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PLoS ONE, ISSN 1932-6203, 03/2013, Volume 8, Issue 3, pp. e58333 - e58333
Journal Article
Cancer Research, ISSN 0008-5472, 02/2005, Volume 65, Issue 3, pp. 939 - 947
Journal Article
Developmental Biology, ISSN 0012-1606, 10/2014, Volume 394, Issue 1, pp. 142 - 155
Specification of the trophectoderm (TE) and inner cell mass (ICM) lineages in the mouse blastocyst correlates with cell position, as TE derives from outer... 
Trophectoderm | Cell lineage | YAP | Cell polarity | CDX2 | Inner cell mass | LINEAGE DIFFERENTIATION | PREIMPLANTATION EMBRYO | STEM-CELLS | KINASE | EPITHELIAL POLARITY | FATE SPECIFICATION | DEVELOPMENTAL BIOLOGY | BINDING PROTEIN RHO | YAP PATHWAY | rho GTP-Binding Proteins - antagonists & inhibitors | Tumor Suppressor Proteins - antagonists & inhibitors | rho-Associated Kinases - antagonists & inhibitors | Ectoderm - metabolism | RNA Interference | rho-Associated Kinases - metabolism | Gene Expression Regulation, Developmental | Tumor Suppressor Proteins - genetics | Mice, Inbred DBA | Cell Differentiation | Protein-Serine-Threonine Kinases - metabolism | Amides - pharmacology | Homeodomain Proteins - biosynthesis | Nanog Homeobox Protein | Phosphoproteins - biosynthesis | Signal Transduction | Intracellular Signaling Peptides and Proteins - antagonists & inhibitors | Mice, Inbred C57BL | Enzyme Inhibitors - pharmacology | Protein-Serine-Threonine Kinases - genetics | Transcription Factors - biosynthesis | Protein Kinase C - antagonists & inhibitors | Cell Lineage | Animals | Blastocyst Inner Cell Mass - metabolism | Homeodomain Proteins - antagonists & inhibitors | rho GTP-Binding Proteins - metabolism | Cell Polarity - physiology | Adaptor Proteins, Signal Transducing - biosynthesis | Mice | Pyridines - pharmacology | RNA, Small Interfering | CDX2 Transcription Factor | G proteins | Index Medicus | trophectoderm | cell polarity | cell lineage
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 2016, Volume 25, Issue 24, pp. 5365 - 5382
Mutations in leucine-rich repeat kinase 2 (LRRK2) cause late-onset, autosomal dominant familial Parkinsons disease (PD) and variation at the LRRK2 locus... 
MICROTUBULE STABILITY | DOMAIN | AUTOSOMAL-DOMINANT PARKINSONISM | GENE | REPEAT KINASE 2 | PHOSPHORYLATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | MUTATION | GENETICS & HEREDITY | DOPAMINERGIC-NEURONS | ALPHA-SYNUCLEIN | GTP-BINDING | Phosphorylation | Proteome - genetics | Dopaminergic Neurons - pathology | Humans | Drosophila melanogaster - genetics | Drosophila Proteins - biosynthesis | Protein Interaction Maps | Brain - metabolism | Drosophila melanogaster - metabolism | Syntaxin 1 - genetics | Dopaminergic Neurons - metabolism | Phosphoric Monoester Hydrolases - biosynthesis | Nerve Tissue Proteins - biosynthesis | Parkinson Disease - metabolism | Syntaxin 1 - biosynthesis | Synaptic Vesicles - genetics | Disease Models, Animal | Parkinson Disease - pathology | Phosphoric Monoester Hydrolases - genetics | Synaptotagmin I - biosynthesis | Animals, Genetically Modified | Gene Expression Regulation | Parkinson Disease - genetics | Synaptotagmin I - genetics | Nerve Tissue Proteins - genetics | rab3 GTP-Binding Proteins - genetics | Animals | rab3 GTP-Binding Proteins - biosynthesis | Leucine-Rich Repeat Serine-Threonine Protein Kinase-2 - biosynthesis | Brain - pathology | Drosophila Proteins - genetics | Mutation | Leucine-Rich Repeat Serine-Threonine Protein Kinase-2 - genetics | Index Medicus | Life Sciences | Human health and pathology
Journal Article
Journal Article
Journal Article
Journal of Cell Biology, ISSN 0021-9525, 2014, Volume 207, Issue 4, pp. 453 - 462
Synaptic demise and accumulation of dysfunctional proteins are thought of as common features in neurodegeneration. However, the mechanisms by which synaptic... 
ENDOSOMES | GENE | NEUROTRANSMITTER RELEASE | DROSOPHILA-MELANOGASTER | COLOR | TRAFFICKING | DEEP-ORANGE | GENOME | CELL BIOLOGY | Synaptic Vesicles - metabolism | Synaptic Transmission - physiology | Membrane Glycoproteins - metabolism | rab5 GTP-Binding Proteins - biosynthesis | Neuromuscular Junction - metabolism | Humans | rab GTP-Binding Proteins - genetics | Drosophila Proteins - metabolism | Drosophila melanogaster - genetics | Endosomes - metabolism | Drosophila Proteins - biosynthesis | Intellectual Disability - genetics | DNA-Binding Proteins - metabolism | Drosophila melanogaster - metabolism | Lysosomes - metabolism | Proteolysis | Craniofacial Abnormalities - genetics | rab GTP-Binding Proteins - metabolism | R-SNARE Proteins - genetics | Neurodegenerative Diseases - genetics | Hearing Loss, Sensorineural - genetics | Neurodegenerative Diseases - metabolism | DNA-Binding Proteins - genetics | Nails, Malformed - genetics | Protein Transport | Carrier Proteins - genetics | Pyridinium Compounds - pharmacology | Animals | Carrier Proteins - metabolism | Hand Deformities, Congenital - genetics | R-SNARE Proteins - biosynthesis | Drosophila Proteins - genetics | Mutation | Quaternary Ammonium Compounds - pharmacology | Nervous system | Degeneration | Genetic aspects | Research | Gene mutations | Proteins | Neurotransmitters | Insects | Neurodegeneration | Epilepsy | Medical screening | Index Medicus
Journal Article
American Journal of Physiology - Lung Cellular and Molecular Physiology, ISSN 1040-0605, 01/2015, Volume 308, Issue 1, pp. L33 - L47
Mutation of threonine for isoleucine at codon 73 (I73T) in the human surfactant protein C (hSP-C) gene (SFTPC) accounts for a significant portion of SFTPC... 
Surfactant protein | Pulmonary fibrosis | Alveolar epithelium | Autophagy | Amphisome | alveolar epithelium | autophagy | amphisome | surfactant protein | pulmonary fibrosis | DOMAIN | PHYSIOLOGY | SURFACTANT PROTEIN-C | AGGRESOME FORMATION | ENDOPLASMIC-RETICULUM STRESS | RAT TYPE-II | LYSOSOMAL STORAGE DISORDERS | EPITHELIAL-CELLS | MULTIVESICULAR BODIES | RESPIRATORY SYSTEM | PULMONARY-FIBROSIS | Proteostasis Deficiencies - metabolism | Lung Diseases, Interstitial - metabolism | Vacuoles - ultrastructure | Lung Diseases, Interstitial - pathology | Microtubule-Associated Proteins - genetics | Sequestosome-1 Protein | Humans | Lysosomes - genetics | Genetic Diseases, Inborn - genetics | Infant | rab GTP-Binding Proteins - genetics | Genetic Diseases, Inborn - pathology | Mutation, Missense | Mitochondria - ultrastructure | Lysosomes - metabolism | ATP-Binding Cassette Transporters - genetics | Mitochondria - genetics | HEK293 Cells | ATP-Binding Cassette Transporters - metabolism | Membrane Potential, Mitochondrial - genetics | Female | Genetic Diseases, Inborn - metabolism | Microfilament Proteins - genetics | Vacuoles - genetics | Gene Expression Regulation - genetics | Proteostasis Deficiencies - pathology | Pulmonary Surfactant-Associated Protein C - metabolism | Mitochondria - metabolism | Microtubule-Associated Proteins - biosynthesis | rab GTP-Binding Proteins - biosynthesis | Ubiquitin-Protein Ligases - biosynthesis | Lysosomes - ultrastructure | Autophagy-Related Protein 8 Family | Proteostasis Deficiencies - genetics | Microfilament Proteins - biosynthesis | Lung Diseases, Interstitial - genetics | Adaptor Proteins, Signal Transducing - genetics | Pulmonary Surfactant-Associated Protein C - genetics | Vacuoles - metabolism | Adaptor Proteins, Signal Transducing - biosynthesis | Ubiquitin-Protein Ligases - genetics | Amino Acid Substitution | Autophagy (Cytology) | Usage | Genetic aspects | Epithelium | Health aspects | Lung diseases | Proteins | ABC transporters | Mutation | Biomass | Surfactants | Cells | Index Medicus | Call for Papers
Journal Article