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06/2018, Handbook of clinical neurology, ISBN 044463956X, Volume 154, 366
'The Cerebellum' is designed to update the reader on the latest and clinically relevant advances in the study of cerebellar diseases in children and adults. It... 
Neurology | Cerebellum-Diseases | Embryology | Cerebellum
eBook
Human Molecular Genetics, ISSN 0964-6906, 05/2013, Volume 22, Issue 10, pp. 2024 - 2040
Journal Article
Science, ISSN 0036-8075, 11/2003, Volume 302, Issue 5647, pp. 1044 - 1046
Journal Article
Neuron, ISSN 0896-6273, 1997, Volume 19, Issue 3, pp. 547 - 559
Journal Article
PLoS Biology, ISSN 1544-9173, 04/2017, Volume 15, Issue 4, pp. e2001573 - e2001573
All vertebrate brains develop following a common Bauplan defined by anteroposterior (AP) and dorsoventral (DV) subdivisions, characterized by largely conserved... 
DEVELOPMENTAL EXPRESSION PATTERNS | PAIRED BOX GENE | BIOCHEMISTRY & MOLECULAR BIOLOGY | BIOLOGY | IN-SITU HYBRIDIZATION | CHICK-EMBRYO | BRANCHIOSTOMA-LANCEOLATUM | CENTRAL-NERVOUS-SYSTEM | ZINC-FINGER GENE | HOMEOBOX GENE | ISTHMIC ORGANIZER | SONIC-HEDGEHOG | Brain - embryology | Lancelets - metabolism | Embryo, Nonmammalian - metabolism | Vertebrates - embryology | Embryo, Nonmammalian - embryology | In Situ Hybridization, Fluorescence | Male | Zebrafish | Chick Embryo | Mice, Knockout | Biological Evolution | Brain - metabolism | Animals | Gene Expression Regulation, Developmental | Models, Biological | Neural Tube - metabolism | Lancelets - embryology | Models, Genetic | Neural Tube - embryology | Body Patterning - genetics | Vertebrates - metabolism | Cerebellum | Brain | Pattern formation | Regulations | High resolution | Funding | Biological evolution | Colleges & universities | Competitiveness | Central nervous system | Nervous system | Evolutionary genetics | Hybridization | Floating | Inactivation | Visual system | Neural tube | Developmental stages | Technology | Cooperation | Genetics | Spawning behavior | Oceans | Spawning | Gene families | pax2 protein | Topology | Anatomy | Gene expression | Embryos | Editors | Mice | Aberration | Mutation | Visualization | Fibroblast growth factor | Biomedical research | Separation | Methodology | Laboratories | Psychobiology | Circuits | Genes | Science | Editing | Forebrain | Homology | Biology | Visual perception | Evolution | Neural plate | Zinc finger proteins | Supervision | Brain architecture | Markers | Zinc | Medicine | Vertebrates | Brain research | Writing | Diencephalon | Acquisitions & mergers | Tumors | Index Medicus | Biologia molecular | Cervell | Tub neural | Molecular biology | Expressió gènica
Journal Article
Journal Article
Science, ISSN 0036-8075, 1/2013, Volume 339, Issue 6116, pp. 204 - 207
We investigated the role of histone methyltransferase Ezh2 in tangential migration of mouse precerebellar pontine nuclei, the main relay between neocortex and... 
Cerebellum | Phenotypes | Neuroscience | Neurons | REPORTS | Hindbrain | Connectivity | Arrows | In situ hybridization | Progenitor cells | Animal migration behavior | SYSTEM | NETRIN-1 | COMPLEX | HINDBRAIN | GUIDANCE | MULTIDISCIPLINARY SCIENCES | Polycomb Repressive Complex 2 - genetics | Netrin-1 | Epigenesis, Genetic | Homeodomain Proteins - metabolism | Nerve Growth Factors - metabolism | Neural Pathways - physiology | Cerebellum - embryology | Metencephalon - embryology | Gene Expression Regulation, Developmental | Tumor Suppressor Proteins - genetics | Neurons - physiology | Transcription, Genetic | Neural Pathways - embryology | Pons - embryology | Genes, Homeobox | Netrin Receptors | Tumor Suppressor Proteins - metabolism | Cerebellum - metabolism | Receptors, Cell Surface - metabolism | Mice, Transgenic | Enhancer of Zeste Homolog 2 Protein | Animals | Cerebral Cortex - embryology | Nerve Growth Factors - genetics | Cerebellum - cytology | Cerebral Cortex - physiology | Mice | Pons - metabolism | Polycomb Repressive Complex 2 - metabolism | Cell Movement | Pons - cytology | Receptors, Cell Surface - genetics | Histones | Physiological aspects | Pons | Methyltransferases | Properties | Proteins | Epigenetics | Brain | Rodents | Neurobiology | Index Medicus | Genes | Migration | Organizations | Encoding | Position (location) | Streams
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 07/2015, Volume 24, Issue 13, pp. 3732 - 3741
Journal Article
Development, ISSN 0950-1991, 12/1997, Volume 124, Issue 24, pp. 4999 - 5011
Journal Article
Histochemistry and Cell Biology, ISSN 0948-6143, 3/2012, Volume 137, Issue 3, pp. 355 - 366
Journal Article
PLoS ONE, ISSN 1932-6203, 09/2012, Volume 7, Issue 9, pp. e44975 - e44975
Joubert syndrome and related diseases (JSRD) are developmental cerebello-oculo-renal syndromes with phenotypes including cerebellar hypoplasia, retinal... 
RETINAL DEGENERATION | LEBER CONGENITAL AMAUROSIS | MUTATIONS CAUSE | TRANSITION ZONE | SYNDROME-RELATED DISORDERS | MULTIDISCIPLINARY SCIENCES | CILIOPATHY | MICE | NPHP6 GENE | CENTROSOMAL PROTEIN | MECKEL-GRUBER-SYNDROME | Brain - embryology | Kidney - embryology | Genomics | Humans | Eye Abnormalities - embryology | Retina - embryology | Cerebellum - abnormalities | Kidney Diseases, Cystic - embryology | Neoplasm Proteins - metabolism | Brain - metabolism | Kidney - metabolism | Gene Expression Regulation, Developmental | Antigens, Neoplasm - metabolism | Conserved Sequence | Kidney Diseases, Cystic - genetics | Neoplasm Proteins - genetics | Cerebellar Diseases - embryology | Antigens, Neoplasm - genetics | Cell Line | Abnormalities, Multiple | Eye Abnormalities - genetics | Organ Specificity | Centrosome - metabolism | Protein Transport | Animals | Cerebellar Diseases - genetics | Adaptor Proteins, Signal Transducing - genetics | Retina - abnormalities | Mice | Evolution, Molecular | Embryonic development | Gene mutations | Joubert syndrome | Physiological aspects | Development and progression | Genetic aspects | Research | Choroid plexus | Cerebellum | Brain | Syngeneic grafts | Congenital defects | Epithelial cells | Genes | Biological evolution | Central nervous system | Evolutionary genetics | Retina | Nervous system | Neurodevelopmental disorders | Tissues | Defects | Recruitment | Proteins | Ethics | Genotype & phenotype | Hypoplasia | Congenital diseases | Nephronophthisis | Developmental biology | Fetuses | Organs | Gene expression | Embryos | Medicine | Environmental science | Retinal degeneration | Mutation | Kidney diseases | Dystrophy | Position (location) | Kidney transplantation | Index Medicus
Journal Article
Acta Neuropathologica, ISSN 0001-6322, 2/2009, Volume 117, Issue 2, pp. 185 - 200