المؤلفون: Anantha Shekhar, Andrei I. Molosh, D. W. Clapp, H. P. Drozd, Jodi L. Lukkes, Stephanie D. Fitz

المصدر: Journal of Neurodevelopmental Disorders
Journal of Neurodevelopmental Disorders, Vol 12, Iss 1, Pp 1-13 (2020)

مصطلحات موضوعية: Male, Mouse, Delay discounting, Cliff avoidance reaction test, Open field, Mice, 0302 clinical medicine, Adrenergic alpha-2 Receptor Agonists, biology, Guanfacine, Inhibition, Psychological, Phenotype, medicine.symptom, medicine.drug, Agonist, medicine.medical_specialty, congenital, hereditary, and neonatal diseases and abnormalities, Impulsivity, Neurofibromatosis 1, Adrenergic receptor, medicine.drug_class, Cognitive Neuroscience, Pathology and Forensic Medicine, lcsh:RC321-571, 03 medical and health sciences, Alpha 2A-adrenergic receptor agonist, Reward, Internal medicine, medicine, Attention deficit hyperactivity disorder, ADHD, Animals, Neurofibromatosis, lcsh:Neurosciences. Biological psychiatry. Neuropsychiatry, neoplasms, business.industry, Research, medicine.disease, Neurofibromin 1, eye diseases, Hyperactivity, 030227 psychiatry, nervous system diseases, Behavioral inhibition, Disease Models, Animal, Endocrinology, Attention Deficit Disorder with Hyperactivity, Pediatrics, Perinatology and Child Health, Impulsive Behavior, biology.protein, Neurology (clinical), business, 030217 neurology & neurosurgery, Neurofibromatosis type 1

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d45f90d406e004b272d779aa117bd8d9Test
http://europepmc.org/articles/PMC6961243Test

المؤلفون: Victor-Felix Mautner, David Neil Cooper, Josef Högel, Lan Kluwe, Tanja Mußotter, Rosa Nguyen, Hildegard Kehrer-Sawatzki

المصدر: BMC Medical Genetics
BMC Medical Genetics, Vol 13, Iss 1, p 98 (2012)

مصطلحات موضوعية: Male, medicine.disease_cause, CDKN2A, CDKN2B, Neurofibroma, Genetics(clinical), Child, Genetics (clinical), Genetics, Mutation, Polycomb Repressive Complex 2, Middle Aged, Neoplasm Proteins, Gene Expression Regulation, Neoplastic, Phenotype, Child, Preschool, Female, RNA, Long Noncoding, Research Article, Adult, lcsh:Internal medicine, congenital, hereditary, and neonatal diseases and abnormalities, Neurofibromatosis 1, lcsh:QH426-470, Adolescent, Genotype, Biology, Polymorphism, Single Nucleotide, Young Adult, Genes, Neurofibromatosis 1, medicine, SNP, Humans, Genetic Predisposition to Disease, Expressivity (genetics), Neurofibromatosis, Allele, lcsh:RC31-1245, neoplasms, Cyclin-Dependent Kinase Inhibitor p16, Genetic Association Studies, Cyclin-Dependent Kinase Inhibitor p15, Neurofibroma, Plexiform, medicine.disease, R1, eye diseases, nervous system diseases, lcsh:Genetics, Cancer research, Gene Deletion, Transcription Factors

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e56efb7db0f3a9476e038c9786cd291Test
https://orca.cardiff.ac.uk/id/eprint/84054Test/1/1471-2350-13-98.pdf

المؤلفون: Yi-Ping Hsueh

المصدر: Journal of Biomedical Science
Journal of Biomedical Science, Vol 19, Iss 1, p 33 (2012)

مصطلحات موضوعية: Dendritic spine, Endocrinology, Diabetes and Metabolism, Clinical Biochemistry, lcsh:Medicine, Cell Cycle Proteins, Review, VCP/p97, Valosin Containing Protein, Morphogenesis, Pharmacology (medical), Neurofibromatosis type I, Adenosine Triphosphatases, Neurons, Neurofibromin 1, Ophthalmoplegia, biology, Neurodegeneration, General Medicine, IBMPFD, Phenotype, Cell biology, Metabolic Networks and Pathways, Frontotemporal dementia, medicine.medical_specialty, congenital, hereditary, and neonatal diseases and abnormalities, Contracture, Neurofibromatosis 1, Valosin-containing protein, Dendritic Spines, Myositis, Inclusion Body, Neurodevelopmental disorder, Internal medicine, medicine, Humans, Protein kinase A, Molecular Biology, Biochemistry, medical, Neurofibromatosis Type I, Biochemistry (medical), lcsh:R, statin, Cell Biology, neurofibromin, medicine.disease, Cyclic AMP-Dependent Protein Kinases, nervous system diseases, Dendritic spine formation, Endocrinology, biology.protein, Hydroxymethylglutaryl-CoA Reductase Inhibitors

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b89fff64f05c709134933b5bd5a6af8Test
http://europepmc.org/articles/PMC3326706Test