His primary areas of investigation include Cell biology, Molecular biology, Lamin, Muscular dystrophy and Nuclear protein. His studies deal with areas such as Immunology, Genetics and Cellular differentiation as well as Cell biology. His study looks at the intersection of Lamin and topics like Emerin with Emery–Dreifuss muscular dystrophy and Cell signaling.
Nadir M. Maraldi has researched Muscular dystrophy in several fields, including Myocyte and Collagen VI, Bethlem myopathy, Ullrich congenital muscular dystrophy. His Nuclear protein research is multidisciplinary, incorporating elements of Nuclear matrix, Cell nucleus, Internal medicine and Endocrinology. His work carried out in the field of Skeletal muscle brings together such families of science as Degeneration and Autophagy.
Nadir M. Maraldi mostly deals with Cell biology, Molecular biology, Lamin, Biochemistry and Chromatin. His Cell biology research includes themes of Genetics and Nuclear protein. His Molecular biology research incorporates elements of Collagen VI, Ullrich congenital muscular dystrophy, DNA, Phosphorylation and Phosphatidylinositol 4,5-bisphosphate.
In his study, Skeletal muscle is strongly linked to Pathology, which falls under the umbrella field of Collagen VI. His research integrates issues of Cellular differentiation, Transcription factor, Nuclear lamina and Emerin in his study of Lamin. His work carried out in the field of Chromatin brings together such families of science as Biophysics and Mandibuloacral dysplasia.
Nadir M. Maraldi mainly investigates Cell biology, Collagen VI, Lamin, Muscular dystrophy and Molecular biology. His Cell biology research is multidisciplinary, incorporating elements of Genetics, Nuclear protein, Emerin and Cellular differentiation. His Collagen VI research is mostly focused on the topic Ullrich congenital muscular dystrophy.
His research investigates the link between Ullrich congenital muscular dystrophy and topics such as Bethlem myopathy that cross with problems in Myopathy and Pathology. His Lamin study combines topics from a wide range of disciplines, such as Chromatin, Phenotype, Transcription factor and Nuclear lamina. His studies in Muscular dystrophy integrate themes in fields like Emery–Dreifuss muscular dystrophy, Cyclophilin and Anatomy.
Nadir M. Maraldi focuses on Cell biology, Lamin, Genetics, LMNA and Chromatin. His study in Cell biology is interdisciplinary in nature, drawing from both Multipotent Stem Cell and Cellular differentiation. As a part of the same scientific study, Nadir M. Maraldi usually deals with the Cellular differentiation, concentrating on Myogenesis and frequently concerns with Muscular dystrophy.
His Muscular dystrophy research focuses on Muscle strength and how it relates to Ullrich congenital muscular dystrophy and Collagen VI. The various areas that he examines in his Lamin study include Cell nucleus and Nuclear lamina. His research investigates the connection between LMNA and topics such as Nuclear protein that intersect with problems in Cell signaling, Nuclear matrix, Signal transduction and Progeroid syndromes.
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Autophagy is defective in collagen VI muscular dystrophies, and its reactivation rescues myofiber degeneration
Paolo Grumati;Luisa Coletto;Patrizia Sabatelli;Matilde Cescon.
Nature Medicine (2010)
Altered pre-lamin A processing is a common mechanism leading to lipodystrophy
Cristina Capanni;Elisabetta Mattioli;Marta Columbaro;Enrico Lucarelli.
Human Molecular Genetics (2005)
Cyclosporin A corrects mitochondrial dysfunction and muscle apoptosis in patients with collagen VI myopathies
Luciano Merlini;Alessia Angelin;Tania Tiepolo;Paola Braghetta.
Proceedings of the National Academy of Sciences of the United States of America (2008)
Regulation of novel protein kinase C ε by phosphorylation
Vittoria Cenni;Heike Döppler;Erica D. Sonnenburg;Nadir Maraldi.
Biochemical Journal (2002)
Mitochondrial dysfunction in the pathogenesis of Ullrich congenital muscular dystrophy and prospective therapy with cyclosporins
Alessia Angelin;Tania Tiepolo;Patrizia Sabatelli;Paolo Grumati.
Proceedings of the National Academy of Sciences of the United States of America (2007)
Rescue of heterochromatin organization in Hutchinson-Gilford progeria by drug treatment
M. Columbaro;C. Capanni;E. Mattioli;G. Novelli.
Cellular and Molecular Life Sciences (2005)
Ataxin-3 is Transported Into the Nucleus and Associates with the Nuclear Matrix
Danilo Tait;Massimo Riccio;Annie Sittler;Eberhard Scherzinger.
Human Molecular Genetics (1998)
Cellular and molecular events during chondrogenesis of human mesenchymal stromal cells grown in a three-dimensional hyaluronan based scaffold.
Gina Lisignoli;Sandra Cristino;Anna Piacentini;Stefania Toneguzzi.
Biomaterials (2005)
Heart-Specific Localization of Emerin: New Insights Into Emery-Dreifuss Muscular Dystrophy
Luca Cartegni;Marina Raffaele di Barletta;Rita Barresi;Stefano Squarzoni.
Human Molecular Genetics (1997)
Mutations in the retinoblastoma-related gene RB2/p130 in lung tumors and suppression of tumor growth in vivo by retrovirus-mediated gene transfer.
Pier Paolo Claudio;Candace M. Howard;Candace M. Howard;Carmen Pacilio;Carmen Pacilio;Caterina Cinti.
Cancer Research (2000)
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