W2164843676 cites W2055445948 @default.
- W2164843676 cites W2056736974 @default.
- W2164843676 cites W2060597743 @default.
- W2164843676 cites W2060912609 @default.
- W2164843676 cites W2062242528 @default.
- W2164843676 cites W2069953906 @default.
- W2164843676 cites W2070138631 @default.
- W2164843676 cites W2071737186 @default.
- W2164843676 cites W2071938993 @default.
- W2164843676 cites W2072255390 @default.
- W2164843676 cites W2073021990 @default.
- W2164843676 cites W2075785759 @default.
- W2164843676 cites W2076399493 @default.
- W2164843676 cites W2076579909 @default.
- W2164843676 cites W2081199349 @default.
- W2164843676 cites W2081390254 @default.
- W2164843676 cites W2087373820 @default.
- W2164843676 cites W2088879124 @default.
- W2164843676 cites W2091602849 @default.
- W2164843676 cites W2092436786 @default.
- W2164843676 cites W2092490000 @default.
- W2164843676 cites W2095417854 @default.
- W2164843676 cites W2101036829 @default.
- W2164843676 cites W2103801174 @default.
- W2164843676 cites W2105562470 @default.
- W2164843676 cites W2105685804 @default.
- W2164843676 cites W2105844750 @default.
- W2164843676 cites W2107575131 @default.
- W2164843676 cites W2111015914 @default.
- W2164843676 cites W2113172898 @default.
- W2164843676 cites W2113978444 @default.
- W2164843676 cites W2115576115 @default.
- W2164843676 cites W2121466366 @default.
- W2164843676 cites W2121951891 @default.
- W2164843676 cites W2126747143 @default.
- W2164843676 cites W2127423627 @default.
- W2164843676 cites W2138321124 @default.
- W2164843676 cites W2138475139 @default.
- W2164843676 cites W2141775696 @default.
- W2164843676 cites W2141873651 @default.
- W2164843676 cites W2146601153 @default.
- W2164843676 cites W2152315657 @default.
- W2164843676 cites W2166796432 @default.
- W2164843676 cites W2169287491 @default.
- W2164843676 cites W2315066195 @default.
- W2164843676 cites W2320122871 @default.