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dolichyl-phosphate-mannose-protein mannosyltransferase (26) 26
index medicus (16) 16
proteins (14) 14
glycosylation (13) 13
mannosyltransferases - genetics (12) 12
mutation (12) 12
humans (11) 11
genes (10) 10
genetics & heredity (10) 10
dystroglycan (9) 9
muscular dystrophy (9) 9
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mannose (4) 4
mannosylation (4) 4
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Journal Article
Current Genetics, ISSN 0172-8083, 2/2019, Volume 65, Issue 1, pp. 223 - 239
In fungi, O-mannosylation is one type of conserved protein modifications that add the carbohydrate residues to specific residues of target proteins by protein... 
Biochemistry, general | Microbiology | Turgor pressure | Magnaporthe oryzae | Cell wall integrity | Cell Biology | Life Sciences | Pathogenicity | Microbial Genetics and Genomics | Proteomics | Protein O -mannosylation | ROS | Plant Sciences | Protein O-mannosylation | CONIDIATION | CELL-WALL INTEGRITY | AFFECT GROWTH | MANNOSYLATION | PROTEIN | PENETRATION | MORPHOGENESIS | PMT FAMILY | FULL VIRULENCE | GENETICS & HEREDITY | RICE BLAST FUNGUS | Gene Expression Regulation, Fungal | Hyphae - growth & development | Hyphae - genetics | Reactive Oxygen Species - metabolism | Oryza - metabolism | Spores, Fungal - growth & development | Fungal Proteins - genetics | Mannosyltransferases - genetics | Hyphae - metabolism | Virulence - genetics | Gene Expression Regulation, Developmental | Spores, Fungal - metabolism | Gene Deletion | Oryza - microbiology | Magnaporthe - pathogenicity | Mannosyltransferases - metabolism | Genetic Pleiotropy - genetics | Magnaporthe - growth & development | Magnaporthe - genetics | Spores, Fungal - genetics | Fungal Proteins - metabolism | Physiological aspects | Fungi, Pathogenic | Genetic aspects | Research | Transferases | Pathogens | Carbohydrates | Dolichyl-phosphate-mannose-protein mannosyltransferase | Residues | Plants (botany) | Extracellular enzymes | Pathogenesis | Genes | Virulence | Septum | Defects | Proteins | Fungi | Clonal deletion | Host plants | Hyphae | Deletion
Journal Article
Journal Article
The Journal of Neuroscience, ISSN 0270-6474, 02/2018, Volume 38, Issue 7, p. 1850
Genetic defects in protein O-mannosyltransferase 1 (POMT1) and POMT2 underlie severe muscular dystrophies. POMT genes are evolutionarily conserved in metazoan... 
Dolichyl-phosphate-mannose-protein mannosyltransferase | Phenotypes | Neurons | Genes | Drosophila | Transgenic | Muscles | Embryos | Muscle contraction | Mutants | Defects | Posture | Proteins | Wiring | Handedness | Insects | Etiology | Neural networks | Chirality | Sensory neurons | Sensory feedback | Torsion
Journal Article
PLoS ONE, ISSN 1932-6203, 07/2015, Volume 10, Issue 7, p. e0129914
O-mannosylation, the addition of mannose to serine and threonine residues of secretory proteins, is a highly conserved post-translational modification found in... 
YEAST | MORPHOGENESIS | AFFECT GROWTH | PLASMINOGEN-ACTIVATOR | MULTIDISCIPLINARY SCIENCES | MANNOSYLTRANSFERASE FAMILY | CELL-SURFACE | GENE FAMILY | ENDOPLASMIC-RETICULUM | SACCHAROMYCES-CEREVISIAE | GLYCOSYLATION PATHWAY | Osmotic Pressure | Glycosylphosphatidylinositols - genetics | Protein Multimerization | Chitinases - metabolism | Aspartic Acid Endopeptidases - genetics | Mannosyltransferases - genetics | Pichia - enzymology | Chitinases - genetics | Cell Membrane - chemistry | Mannose - metabolism | Hygromycin B - pharmacology | Glycosylphosphatidylinositols - chemistry | Isoenzymes - metabolism | Gene Deletion | Caffeine - pharmacology | Mannosyltransferases - metabolism | Phosphorylation - drug effects | Pichia - chemistry | Isoenzymes - genetics | Glycosylation | Cell Wall - chemistry | Fungal Proteins - genetics | Cell Membrane - enzymology | Glycosylphosphatidylinositols - metabolism | Aspartic Acid Endopeptidases - metabolism | Cell Wall - metabolism | Pichia - genetics | Mitogen-Activated Protein Kinases - genetics | Protein Processing, Post-Translational | Fungal Proteins - metabolism | Mitogen-Activated Protein Kinases - metabolism | Proteins | Post-translational modification | Comparative analysis | Health aspects | Chitinase | Dolichyl-phosphate-mannose-protein mannosyltransferase | Salts | Phosphorylation | Complex formation | Yeast | Serine | Genes | Mannose | Gene deletion | Cell surface | Defects | Clonal deletion | Pmt gene | Hygromycin B | Post-translation | Deletion | Bacteria | Life sciences | Caffeine | Recombinant | Threonine | Cell walls | Glycoproteins | Hygromycin | Membrane proteins | Anchors | Antibiotics | Insects | Plasmids | Cell size | Mutation | Aberration | Endoplasmic reticulum
Journal Article
PLoS ONE, ISSN 1932-6203, 2010, Volume 5, Issue 7, p. e11557
Journal Article
PLOS ONE, ISSN 1932-6203, 02/2017, Volume 12, Issue 2, p. e0170517
Purpose Congenital muscular dystrophy (CMD) is a heterogeneous disease entity. The detailed clinical manifestation and causative gene for each subgroup of CMD... 
ALPHA-DYSTROGLYCAN | MUTATIONS CAUSE | MULTIDISCIPLINARY SCIENCES | COLLAGEN VI MYOPATHIES | MUSCLE | PHENOTYPE | WALKER-WARBURG SYNDROME | BETHLEM MYOPATHY | GLYCOSYLATION | SPECTRUM | DEFICIENCY | Immunohistochemistry | Vesicular Transport Proteins - metabolism | Humans | Collagen Type VI - metabolism | Infant | Male | Mannosyltransferases - genetics | Muscular Dystrophies - genetics | Collagen Type VI - genetics | Antigens, Neoplasm - metabolism | Adult | Female | Mannosyltransferases - metabolism | Muscular Dystrophies - diagnosis | Retrospective Studies | Child | Antigens, Neoplasm - genetics | Muscular Dystrophies - metabolism | Vesicular Transport Proteins - genetics | Genotype | Lamin Type A - metabolism | Laminin - genetics | Asian Continental Ancestry Group | Adolescent | Lamin Type A - genetics | Taiwan | High-Throughput Nucleotide Sequencing | Laminin - metabolism | Usage | Analysis | Genetic aspects | Nucleotide sequencing | Epidemiology | Muscular dystrophy | Risk factors | DNA sequencing | Dolichyl-phosphate-mannose-protein mannosyltransferase | Pediatrics | Populations | Intelligence | Disease | Genomics | Epilepsy | Staining | Genomes | Gene sequencing | Genetics | Neck | Heart diseases | Genotypes | Sarcolemma | Dystroglycan | Neuromuscular diseases | Congenital diseases | Cardiac muscle | Muscles | Histology | Inflammation | Patients | Medicine | Pathology | Neurology | Hospitals | Biopsy | Collagen | Diagnostic software | Infiltration | Diagnostic systems | Dystrophy | Mutation | Psychiatry | Histochemistry
Journal Article
Annals of Human Genetics, ISSN 0003-4800, 09/2019, Volume 83, Issue 5, pp. 331 - 347
Introduction Limb‐girdle muscular dystrophy (LGMD) is the fourth most common muscular dystrophy, with progressive proximal muscle weakness. However, a large... 
variant | LGMD | NGS | WES | sarcolglycanopathies | GENE | GENETICS & HEREDITY | Dolichyl-phosphate-mannose-protein mannosyltransferase | Muscular dystrophy | Dystrophy
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 10/2017, Volume 114, Issue 42, p. 11163
The cadherin (cdh) superfamily of adhesion molecules carry O-linked mannose (O-Man) glycans at highly conserved sites localized to specific β-strands of their... 
Dystroglycan | Enzymes | CRISPR | Dolichyl-phosphate-mannose-protein mannosyltransferase | Hepatocyte growth factor | Genes | Strands | Homology | Glycosylation | Mannose | Cadherin | Machinery | Eukaryotes | Polysaccharides | Protein synthesis | Protocadherin | Lissencephaly | Evolutionary conservation | Elongation
Journal Article
Journal Article