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Journal of the American Society of Brewing Chemists, ISSN 0361-0470, 04/2016, Volume 74, Issue 2, pp. 91 - 99
The haze-forming peptides and proteins present in beer mainly originate from the grains used. Such grains, typically barley and wheat, also incorporate gluten.... 
AN-PEP | Brewers Clarex | Gluten | Mass spectrometry | ELISA | An-pep | Brewers clarex | Elisa | ASPERGILLUS-NIGER | FOOD SCIENCE & TECHNOLOGY | T-CELL EPITOPES | MONOCLONAL-ANTIBODY | CELIAC-DISEASE PATIENTS | COMPETITIVE ELISA | CEREAL TOXICITY | GLIADIN PEPTIDES | HLA-DQ MOLECULES | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | PROLYL ENDOPROTEASE | TISSUE TRANSGLUTAMINASE
Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 04/2014, Volume 124, Issue 4, pp. 1821 - 1834
Journal Article
Molecular Therapy, ISSN 1525-0016, 02/2015, Volume 23, Issue 2, pp. 270 - 277
Journal Article
Journal Article
Molecular Immunology, ISSN 0161-5890, 2008, Volume 45, Issue 16, pp. 4138 - 4139
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 11/2011, Volume 20, Issue 22, pp. 4334 - 4344
Journal Article
Neuropathology and Applied Neurobiology, ISSN 0305-1846, 12/2014, Volume 40, Issue 7, pp. 873 - 887
Journal Article
Journal of Immunology, ISSN 0022-1767, 06/2008, Volume 180, Issue 11, pp. 7613 - 7621
Cells that undergo apoptosis or necrosis are promptly removed by phagocytes. Soluble opsonins such as complement can opsonize dying cells, thereby promoting... 
Journal Article
Alzheimer's & Dementia: The Journal of the Alzheimer's Association, ISSN 1552-5260, 2008, Volume 4, Issue 4, pp. T608 - T609
Journal Article
Genome Medicine, ISSN 1756-994X, 10/2013, Volume 5, Issue 10, pp. 95 - 95
Background: Spinal muscular atrophy (SMA) is a neuromuscular disease resulting from mutations in the survival motor neuron 1 (SMN1) gene. Recent breakthroughs... 
MOTOR-NEURONS | SMA | MORTALIN | MOUSE MODEL | GENETICS & HEREDITY | PHENOTYPE | DENERVATION | NEUROBLASTOMA | PATHOLOGY | STRESS | EXPRESSION | Proteins | Analysis | Proteomics | Muscles | Development and progression | Skin | Research | Biological markers | Atrophy, Muscular
Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 04/2014, Volume 124, Issue 4, pp. 1821 - 1821
The autosomal recessive neurodegenerative disease spinal muscular atrophy (SMA) results from low levels of survival motor neuron (SMN) protein; however, it is... 
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 06/2011, Volume 20, Issue 12, pp. 2406 - 2421
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 11/2010, Volume 19, Issue 21, pp. 4216 - 4228
Reduced expression of the survival motor neuron (SMN) gene causes the childhood motor neuron disease spinal muscular atrophy (SMA). Low levels of ubiquitously... 
Journal Article
2014
Low levels of survival motor neuron (SMN) protein cause the autosomal recessive neurodegenerative disease spinal muscular atrophy (SMA), through mechanisms... 
proteomics | disease mechanism | SMA | biomarkers | spinal muscular atrophy
Dissertation