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Inclusion bodies: Not that bad… [PDF]
Frontiers in Microbiology, 2014 The formation of inclusion bodies constitute a frequent event during the production of heterologous proteins in bacterial hosts. Although the mechanisms leading to their formation are not completely understood, empirical data have been exploited trying ...
Ana eRamon +2 more
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Current Opinion in Rheumatology, 2002 Inclusion body myositis (IBM) is an inflammatory myopathy with distinctive clinicopathologic features. The etiology of IBM remains elusive. The immune-mediated basis for this disease has been challenged by evidence implicating a number of divergent etiologic factors.
Rabi, Tawil, Robert C, Griggs
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Neurologic Clinics, 2012 The idiopathic inflammatory myopathies (IIMs) are a heterogeneous group of rare disorders that share many similarities. In addition to sporadic inclusion body myositis (IBM), these include dermatomyositis, polymyositis, and autoimmune necrotizing myopathy. IBM is the most common IIM after age 50 years.
Mazen M, Dimachkie, Richard J, Barohn
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Current Opinion in Rheumatology, 2011 Sporadic inclusion body myositis (sIBM) is a poorly understood immune and degenerative disease of skeletal muscle. Here, current opinion of the nature of this disease is summarized.Recent findings for sIBM include further characterization of muscle involvement through magnetic resonance imaging, the role of muscle as a host for immune cells, progress ...
Ivanidze, Jana +5 more
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Histopathologic bodies: An insight
Journal of International Clinical Dental Research Organization, 2011 The histopathological analysis of the tissue includes a detailed study of cellular and nuclear structures and their altered presentation in a given pathology.
Meena Kulkarni +2 more
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Autopsy Case Reports, 2023 Inclusion body fibromatosis is a benign, often locally recurring myofibroblastic tumor with distinctive intracytoplasmic eosinophilic inclusions. In 1965, Reye1 was the first to document this entity through a series of 6 cases of digital fibrous tumors of childhood, where he observed intracytoplasmic inclusion bodies.
Elgiva Iangngap +4 more
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Malakoplakia of the Uterus: A Rare Cause of Postmenopausal Bleeding Mimicking Malignancy [PDF]
Journal of Clinical and Diagnostic Research, 2019 Malakoplakia is a rare chronic granulomatous disease. It was first reported in 1902 by Michaelis and Gutmann. It may involve any part of the body, most commonly affecting the urinary tract, mainly the urinary bladder.
Chinmoyee Sonowal +4 more
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Inclusion bodies: a new concept
Microbial Cell Factories, 2010 In the last decades, the understanding of inclusion body biology and consequently, of their properties and potential biotechnological applications have dramatically changed. Therefore, the development of new purification protocols aimed to preserve those
García-Fruitós Elena
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Journal of Medical Case Reports, 2022 Background Lafora disease is a rare genetic disorder involving glycogen metabolism disorder. It is inherited by autosomal recessive pattern presenting as a progressive myoclonus epilepsy and neurologic deterioration beginning in adolescence.
Naim Zeka +8 more
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Microbiology Spectrum, 2023 The autotransporter protein secretion system has been used previously to target the secretion of heterologous proteins to the bacterial cell surface and the extracellular milieu at the laboratory scale.
Irene Beriotto +12 more
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