PLoS ONE, ISSN 1932-6203, 12/2015, Volume 10, Issue 12, p. e0145783
Targeting protein stability with small molecules has emerged as an effective tool to control protein abundance in a fast, scalable and reversible manner. The...
CIRCUITS | LINKERS | STABILITY | MEMBRANE | MULTIDISCIPLINARY SCIENCES | PTEN | TUMOR-SUPPRESSOR | Gene Expression Regulation - drug effects | Protein Structure, Tertiary | Small Molecule Libraries - pharmacology | Animals | Gene Expression Regulation - genetics | Humans | Protein Stability - drug effects | Cell Line, Tumor | Zebrafish | Tacrolimus Binding Proteins - genetics | Proteins | Control systems | Neurosciences | Animal models | Cloning | Neurobiology | Biochemistry | Electrostatic properties | Kinases | Phosphatase | Control | Consolidation | Tacrolimus-binding protein | Penicillin | Cell cycle | Tagging | Tumor suppressor genes | Ligands | Control stability | PTEN protein | System effectiveness
CIRCUITS | LINKERS | STABILITY | MEMBRANE | MULTIDISCIPLINARY SCIENCES | PTEN | TUMOR-SUPPRESSOR | Gene Expression Regulation - drug effects | Protein Structure, Tertiary | Small Molecule Libraries - pharmacology | Animals | Gene Expression Regulation - genetics | Humans | Protein Stability - drug effects | Cell Line, Tumor | Zebrafish | Tacrolimus Binding Proteins - genetics | Proteins | Control systems | Neurosciences | Animal models | Cloning | Neurobiology | Biochemistry | Electrostatic properties | Kinases | Phosphatase | Control | Consolidation | Tacrolimus-binding protein | Penicillin | Cell cycle | Tagging | Tumor suppressor genes | Ligands | Control stability | PTEN protein | System effectiveness
Journal Article
Developmental Biology, ISSN 0012-1606, 2009, Volume 332, Issue 2, pp. 234 - 245
The chick spinal cord can regenerate following injury until advanced developmental stages. It is conceivable that changes in stem/progenitor cell plasticity...
Regeneration | Spinal cord | NeuN | Doublecortin | Glast | Injury | Development | Radial glia | Transitin | Chick | Neurogenesis | NEURAL PROGENITORS | INTERMEDIATE FILAMENT PROTEIN | DEVELOPMENTAL BIOLOGY | MICROTUBULE-ASSOCIATED PROTEIN | CNS STEM-CELLS | EMBRYONIC CHICK | CENTRAL-NERVOUS-SYSTEM | PRECURSOR CELLS | UP-REGULATION | EXPRESSION | Nestin | Microtubule-Associated Proteins - genetics | Microtubule-Associated Proteins - metabolism | Nerve Regeneration - physiology | Neurons - cytology | Stem Cells - cytology | Neuroglia - cytology | Intermediate Filament Proteins - genetics | Neurons - physiology | Neuropeptides - genetics | Spinal Cord - cytology | Biomarkers - metabolism | Spinal Cord Injuries - metabolism | Cells, Cultured | ELAV Proteins - metabolism | Neuroglia - physiology | Neuropeptides - metabolism | Chick Embryo | Nerve Tissue Proteins - genetics | Nerve Tissue Proteins - metabolism | Animals | Neurogenesis - physiology | Spinal Cord - physiology | Stem Cells - physiology | ELAV Proteins - genetics | Intermediate Filament Proteins - metabolism | Spinal cord injuries
Regeneration | Spinal cord | NeuN | Doublecortin | Glast | Injury | Development | Radial glia | Transitin | Chick | Neurogenesis | NEURAL PROGENITORS | INTERMEDIATE FILAMENT PROTEIN | DEVELOPMENTAL BIOLOGY | MICROTUBULE-ASSOCIATED PROTEIN | CNS STEM-CELLS | EMBRYONIC CHICK | CENTRAL-NERVOUS-SYSTEM | PRECURSOR CELLS | UP-REGULATION | EXPRESSION | Nestin | Microtubule-Associated Proteins - genetics | Microtubule-Associated Proteins - metabolism | Nerve Regeneration - physiology | Neurons - cytology | Stem Cells - cytology | Neuroglia - cytology | Intermediate Filament Proteins - genetics | Neurons - physiology | Neuropeptides - genetics | Spinal Cord - cytology | Biomarkers - metabolism | Spinal Cord Injuries - metabolism | Cells, Cultured | ELAV Proteins - metabolism | Neuroglia - physiology | Neuropeptides - metabolism | Chick Embryo | Nerve Tissue Proteins - genetics | Nerve Tissue Proteins - metabolism | Animals | Neurogenesis - physiology | Spinal Cord - physiology | Stem Cells - physiology | ELAV Proteins - genetics | Intermediate Filament Proteins - metabolism | Spinal cord injuries
Journal Article
Developmental Biology, ISSN 0012-1606, 07/2011, Volume 355, Issue 2, pp. 205 - 214
Spinal cord regenerative ability is lost with development, but the mechanisms underlying this loss are still poorly understood. In chick embryos, effective...
Development | Regeneration | Spinal cord | Peptidyl arginine deiminase | Deimination/citrullination | Apoptosis | MOUSE-BRAIN | EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS | CITRULLINATED PROTEINS | PEPTIDYLARGININE DEIMINASE | DEVELOPMENTAL BIOLOGY | FUNCTIONAL REPAIR | CELL-DEATH | MULTIPLE-SCLEROSIS | SPINAL-CORD-INJURY | GENETIC INFLUENCES | ARGININE METHYLATION | Hydrolases - metabolism | Immunohistochemistry | In Situ Nick-End Labeling | Age Factors | Oligonucleotide Array Sequence Analysis | Spinal Cord Injuries - metabolism | Apoptosis - drug effects | Calcium - metabolism | Humans | Ornithine - pharmacology | Ornithine - analogs & derivatives | DNA Primers - genetics | RNA, Messenger - metabolism | Chick Embryo | Blotting, Western | Spinal Cord Regeneration - physiology | Animals | Mass Spectrometry | Spinal Cord Injuries - embryology | Spinal Cord Injuries - physiopathology | Apoptosis - physiology | Protein-Arginine Deiminases | Gene Expression Regulation, Developmental - physiology | Hydrolases - antagonists & inhibitors | Post-translational modification | Proteins | Gene expression | Analysis | Enzymes | Calcium | Spinal cord injury | Substantia alba | Cavitation | Arginine | Developmental stages | Protein-arginine deiminase | Post-translation | Chelating agents | citrulline | development | regeneration | citrullination | apoptosis | deimination | peptidyl arginine deiminase | spinal cord
Development | Regeneration | Spinal cord | Peptidyl arginine deiminase | Deimination/citrullination | Apoptosis | MOUSE-BRAIN | EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS | CITRULLINATED PROTEINS | PEPTIDYLARGININE DEIMINASE | DEVELOPMENTAL BIOLOGY | FUNCTIONAL REPAIR | CELL-DEATH | MULTIPLE-SCLEROSIS | SPINAL-CORD-INJURY | GENETIC INFLUENCES | ARGININE METHYLATION | Hydrolases - metabolism | Immunohistochemistry | In Situ Nick-End Labeling | Age Factors | Oligonucleotide Array Sequence Analysis | Spinal Cord Injuries - metabolism | Apoptosis - drug effects | Calcium - metabolism | Humans | Ornithine - pharmacology | Ornithine - analogs & derivatives | DNA Primers - genetics | RNA, Messenger - metabolism | Chick Embryo | Blotting, Western | Spinal Cord Regeneration - physiology | Animals | Mass Spectrometry | Spinal Cord Injuries - embryology | Spinal Cord Injuries - physiopathology | Apoptosis - physiology | Protein-Arginine Deiminases | Gene Expression Regulation, Developmental - physiology | Hydrolases - antagonists & inhibitors | Post-translational modification | Proteins | Gene expression | Analysis | Enzymes | Calcium | Spinal cord injury | Substantia alba | Cavitation | Arginine | Developmental stages | Protein-arginine deiminase | Post-translation | Chelating agents | citrulline | development | regeneration | citrullination | apoptosis | deimination | peptidyl arginine deiminase | spinal cord
Journal Article
Developmental Neurobiology, ISSN 1932-8451, 05/2010, Volume 70, Issue 6, pp. 456 - 471
It is becoming apparent that regulation at the protein level plays crucial roles in developmental and pathological processes. Therefore, we performed a...
Collapsin Response Mediator protein | development | spinal cord | proteomics | regeneration | Development | Regeneration | Spinal cord | Collapsin response mediator protein | Proteomics | SIGNALING PATHWAYS | DIFFERENTIAL EXPRESSION | RESPONSE MEDIATOR PROTEIN-2 | GROWTH-CONE COLLAPSE | OUTGROWTH INHIBITION | AXONAL REGENERATION | DEVELOPMENTAL BIOLOGY | FUNCTIONAL REPAIR | NEUROSCIENCES | NEURITE OUTGROWTH | EMBRYONIC CHICK | NEURONAL POLARITY | Avian Proteins - metabolism | Phosphorylation | Spinal Cord - metabolism | Spinal Cord Injuries - metabolism | Intercellular Signaling Peptides and Proteins - genetics | Spinal Cord Injuries - genetics | Nerve Regeneration | RNA, Messenger - metabolism | Stem Cells - metabolism | Chick Embryo | Nerve Tissue Proteins - genetics | Nerve Tissue Proteins - metabolism | Intercellular Signaling Peptides and Proteins - metabolism | Spinal Cord - embryology | Animals | Protein Isoforms - metabolism | Gene Expression Regulation, Developmental | Cell Division | Neurons - metabolism | Spinal Cord Injuries - embryology | In Vitro Techniques | Avian Proteins - genetics
Collapsin Response Mediator protein | development | spinal cord | proteomics | regeneration | Development | Regeneration | Spinal cord | Collapsin response mediator protein | Proteomics | SIGNALING PATHWAYS | DIFFERENTIAL EXPRESSION | RESPONSE MEDIATOR PROTEIN-2 | GROWTH-CONE COLLAPSE | OUTGROWTH INHIBITION | AXONAL REGENERATION | DEVELOPMENTAL BIOLOGY | FUNCTIONAL REPAIR | NEUROSCIENCES | NEURITE OUTGROWTH | EMBRYONIC CHICK | NEURONAL POLARITY | Avian Proteins - metabolism | Phosphorylation | Spinal Cord - metabolism | Spinal Cord Injuries - metabolism | Intercellular Signaling Peptides and Proteins - genetics | Spinal Cord Injuries - genetics | Nerve Regeneration | RNA, Messenger - metabolism | Stem Cells - metabolism | Chick Embryo | Nerve Tissue Proteins - genetics | Nerve Tissue Proteins - metabolism | Intercellular Signaling Peptides and Proteins - metabolism | Spinal Cord - embryology | Animals | Protein Isoforms - metabolism | Gene Expression Regulation, Developmental | Cell Division | Neurons - metabolism | Spinal Cord Injuries - embryology | In Vitro Techniques | Avian Proteins - genetics
Journal Article
Molecular and Cellular Neuroscience, ISSN 1044-7431, 2006, Volume 33, Issue 2, pp. 188 - 199
The homologue of the microtubule associated protein MAP1B is encoded by the locus. The deduced protein Futsch is about twice the size of MAP1B and shows high...
NEURONAL MIGRATION | GROWTH CONES | GENE | PERIPHERAL NERVOUS-SYSTEM | GLYCOGEN-SYNTHASE KINASE-3 | WINGLESS | AXON GUIDANCE | SHAGGY | CELL-DIFFERENTIATION | 1B PHOSPHORYLATION | NEUROSCIENCES
NEURONAL MIGRATION | GROWTH CONES | GENE | PERIPHERAL NERVOUS-SYSTEM | GLYCOGEN-SYNTHASE KINASE-3 | WINGLESS | AXON GUIDANCE | SHAGGY | CELL-DIFFERENTIATION | 1B PHOSPHORYLATION | NEUROSCIENCES
Journal Article
Molecular and cellular neurosciences, ISSN 1044-7431, 10/2006, Volume 33, Issue 2, p. 188
The Drosophila homologue of the microtubule associated protein MAP1B is encoded by the futsch locus. The deduced protein Futsch is about twice the size of...
Microtubule-Associated Proteins - chemistry | Antibody Specificity | Phosphorylation | Microtubule-Associated Proteins - genetics | Species Specificity | Microtubule-Associated Proteins - metabolism | Glycogen Synthase Kinase 3 beta | Nerve Growth Factors - metabolism | Drosophila Proteins - immunology | Glycogen Synthase Kinase 3 - immunology | Drosophila Proteins - metabolism | Microtubules - metabolism | Conserved Sequence | Protein Structure, Tertiary | Amino Acid Sequence | Glycogen Synthase Kinase 3 - chemistry | Animals, Genetically Modified | Drosophila | Nerve Growth Factors - chemistry | Nerve Growth Factors - immunology | Drosophila Proteins - chemistry | Epitopes | Glycogen Synthase Kinase 3 - metabolism | Mammals | Microtubule-Associated Proteins - immunology | Animals | Glycogen Synthase Kinase 3 - genetics | Nerve Growth Factors - genetics | Drosophila Proteins - genetics | Mutation | Neuromuscular Junction - physiology
Microtubule-Associated Proteins - chemistry | Antibody Specificity | Phosphorylation | Microtubule-Associated Proteins - genetics | Species Specificity | Microtubule-Associated Proteins - metabolism | Glycogen Synthase Kinase 3 beta | Nerve Growth Factors - metabolism | Drosophila Proteins - immunology | Glycogen Synthase Kinase 3 - immunology | Drosophila Proteins - metabolism | Microtubules - metabolism | Conserved Sequence | Protein Structure, Tertiary | Amino Acid Sequence | Glycogen Synthase Kinase 3 - chemistry | Animals, Genetically Modified | Drosophila | Nerve Growth Factors - chemistry | Nerve Growth Factors - immunology | Drosophila Proteins - chemistry | Epitopes | Glycogen Synthase Kinase 3 - metabolism | Mammals | Microtubule-Associated Proteins - immunology | Animals | Glycogen Synthase Kinase 3 - genetics | Nerve Growth Factors - genetics | Drosophila Proteins - genetics | Mutation | Neuromuscular Junction - physiology
Journal Article
Molecular and Cellular Neuroscience, ISSN 1044-7431, 10/2006, Volume 33, Issue 2, p. 188
The Drosophila homologue of the microtubule associated protein MAP1B is encoded by the futsch locus. The deduced protein Futsch is about twice the size of...
Synthesis | Casein | Glycogen | Analysis | Drosophila | Phosphotransferases
Synthesis | Casein | Glycogen | Analysis | Drosophila | Phosphotransferases
Journal Article
9.
Full Text
The generation of disease-specific cell lines and their use for developing drug therapies
01/2012, ISBN 9781617792250
Book Chapter
Genetics Research, ISSN 0016-6723, 6/2007, Volume 89, Issue 3, pp. 181 - 188
Journal Article
Proceedings of the 14th EAI International Conference on mobile and ubiquitous systems: computing, networking and services, 11/2017, pp. 156 - 165
In-depth understanding of student life is essential to proactively support students in their academic educations. However, there is no work that identifies and...
heterogeneous data sources | user behavior analysis | smartphone | mobile sensing | student life | activity recognition | Student life | Activity recognition | Mobile sensing | User behavior analysis | Smartphone | Heterogeneous data sources
heterogeneous data sources | user behavior analysis | smartphone | mobile sensing | student life | activity recognition | Student life | Activity recognition | Mobile sensing | User behavior analysis | Smartphone | Heterogeneous data sources
Conference Proceeding
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