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  • 1
    ISSN: 1432-0533
    Keywords: Electron microscopy ; Skeletal muscle ; Ring fibers (Ringbinden) ; Sarcoplasmic masses ; Sarcomere fragmentation ; Myofilaments
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Résumé Dans diverses conditions habituellement pathologiques, la fibre musculaire peut comporter une zone périphérique nettement individualisée et contenant des formations filamentaires dont la disposition spatiale est anormale. Les auteurs analysent les aspects ultrastructuraux de trois types de telles formations filamentaires périphériques: 1. lesfibrilles annulaires, bien visibles en microscopie optique; la microscopie électronique permet d'établir leur structure myofibrillaire normale, la fréquence des aspects complexes d'entretissage entre ces myofibrilles et les myofibrilles de disposition longitudinale; 2. lesmasses latérales dites “sarcoplasmiques” en microscopie optique, dont l'analyse en microscopie électronique permet d'établir la richesse fréquente en formations myofilamentaires disposées de façon anarchique; 3. lesempilements de fragments de sarcomère selon les différents plans de l'espace, qui ne peuvent être mis en évidence en microscopie optique, et n'apparaissent clairement qu'en microscopie électronique. L'étude ultrastructurale permet de récuser le caractère artificiel de ces différents aspects, souvent envisagé en microscopie optique, d'insister sur le caractère topographique limité le plus souvent à la périphérie de la fibre de telles altérations, et sur la fréquence de l'association de ces différentes anomalies entre elles. Cette étude apporte en outre des arguments en faveur de la nature dégénérative de ces aspects. Ces anomalies ne sont spécifiques d'aucune affection musculaire particulière, mais les auteurs les ont rencontrées cependant avec un maximum de fréquence dans les dystrophies musculaires progressives.
    Notes: Summary In various—usually pathologic—conditions the muscle fibre may show a distinct peripheral zone containing abnormally arranged filamentous formations. The authors have analysed the ultrastructural aspects of three types of such peripheral filamentous formations: 1.ring-shaped fibrils clearly visible under the light microscope; in these cases the electron microscope reveals their normal myofibrillar structure as well as the high incidence of complex formations resulting from the intertwining of such myofibrils and longitudinally disposed ones; 2. so-called“sarcoplasmic” lateral masses under light microscopy; in these cases the electron microscope shows a wealth of irregularly disposed myofilamentous formations; and 3.accumulations of sarcomere fragments at different spatial levels, which may be distinguished only under the electron microscope but not by light microscopy. The ultrastructural study permits the authors to disprove the artificial character of these different aspects—an assumption frequently made on the basis of light-microscopic findings—, to insist on the fact that such alterations are mostly limited topographically to the periphery of the fibre, and to stress that these different anomalies are often associated with one another. The study has furthermore furnished considerable evidence in favour of the degenerative nature of the forms under consideration. The anomalies in question are not specific to any one muscular affection; however they have been found most frequently in progressive muscular dystrophy.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Acta neuropathologica 13 (1969), S. 250-266 
    ISSN: 1432-0533
    Keywords: Electron Microscopy ; Congenital Myopathy ; Nemaline Myopathy ; Z-band Structure ; Sarcoplasmic Masses
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Résumé L'étude ultrastructurale d'une observation de «Nemaline-Myopathy» a été centrée sur les rapports structurels entre bâtonnets et stries Z normales dans différentes conditions de fixation. L'aspect des stries Z, en section transversale, varie en effet avec la fixation: réseau de ponts «obliques» (par rapport à l'alignement quadratique régulier des terminaisons des filaments fins) après fixation osmiée, réseau de ponts «transversaux», isolé ou superposé au premier réseau, après fixation aldéhydique initiale. L'aspect des bâtonnets en section transversale varie également avec la fixation; la disposition quadratique des filaments constitutifs des bâtonnets est visible après l'une et l'autre fixation, mais un réseau quadratique régulier, de 75 Å de côté, n'est clairement apparent qu'après fixation aldéhydique. Le point important est que ce dernier aspect diffère complètement du réseau «oblique» des stries Z normales, et peut être rapproché au contraire du réseau «transversal» de la strie Z obtenu après fixation aldéhydique; l'hypothèse est ainsi soulevée de la constitution des ponts dans les bâtonnets aux dépens d'un seul des deux constituants morphologiques de la strie Z. La topographie des bâtonnets a été également étudiée: tantôt périphérique, au sein de masses sarcoplasmiques latérales, tantôt centrale, au sein de petits foyers de désintégration myofibrillaire. La structure des plaques motrices visibles dans les préparations était normale. La spécificité de la lésion élémentaire et l'autonomie de ce type de myopathie sont ensuite discutées.
    Notes: Summary Ultrastructural study of an observation of “Nemaline Myopathy” has been focused on structural relationships between rods and normal Z-bands in different conditions of fixation. The Z-band structure studied in transversal section, varies with the fixation: network of “oblique” (relative to the regular quadratic pattern of the thin filament endings) bridges after osmic fixation; network of “transversal” bridges, alone or associated to the first network, after aldehydic fixation. The rod structure, in transversal section, is also varying with the fixation: a quadratic disposal of the filamentary content is visible after both fixations, but a regular quadratic network, 75–85 Å side, is clearly appearent only after aldehydic fixation. This last network differs from the “oblique” network of the normal Z-band; it can be compared to the “transversal” one obtained in the Z-band after aldehydic fixation. The hypothesis that bridges in the rods are formed only by one of the two normal morphological components of the Z-band, is raised. Topography of the rods in muscle fibers has been studied: either in peripheral sarcoplasmic masses, or in small central-located foci of myofibrillar disintegration. The end-plates structure was normal. Specificity of the elementary lesion, and autonomy of that type of myopathy is discussed.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Acta neuropathologica 6 (1966), S. 327-348 
    ISSN: 1432-0533
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-1203
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Desmin is a muscle-specific intermediate filament that is encoded by a gene assigned to human chromosome 2q35. Desmin-related myopathies are inherited disorders characterized by an intrasarcoplasmic accumulation of desmin. Recently, the knockout of the desmin gene was shown to generate a myopathic syndrome in transgenic mice, suggesting that functional abnormality of desmin may generate similar clinical symptoms in mouse and human. To determine the potential role of the desmin gene in a well-defined desmin-related myopathy (autosomal dominant form of Fardeau), human desmin cDNAs obtained from affected and unaffected individuals were cloned, sequenced and compared. No obvious mutation was detected. A BssHII restriction fragment length polymorphism (RFLP) was identified in exon 6 of the desmin gene. This RFLP was associated with a previously identified EcoRV RFLP in exon 4 to generate a tetra-allelic system, which was tested for linkage to the desmin-related myopathy in three families. The human desmin gene was localized within an 11-cM interval on chromosome 2q using a panel of radiation hybrids. This 11-cM region was clearly excluded by linkage analysis in the three desmin-related myopathy families using a set of highly polymorphic microsatellite markers. These results suggest that the desmin gene is not primarily involved in this disease.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1540-8159
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: BÉCANE, H.–M., et al.: High Incidence of Sudden Death with Conduction System and Myocardial Disease Due to Lamins A and C Gene Mutation. We studied 54 living relatives from a large French kindred, among which 17 members presented with a cardiomyopathy transmitted on an autosomal dominant mode. Five of these individuals had clinical manifestations of muscle disease phenotypically consistent with Emery-Dreifuss muscular dystrophy. Genetic analysis of this kindred had demonstrated a nonsense mutation in the LMNA gene located on chromosome 1q11–q23. This gene encodes lamins A and C, proteins of the nuclear lamina located on the inner face of the nuclear envelope. We retrospectively determined the cause of death of 15 deceased family members, 8 of whom had died suddenly, 2 as a first and single manifestation of the disease. The six other cases had histories of arrhythmias and left ventricular dysfunction before dying suddenly, and three of them died despite the prior implantation of a permanent pacemaker. The mean age of onset of cardiac symptoms among affected living family members was 33 years (range 15–47 years), and the first symptoms were due to marked atrioventricular conduction defects or sinus dysfunction, requiring the implantation of permanent pacemakers in seven cases. Myocardial dysfunction accompanied by ventricular arrhythmias developed rapidly in the course of the disease and resulted in severe dilated cardiomyopathy requiring cardiac transplantation in three cases. In conclusion, in patients presenting a life-threatening familial or sporadic cardiac restricted phenotype similar to that described here, mutations in the lamins A and C gene should be looked for. In the genotypically affected individuals, cardiological and electrophysiological follow-up should be performed to prevent sudden death that could occur rapidly in the evolution of such disease.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1546-1718
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Medicine
    Notes: [Auszug] Miyoshi myopathy (MM) is an adult onset, recessive inherited distal muscular dystrophy that we have mapped to human chromosome 2p13. We recently constructed a 3-Mb P1-derived artificial chromosome (PAC) contig spanning the MM candidate region. This clarified the order of genetic markers across ...
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1546-1718
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Medicine
    Notes: [Auszug] β–sarcoglycan, a 43 kDa dystrophin–associated glycoprotein, is an integral component of the dystrophin–glycoprotein complex. We have cloned human β–sarcoglycan cDNA and mapped the β–sarcoglycan gene to chromosome 4q12. Pericentromeric markers and an ...
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1432-1203
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The presence of nebulin in a muscle specimen from a patient with Duchenne muscular dystrophy (DMD) due to a large deletion precludes the possibility that this protein is the DMD gene product.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1546-170X
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Medicine
    Notes: [Auszug] Limb-girdle muscular dystrophy type 2A results from calpain 3 deficiency. In deltoid muscle biopsies of limb-girdle muscular dystrophy type 2A, myonuclear apoptosis was correlated here with altered subcellular distribution of IκBα and NF-κB, resulting in sarcoplasmic ...
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] FIG. 2 Immunohistochemical analysis of 50DAG in biopsied skeletal muscle using a monoclonal antibody against 50DAG (50DAG-1) and a sheep poly-clonal antibody affinity-purified against a 50DAG peptide (50DAG-2). Shown are (from top to bottom): 16-year-old male with no pathological changes in the ...
    Type of Medium: Electronic Resource
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