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The Lancet Neurology, ISSN 1474-4422, 04/2018, Volume 17, Issue 4, pp. 335 - 346
Journal Article
2010, RSC Nanoscience & Nanotechnology, ISBN 9781847559111, Volume 15, xiv, 318
Aimed predominantly at graduate students, this book provides all the necessary information to conduct experiments in microfluidics and molecular biology.. 
Microfluidic devices | Genomics | Microbial genomics | Life Sciences | Science | General | Chemistry | Biochemistry | Microtechnology - methods
Book
Journal Article
Cerebral Cortex, ISSN 1047-3211, 11/2018, Volume 28, Issue 11, pp. 3994 - 4007
Abstract The retinoic acid-related orphan receptor alpha (RORα) is well-known for its role in cerebellar development and maturation as revealed in staggerer... 
retinoic acid-related receptor | dendrite | axon branching | somatosensory system | thalamus | MONOAMINE-OXIDASE | MUTANT | NEUROTRANSMITTER RELEASE | PURKINJE-CELL LOSS | NEUROSCIENCES | SEROTONIN EXCESS | NEURONAL SUBTYPE SPECIFICATION | SOMATOSENSORY CORTEX | LAYER-IV | STAGGERER MOUSE | EXPRESSION
Journal Article
Journal Article
NMR in Biomedicine, ISSN 0952-3480, 10/2014, Volume 27, Issue 10, p. 1143
  In this article, we report in vivo 1H MRS performed in 1.8-µLvoxels in a mouse model of Down syndrome (DS). To characterise the excitation-inhibition... 
Brain | Medical research | Analysis | Medicine, Experimental | GABA | Down syndrome | Glutamine
Journal Article
Journal Article
Oncogene, ISSN 0950-9232, 2001, Volume 20, Issue 25, pp. 3258 - 3265
  Ewing tumour is characterized by specific chromosome translocations which fuse EWS to a subset of genes encoding ETS transcription factors, most frequently... 
p57 | c-Myc | Ewing tumour | EWS-FLI-1 | Cell cycle
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 2015, Volume 24, Issue 21, pp. 5965 - 5976
Journal Article
Brain Structure and Function, ISSN 1863-2653, 11/2015, Volume 220, Issue 6, pp. 3757 - 3757
Journal Article
PLoS ONE, ISSN 1932-6203, 08/2012, Volume 7, Issue 8, pp. e41616 - e41616
Forty percent of people with Down syndrome exhibit heart defects, most often an atrioventricular septal defect (AVSD) and less frequently a ventricular septal... 
HUMAN FETUSES | SYNDROME PROJECT | ANOMALIES | MOUSE | GENES | HUMAN-CHROMOSOME-21 | BIOLOGY | DEVELOPMENTAL DEFECTS | CONGENITAL HEART-DEFECTS | EXPRESSION | PRIMARY CILIUM | Cell Line | Down Syndrome - pathology | Heart Septal Defects, Ventricular - complications | Heart Septal Defects, Ventricular - genetics | Heart Septal Defects, Ventricular - pathology | Signal Transduction | Chromosomes, Human - genetics | Humans | Transcriptome | Hedgehog Proteins - metabolism | Heart Septal Defects - complications | Heart Septal Defects, Ventricular - metabolism | Young Adult | Lymphocytes - pathology | Phenotype | Animals | Heart Septal Defects - metabolism | Down Syndrome - complications | Heart Septal Defects - pathology | Mice | Heart Septal Defects - genetics | DNA microarrays | Lymphocytes | Genes | Cardiac patients | Down syndrome | Comparative analysis | Gene expression | Heart | Enrichment | Biotechnology | Clathrin | Trisomy | Transcription factors | Tissues | Defects | Cell adhesion & migration | Endocytosis | Pathways | Down's syndrome | Heart diseases | Chromosomes | Deoxyribonucleic acid--DNA | Fetuses | Lymphoblastoid cell lines | Principal components analysis | Cardiomyocytes | Patients | Carriers | Hypotheses | Microtubules | Stem cells | Genetic engineering | Ventricle | Chromosome aberrations | Index Medicus | Deoxyribonucleic acid | DNA
Journal Article