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The Journal of neuroscience : the official journal of the Society for Neuroscience, ISSN 0270-6474, 10/2018, Volume 38, Issue 41, pp. 8822 - 8830
Prediction errors are critical for associative learning. In the brain, these errors are thought to be signaled, in part, by midbrain dopamine neurons. However,... 
associative learning | prediction error | rat | ventral tegmental area | dopamine | conditioned inhibition | PREDICTION ERRORS | ROSTROMEDIAL TEGMENTAL NUCLEUS | REWARDS | ASSOCIATIONS | LATERAL HABENULA | SIGNALS | STIMULI | NEUROSCIENCES | RESPONSES | OPTOGENETIC INHIBITION | REINFORCEMENT | Brain | Dopamine | Inhibitors | Mesencephalon | Neurons | Salience | Associative learning | Inhibition | Conditioning | s
Journal Article
Nucleic Acids Research, ISSN 0305-1048, 10/2009, Volume 38, Issue 1, pp. D457 - D462
Journal Article
PLoS ONE, ISSN 1932-6203, 06/2013, Volume 8, Issue 6, pp. e65088 - e65088
Journal Article
Investigative Ophthalmology and Visual Science, ISSN 0146-0404, 08/2018, Volume 59, Issue 10, pp. 4238 - 4248
PURPOSE. To assess residual cone structure in subjects with mutations in exon 2, 3, and 4 of the OPN1LW or OPN1MW opsin. METHODS. Thirteen males had their... 
Color blindness | Retinal imaging | Myopia | Photoreceptor | DYSFUNCTION SYNDROME | photoreceptor | ADAPTIVE OPTICS | HIGH MYOPIA | RELIABILITY | retinal imaging | DENSITY-MEASUREMENTS | color blindness | VARIABILITY | REPEATABILITY | PHOTORECEPTOR STRUCTURE | DISEASE | myopia | OPHTHALMOLOGY | LINKAGE | Index Medicus | Retina
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 02/2012, Volume 90, Issue 2, pp. 247 - 259
X-linked megalocornea (MGC1) is an ocular anterior segment disorder characterized by an increased cornea diameter and deep anterior chamber evident at birth... 
EYE | WATER DIFFUSION | BONE MORPHOGENETIC PROTEIN | ACQUISITION | GENETICS & HEREDITY | BIOMETRY | UPDATE | ISCEV STANDARD | CHORDIN | LINKAGE | BRAIN | Anterior Eye Segment - embryology | Cerebral Palsy - metabolism | Humans | Middle Aged | Eye Abnormalities - embryology | Genetic Diseases, X-Linked - complications | Molecular Sequence Data | Corneal Diseases - metabolism | Male | Retina - embryology | Anterior Eye Segment - abnormalities | Intellectual Disability - genetics | Intellectual Disability - metabolism | Young Adult | Corneal Diseases - genetics | Genes, X-Linked | Base Sequence | Nerve Tissue Proteins - biosynthesis | Adult | Female | Genetic Diseases, X-Linked - genetics | Eye Proteins - genetics | Megalencephaly - genetics | DNA Copy Number Variations - genetics | Megalencephaly - metabolism | Genetic Diseases, X-Linked - metabolism | Eye Abnormalities - genetics | Nerve Tissue Proteins - genetics | Genetic Diseases, X-Linked - embryology | Phenotype | Pedigree | Retina - abnormalities | Brain - pathology | Cornea - abnormalities | Mutation | Quantitative Trait Loci | Cerebral Palsy - genetics | Eye Abnormalities - complications | Eye Proteins - biosynthesis | Brain | Gene mutations | Genetic variation | Physiological aspects | Causes of | Corneal diseases | Retina | Genetic aspects | Research | Ophthalmology | Proteins | Cornea | Genetic disorders | Morphology | Cognitive ability | Genetic research | Gene expression | Index Medicus
Journal Article
PLoS ONE, ISSN 1932-6203, 08/2014, Volume 9, Issue 8, pp. e104163 - e104163
We describe novel CHRDL1 mutations in ten families with X-linked megalocornea (MGC1). Our mutation-positive cohort enabled us to establish ultrasonography as a... 
CHROMOSOME | POPULATION | MENTAL-RETARDATION SYNDROME | MULTIDISCIPLINARY SCIENCES | BUPHTHALMOS | LTBP2 | DIFFERENTIATION | HYPOGONADISM | PRIMARY CONGENITAL GLAUCOMA | GENOME-WIDE ASSOCIATION | CUL4B GENE | Corneal Diseases - diagnostic imaging | Megalencephaly - diagnostic imaging | Humans | Middle Aged | Child, Preschool | Intellectual Disability - complications | Male | Intellectual Disability - genetics | Young Adult | Corneal Diseases - genetics | Genes, X-Linked | Ultrasonography | Adult | Epilepsy - genetics | Female | Genetic Diseases, X-Linked - diagnostic imaging | Genetic Diseases, X-Linked - genetics | Eye Proteins - genetics | Cerebral Palsy - diagnostic imaging | Megalencephaly - genetics | Muscle Hypotonia - complications | Genetic Predisposition to Disease | Eye Diseases, Hereditary - diagnostic imaging | Muscle Hypotonia - genetics | Genetic Association Studies | Intellectual Disability - diagnostic imaging | Mutation - genetics | Glaucoma - congenital | Nerve Tissue Proteins - genetics | Epilepsy - complications | Eye Diseases, Hereditary - genetics | Exome - genetics | Phenotype | Pedigree | Adolescent | Family | Glaucoma - genetics | Cerebral Palsy - genetics | Corneal Pachymetry | Glaucoma | Phenotypes | Cornea | Intellectual disabilities | Health risks | Genomes | Single-nucleotide polymorphism | Epidemiology | Loci | Eye | Proteins | Missense mutation | Etiology | Diagnostic software | Genetics | Diagnostic systems | Mutation | Bioinformatics | Chromosomes | Polymorphism | Index Medicus
Journal Article
Human Mutation, ISSN 1059-7794, 01/2018, Volume 39, Issue 1, pp. 80 - 91
Journal Article