Recommendations for the investigation of animal models of Prader–Willi syndrome
Published 2013 View Full Article
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Title
Recommendations for the investigation of animal models of Prader–Willi syndrome
Authors
Keywords
Derive Cell Line, Contiguous Gene, Ensembl Genome Browser, Postnatal Growth Retardation, Syndrome Association
Journal
MAMMALIAN GENOME
Volume 24, Issue 5-6, Pages 165-178
Publisher
Springer Nature
Online
2013-04-22
DOI
10.1007/s00335-013-9454-2
References
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Note: Only part of the references are listed.- Magel2 Is Required for Leptin-Mediated Depolarization of POMC Neurons in the Hypothalamic Arcuate Nucleus in Mice
- (2013) Rebecca E. Mercer et al. PLoS Genetics
- Energy homeostasis in Prader-Willi Syndrome: How clinical research informs studies of animal models of genetic obesity
- (2012) Rebecca E. Mercer et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Loss of the Prader–Willi obesity syndrome protein necdin promotes adipogenesis
- (2012) Jason Russell Bush et al. GENE
- Prader-Willi syndrome
- (2012) Suzanne B. Cassidy et al. GENETICS IN MEDICINE
- The imprinted NPAP1/C15orf2 gene in the Prader–Willi syndrome region encodes a nuclear pore complex associated protein
- (2012) Lisa C. Neumann et al. HUMAN MOLECULAR GENETICS
- Long Noncoding RNAs with snoRNA Ends
- (2012) Qing-Fei Yin et al. MOLECULAR CELL
- The SNORD115 (H/MBII-52) and SNORD116 (H/MBII-85) gene clusters at the imprinted Prader-Willi locus generate canonical box C/D snoRNAs
- (2012) M.-L. Bortolin-Cavaille et al. NUCLEIC ACIDS RESEARCH
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- (2012) Kazushiro Fujiwara et al. PLoS One
- An Unexpected Function of the Prader-Willi Syndrome Imprinting Center in Maternal Imprinting in Mice
- (2012) Mei-Yi Wu et al. PLoS One
- Mechanisms of activation of the paternally expressed genes by the Prader-Willi imprinting center in the Prader-Willi/Angelman syndromes domains
- (2012) S. Rabinovitz et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Temporal and developmental requirements for the Prader-Willi imprinting center
- (2012) A. J. DuBose et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Nutritional phases in Prader-Willi syndrome
- (2011) Jennifer L. Miller et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Global deficits in development, function, and gene expression in the endocrine pancreas in a deletion mouse model of Prader-Willi syndrome
- (2011) Mihaela Stefan et al. AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM
- Impact of induced pluripotent stem cells on the study of central nervous system disease
- (2011) Paige E Cundiff et al. CURRENT OPINION IN GENETICS & DEVELOPMENT
- Impaired Hypothalamic Regulation of Endocrine Function and Delayed Counterregulatory Response to Hypoglycemia inMagel2-Null Mice
- (2011) Alysa A. Tennese et al. ENDOCRINOLOGY
- A new deletion refines the boundaries of the murine Prader-Willi syndrome imprinting center
- (2011) A. J. DuBose et al. HUMAN MOLECULAR GENETICS
- A guide to analysis of mouse energy metabolism
- (2011) Matthias H Tschöp et al. NATURE METHODS
- Necdin Protects Embryonic Motoneurons from Programmed Cell Death
- (2011) Julianne Aebischer et al. PLoS One
- Transcription Is Required to Establish Maternal Imprinting at the Prader-Willi Syndrome and Angelman Syndrome Locus
- (2011) Emily Y. Smith et al. PLoS Genetics
- Neurobehavioral phenotype in Prader-Willi syndrome
- (2010) Joyce Whittington et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS
- Prader-Willi syndrome and Angelman syndrome
- (2010) Karin Buiting AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS
- Loss of Necdin impairs myosin activation and delays cell polarization
- (2010) Jason R. Bush et al. GENESIS
- The snoRNA MBII-52 (SNORD 115) is processed into smaller RNAs and regulates alternative splicing
- (2010) Shivendra Kishore et al. HUMAN MOLECULAR GENETICS
- A single postnatal injection of oxytocin rescues the lethal feeding behaviour in mouse newborns deficient for the imprinted Magel2 gene
- (2010) Fabienne Schaller et al. HUMAN MOLECULAR GENETICS
- Induced Pluripotent Stem Cells Can Be Used to Model the Genomic Imprinting Disorder Prader-Willi Syndrome
- (2010) Jiayin Yang et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Necdin Promotes Tangential Migration of Neocortical Interneurons from Basal Forebrain
- (2010) T. Kuwajima et al. JOURNAL OF NEUROSCIENCE
- Neurodevelopmental disorders involving genomic imprinting at human chromosome 15q11–q13
- (2010) Stormy J. Chamberlain et al. NEUROBIOLOGY OF DISEASE
- Neonatal Maternal Deprivation Response and Developmental Changes in Gene Expression Revealed by Hypothalamic Gene Expression Profiling in Mice
- (2010) Feng Ding et al. PLoS One
- Induced pluripotent stem cell models of the genomic imprinting disorders Angelman and Prader–Willi syndromes
- (2010) Stormy J. Chamberlain et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Improving Bioscience Research Reporting: The ARRIVE Guidelines for Reporting Animal Research
- (2010) Carol Kilkenny et al. PLOS BIOLOGY
- Regionally reduced brain volume, altered serotonin neurochemistry, and abnormal behavior in mice null for the circadian rhythm output geneMagel2
- (2009) Rebecca E. Mercer et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS
- Necdin restricts proliferation of hematopoietic stem cells during hematopoietic regeneration
- (2009) Y. Kubota et al. BLOOD
- Behavioural and cognitive abnormalities in an imprinting centre deletion mouse model for PraderâWilli syndrome
- (2009) Dinko Relkovic et al. EUROPEAN JOURNAL OF NEUROSCIENCE
- Loss of the imprinted snoRNA mbii-52 leads to increased 5htr2c pre-RNA editing and altered 5HT2CR-mediated behaviour
- (2009) Christine M. Doe et al. HUMAN MOLECULAR GENETICS
- Imprinting regulates mammalian snoRNA-encoding chromatin decondensation and neuronal nucleolar size
- (2009) Karen N. Leung et al. HUMAN MOLECULAR GENETICS
- Necdin is expressed in cachectic skeletal muscle to protect fibers from tumor-induced wasting
- (2009) C. Sciorati et al. JOURNAL OF CELL SCIENCE
- Atp10a, a gene adjacent to the PWS/AS gene cluster, is not imprinted in mouse and is insensitive to the PWS-IC
- (2009) Amanda J. DuBose et al. NEUROGENETICS
- Loss of Magel2, a Candidate Gene for Features of Prader-Willi Syndrome, Impairs Reproductive Function in Mice
- (2009) Rebecca E. Mercer et al. PLoS One
- Breathing deficits of the Prader-Willi syndrome
- (2009) Sebastien Zanella et al. RESPIRATORY PHYSIOLOGY & NEUROBIOLOGY
- Loss of the Prader‐Willi syndrome protein necdin causes defective migration, axonal outgrowth, and survival of embryonic sympathetic neurons
- (2008) Alysa A. Tennese et al. DEVELOPMENTAL DYNAMICS
- Necdin, a Prader-Willi syndrome candidate gene, regulates gonadotropin-releasing hormone neurons during development
- (2008) N. L.G. Miller et al. HUMAN MOLECULAR GENETICS
- Recommendations for the Diagnosis and Management of Prader-Willi Syndrome
- (2008) A. P. Goldstone et al. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
- Necdin Plays a Role in the Serotonergic Modulation of the Mouse Respiratory Network: Implication for Prader-Willi Syndrome
- (2008) S. Zanella et al. JOURNAL OF NEUROSCIENCE
- Necdin Regulates p53 Acetylation via Sirtuin1 to Modulate DNA Damage Response in Cortical Neurons
- (2008) K. Hasegawa et al. JOURNAL OF NEUROSCIENCE
- SnoRNA Snord116 (Pwcr1/MBII-85) Deletion Causes Growth Deficiency and Hyperphagia in Mice
- (2008) Feng Ding et al. PLoS One
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