Search Results - "HATHOUT, Yetrib"
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Approaches to the study of the cell secretome
Published in Expert review of proteomics (01-04-2007)“…The secretome, or secretomics, has recently emerged as a new term to describe the global study of proteins that are secreted by a cell, tissue or organism at…”
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Large-scale serum protein biomarker discovery in Duchenne muscular dystrophy
Published in Proceedings of the National Academy of Sciences - PNAS (09-06-2015)“…Significance Duchenne muscular dystrophy (DMD) is a rare and devastating muscle disease caused by mutations in the X-linked DMD gene (which encodes the…”
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Proteomic and Bioinformatic Analysis of Decellularized Pancreatic Extracellular Matrices
Published in Molecules (Basel, Switzerland) (01-11-2021)“…Tissue microenvironments are rich in signaling molecules. However, factors in the tissue matrix that can serve as tissue-specific cues for engineering…”
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Discovery of serum protein biomarkers in the mdx mouse model and cross-species comparison to Duchenne muscular dystrophy patients
Published in Human molecular genetics (15-12-2014)“…It is expected that serum protein biomarkers in Duchenne muscular dystrophy (DMD) will reflect disease pathogenesis, progression and aid future therapy…”
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Biomarker-focused multi-drug combination therapy and repurposing trial in mdx mice
Published in PloS one (22-02-2021)“…Duchenne muscular dystrophy is initiated by dystrophin deficiency, but downstream pathophysiological pathways such as membrane instability, NFĸB activation,…”
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miR‐184 regulates ezrin, LAMP‐1 expression, affects phagocytosis in human retinal pigment epithelium and is downregulated in age‐related macular degeneration
Published in The FEBS journal (01-12-2014)“…MicroRNA 184 (miR‐184) is known to play a key role in neurological development and apoptosis and is highly expressed in mouse brain, mouse corneal epithelium,…”
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Identification of novel substrates for the serine protease HTRA1 in the human RPE secretome
Published in Investigative ophthalmology & visual science (01-07-2010)“…PURPOSE. To define the role of the serine protease HTRA1 in age-related macular degeneration (AMD) by examining its expression level and identifying its…”
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Toxoplasma membrane inositol phospholipid binding protein TgREMIND is essential for secretory organelle function and host infection
Published in Cell reports (Cambridge) (23-01-2024)“…Apicomplexan parasites possess specialized secretory organelles called rhoptries, micronemes, and dense granules that play a vital role in host infection. In…”
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Creation and characterization of an immortalized canine myoblast cell line: Myok9
Published in Mammalian genome (01-04-2020)“…The availability of an in vitro canine cell line would reduce the need for dogs for primary in vitro cell culture and reduce overall cost in pre-clinical…”
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Myoblasts and macrophages are required for therapeutic morpholino antisense oligonucleotide delivery to dystrophic muscle
Published in Nature communications (16-10-2017)“…Exon skipping is a promising therapeutic strategy for Duchenne muscular dystrophy (DMD), employing morpholino antisense oligonucleotides (PMO-AO) to exclude…”
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Identification of Disease Specific Pathways Using in Vivo SILAC Proteomics in Dystrophin Deficient mdx Mouse
Published in Molecular & cellular proteomics (01-05-2013)“…Duchenne muscular dystrophy (DMD) is an X-linked neuromuscular disorder caused by a mutation in the dystrophin gene. DMD is characterized by progressive…”
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Title-molecular diagnostics of dystrophinopathies in Sri Lanka towards phenotype predictions: an insight from a South Asian resource limited setting
Published in European journal of medical research (09-01-2024)“…The phenotype of Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD) patients is determined by the type of DMD gene variation, its location,…”
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Dystrophin deficiency leads to disturbance of LAMP1-vesicle-associated protein secretion
Published in Cellular and molecular life sciences : CMLS (01-06-2013)“…Duchenne muscular dystrophy results from loss of the protein dystrophin, which links the intracellular cytoskeletal network with the extracellular matrix, but…”
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Serum pharmacodynamic biomarkers for chronic corticosteroid treatment of children
Published in Scientific reports (17-08-2016)“…Corticosteroids are extensively used in pediatrics, yet the burden of side effects is significant. Availability of a simple, fast and reliable biochemical read…”
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Use of Quantitative Membrane Proteomics Identifies a Novel Role of Mitochondria in Healing Injured Muscles
Published in The Journal of biological chemistry (31-08-2012)“…Skeletal muscles are proficient at healing from a variety of injuries. Healing occurs in two phases, early and late phase. Early phase involves healing the…”
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Discovery of potential urine-accessible metabolite biomarkers associated with muscle disease and corticosteroid response in the mdx mouse model for Duchenne
Published in PloS one (16-07-2019)“…Urine is increasingly being considered as a source of biomarker development in Duchenne Muscular Dystrophy (DMD), a severe, life-limiting disorder that affects…”
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Morpholino‐induced exon skipping stimulates cell‐mediated and humoral responses to dystrophin in mdx mice
Published in The Journal of pathology (01-07-2019)“…Exon skipping is a promising genetic therapeutic strategy for restoring dystrophin expression in the treatment of Duchenne muscular dystrophy (DMD). The…”
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Advances in the proteomic investigation of the cell secretome
Published in Expert review of proteomics (01-06-2012)“…Studies of the cell secretome have greatly increased in recent years owing to improvements in proteomic platforms, mass spectrometry instrumentation and to the…”
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Discovery of Metabolic Biomarkers for Duchenne Muscular Dystrophy within a Natural History Study
Published in PloS one (15-04-2016)“…Serum metabolite profiling in Duchenne muscular dystrophy (DMD) may enable discovery of valuable molecular markers for disease progression and treatment…”
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Clinical utility of serum biomarkers in Duchenne muscular dystrophy
Published in Clinical proteomics (05-04-2016)“…Assessments of disease progression and response to therapies in Duchenne muscular dystrophy (DMD) patients remain challenging. Current DMD patient assessments…”
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