المؤلفون: Bhalla, Kritika, Rosier, Karen, Monnens, Yenthe, Meulemans, Sandra, Vervoort, Ellen, Thorrez, Lieven, Agostinis, Patrizia, Meier, Daniel T., Rochtus, Anne, Resnick, James L., Creemers, John W.M.

المصدر: In BBA - Molecular Basis of Disease June 2024 1870(5)

المؤلفون: Coulson, Rochelle L, Powell, Weston T, Yasui, Dag H, Dileep, Gayathri, Resnick, James, LaSalle, Janine M

المصدر: Human Molecular Genetics. 27(23)

مصطلحات موضوعية: Biological Sciences, Genetics, Mental Health, Rare Diseases, Biotechnology, Brain Disorders, Neurosciences, Intellectual and Developmental Disabilities (IDD), Neurological, Alleles, Alternative Splicing, Animals, Brain, Cell Nucleolus, DNA-Binding Proteins, Disease Models, Animal, Genomic Imprinting, Humans, In Situ Hybridization, Fluorescence, Male, Mice, Transgenic, Nerve Tissue Proteins, Neurons, Nuclear Proteins, Prader-Willi Syndrome, RNA, Small Nucleolar, Sequence Deletion, Sleep, Medical and Health Sciences, Genetics & Heredity

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/2xw3q9r4

المؤلفون: Yazdi, Puya G, Su, Hailing, Ghimbovschi, Svetlana, Fan, Weiwei, Coskun, Pinar E, Nalbandian, Angèle, Knoblach, Susan, Resnick, James L, Hoffman, Eric, Wallace, Douglas C, Kimonis, Virginia E

المصدر: Clinical and Translational Science. 6(5)

مصطلحات موضوعية: Paediatrics, Biomedical and Clinical Sciences, Intellectual and Developmental Disabilities (IDD), Pediatric, Obesity, Rare Diseases, Nutrition, Genetics, Congenital Structural Anomalies, Brain Disorders, 2.1 Biological and endogenous factors, Metabolic and endocrine, Animals, Brain, Disease Models, Animal, Electron Transport Chain Complex Proteins, Gene Expression Profiling, Gene Expression Regulation, Gene Regulatory Networks, Genome, Genomic Imprinting, Mice, Mitochondria, Muscles, Oligonucleotide Array Sequence Analysis, Prader-Willi Syndrome, RNA, Messenger, Reproducibility of Results, Sequence Deletion, Prader-Willi syndrome, differential gene expression, PWS-IC mouse model, Cardiorespiratory Medicine and Haematology, Oncology and Carcinogenesis, Other Medical and Health Sciences, General Clinical Medicine, Cardiovascular medicine and haematology, Pharmacology and pharmaceutical sciences

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/09n63237
https://escholarship.org/content/qt09n63237/qt09n63237.pdf

المؤلفون: Leung, Karen N, Vallero, Roxanne O, DuBose, Amanda J, Resnick, James L, LaSalle, Janine M

المصدر: Human Molecular Genetics. 18(22)

مصطلحات موضوعية: Genetics, Mental Health, Congenital Structural Anomalies, Autism, Rare Diseases, Intellectual and Developmental Disabilities (IDD), Brain Disorders, Neurosciences, Pediatric, 1.1 Normal biological development and functioning, Underpinning research, Neurological, Adult, Animals, Cell Nucleolus, Chromatin, Chromatin Assembly and Disassembly, Chromosomes, Mammalian, Genomic Imprinting, Humans, Male, Mice, Mice, Inbred C57BL, Middle Aged, Neurons, Prader-Willi Syndrome, RNA, Small Nucleolar, Ubiquitin-Protein Ligases, snRNP Core Proteins, Biological Sciences, Medical and Health Sciences, Genetics & Heredity

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/4pn7g9tf

المؤلفون: Lewis, Michael W., Brant, Jason O., Kramer, Joseph M., Moss, James I., Yang, Thomas P., Hansen, Peter J., Williams, R. Stan, Resnick, James L.

المصدر: Proceedings of the National Academy of Sciences of the United States of America, 2015 Jun 01. 112(22), 6871-6875.

URL الوصول: https://www.jstor.org/stable/26463466

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المؤلفون: Lim, Chae Ho, Brower, Jeffrey V.^{Aff1, Aff2}, Resnick, James L., Oh, S. Paul, Terada, Naohiro^Aff1

المصدر: Reproductive Sciences. 22(2):250-257

المؤلفون: DuBose, Amanda J., Smith, Emily Y., Johnstone, Karen A., Resnick, James L.

المصدر: Proceedings of the National Academy of Sciences of the United States of America, 2012 Feb . 109(9), 3446-3450.

URL الوصول: https://www.jstor.org/stable/41506970

المؤلفون: Pellikaan, Karlijn, Woerden, Geeske M. van, Kleinendorst, Lotte, Rosenberg, Anna G. W., Horsthemke, Bernhard, Grosser, Christian, Zutven, Laura J. C. M. van, Rossum, Elisabeth F. C. van, Lely, Aart J. van der, Resnick, James L., Brüggenwirth, Hennie T., Haelst, Mieke M. van, Graaff, Laura C. G. de

المصدر: Genes
Volume 12
Issue 6

مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, brain, genetic variation, nutritional and metabolic diseases, genetics, prader–willi syndrome, nervous system diseases, genomic imprinting

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=multidiscipl::03cf6704aadd865536820419d81bb35f

المؤلفون: Sussman, Raquel, Resnick, James, Calame, Kathryn, Baluch, John

المصدر: Proceedings of the National Academy of Sciences of the United States of America, 1978 Dec 01. 75(12), 5817-5821.

URL الوصول: https://www.jstor.org/stable/68848