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Journal Article
Current Pharmaceutical Design, ISSN 1381-6128, 2012, Volume 18, Issue 25, pp. 3653 - 3662
Journal Article
Neuron, ISSN 0896-6273, 07/2015, Volume 87, Issue 1, pp. 4 - 6
The brain regulates blood flow to match energy demand to nutrient supply. In this issue of , using in vivo optical imaging and optogenetics, report that... 
BRAIN-BARRIER | STROKE | NEUROSCIENCES | DISEASE | Brain Ischemia | Animals | Cerebral Cortex - blood supply | Cerebrovascular Circulation - physiology | Humans | Muscle Contraction - physiology | Myocytes, Smooth Muscle - physiology | Pericytes - physiology | Studies | Brain | Smooth muscle | Ischemia | Rodents
Journal Article
Neuron, ISSN 0896-6273, 12/2017, Volume 96, Issue 5, pp. 1055 - 1069.e6
Coordinating angiogenesis with acquisition of tissue-specific properties in endothelial cells is essential for vascular function. In the retina, endothelial... 
Wnt/β-catenin signaling | Caveolin-1 | angiogenesis | blood-retina barrier | Frizzled-4 | transcytosis | vascular pruning | Claudin-5 | Norrin | Apcdd1 | tight junction | Occludin | BRAIN-BARRIER | FENESTRATED ENDOTHELIA | ANGIOGENESIS | ENDOTHELIAL-CELLS | CNS | CENTRAL-NERVOUS-SYSTEM | DIFFERENTIATION | NEUROSCIENCES | NORRIN | BREAKDOWN | INFILTRATION | SOXF Transcription Factors - metabolism | Pericytes - physiology | Retinal Vessels - physiology | Membrane Proteins - physiology | Extracellular Matrix - physiology | Neurons - physiology | HMGB Proteins - metabolism | Intracellular Signaling Peptides and Proteins - genetics | Endothelial Cells - physiology | Tight Junction Proteins - metabolism | Blood-Retinal Barrier - physiology | Endothelial Cells - metabolism | Membrane Proteins - genetics | Neuroglia - physiology | Mice, Transgenic | Intracellular Signaling Peptides and Proteins - biosynthesis | Mutation - genetics | Mice, Knockout | Extracellular Matrix - ultrastructure | Membrane Proteins - biosynthesis | Animals | Wnt Signaling Pathway - drug effects | Endothelium - metabolism | Mice | Intracellular Signaling Peptides and Proteins - physiology | Endothelium - physiology | Neurosciences | Permeability | Cells | Endothelium | Wnt protein | Maturation | Tight junctions | Blood vessels | Retina | Nervous system | Hybridization | Remodeling | Endothelial cells | Angiogenesis | β-catenin | Signaling | Blood-brain barrier | Cellular biology | Pruning | LRP5 protein | Ligands
Journal Article
Nature, ISSN 0028-0836, 04/2010, Volume 464, Issue 7291, pp. 1043 - 1047
Hereditary hypotrichosis simplex is a rare autosomal dominant form of hair loss characterized by hair follicle miniaturization(1,2). Using genetic linkage... 
AUTOSOMAL DOMINANT INHERITANCE | IN-VITRO | ANDROGENETIC ALOPECIA | XENOPUS | PROTEIN-COUPLED RECEPTOR | MULTIDISCIPLINARY SCIENCES | NEURAL-TUBE | DEPENDENT MANNER | EXPRESSION | HAIR-FOLLICLE | SPEMANN ORGANIZER | Cell Proliferation | Membrane Glycoproteins - metabolism | Xenopus Proteins - genetics | Humans | Membrane Glycoproteins - chemistry | Hypotrichosis - genetics | Hair - metabolism | Neurons - cytology | Stem Cells - cytology | Stem Cells - metabolism | Wnt Proteins - metabolism | Hair Follicle - pathology | Point Mutation - genetics | Wnt Proteins - genetics | Cell Differentiation | Neurons - metabolism | Xenopus laevis - genetics | Hypotrichosis - metabolism | Spinal Cord - cytology | Cell Line | Xenopus laevis - embryology | Signal Transduction | Mutant Proteins - genetics | Intracellular Signaling Peptides and Proteins | Genes, Reporter - genetics | Mutant Proteins - metabolism | Chromosome Mapping | Chick Embryo | beta Catenin - metabolism | Membrane Glycoproteins - genetics | Membrane Proteins | Animals | Xenopus Proteins - deficiency | Scalp | Xenopus laevis - metabolism | Hair Follicle - metabolism | Hair Follicle - growth & development | Xenopus Proteins - metabolism | Mice | Skin | Chromosomes, Human, Pair 18 - genetics | Hypotrichosis - pathology | Wnt Proteins - antagonists & inhibitors | Genes, Dominant - genetics | Hair - growth & development | Membrane Glycoproteins - deficiency | Embryonic development | Alopecia | Baldness | Gene mutations | Analysis | Physiological aspects | Genetic aspects | Research | Wnt proteins | Risk factors | Mutation | Hair loss | Genes | Human | Hair | Mutations | Membranes | Inhibitors | Activation | Signalling | hair follicle | APCDD1 | hereditary hypotrichosis | Wnt inhibitor
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Journal Article