المؤلفون: Ciernia, Annie Vogel, Yasui, Dag H, Pride, Michael C, Durbin-Johnson, Blythe, Noronha, Adriana B, Chang, Alene, Knotts, Trina A, Rutkowsky, Jennifer R, Ramsey, Jon J, Crawley, Jacqueline N, LaSalle, Janine M

المصدر: Human Molecular Genetics. 27(23)

مصطلحات موضوعية: Biological Sciences, Genetics, Brain Disorders, Neurosciences, Pediatric, Rett Syndrome, Neurodegenerative, Rare Diseases, 2.1 Biological and endogenous factors, Aetiology, Metabolic and endocrine, Animals, Disease Models, Animal, Exons, Female, Gene Expression Regulation, Heterozygote, Humans, Male, Methyl-CpG-Binding Protein 2, Mice, Motor Activity, Mutation, Phenotype, Protein Isoforms, Medical and Health Sciences, Genetics & Heredity

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/1sz4w1qn

المؤلفون: Ciernia, Annie Vogel, Pride, Michael C, Durbin-Johnson, Blythe, Noronha, Adriana, Chang, Alene, Yasui, Dag H, Crawley, Jacqueline N, LaSalle, Janine M

المصدر: Human Molecular Genetics. 26(10)

مصطلحات موضوعية: Biological Sciences, Genetics, Brain Disorders, Rare Diseases, Rett Syndrome, Neurosciences, Behavioral and Social Science, Pediatric, Intellectual and Developmental Disabilities (IDD), Mental Health, Women's Health, Basic Behavioral and Social Science, Neurodegenerative, Congenital, Animals, Behavior, Animal, Disease Models, Animal, Environment, Female, Genetic Association Studies, Genotype, Heterozygote, Male, Methyl-CpG-Binding Protein 2, Mice, Mice, Knockout, Motor Skills, Phenotype, Medical and Health Sciences, Genetics & Heredity

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/7pf0g8gn
https://escholarship.org/content/qt7pf0g8gn/qt7pf0g8gn.pdf

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المؤلفون: Kerani, Roxanne, Berzkalns, Anna, Chang, Alene, Golden, Matthew R., Moreno, Juan Palacios, Ramchandani, Meena S.

المصدر: Sexually Transmitted Diseases; 2024 Supplement, Vol. 51, pS383-S384, 2p

المؤلفون: Berzkalns, Anna, Chang, Alene, Golden, Matthew R., Kerani, Roxanne, Moreno, Juan Palacios, Ramchandani, Meena S.

المصدر: Sexually Transmitted Diseases; 2024 Supplement, Vol. 51, pS245-S246, 2p

المؤلفون: Vogel Ciernia A; Department of Medical Microbiology and Immunology, UC Davis School of Medicine, University of California, Davis, CA, USA.; UC Davis Genome Center, University of California, Davis, CA, USA.; UC Davis MIND Institute, University of California, Davis, CA, USA., Yasui DH; Department of Medical Microbiology and Immunology, UC Davis School of Medicine, University of California, Davis, CA, USA., Pride MC; UC Davis MIND Institute, University of California, Davis, CA, USA.; Department of Psychiatry and Behavioral Sciences, UC Davis School of Medicine, University of California, Davis, CA, USA., Durbin-Johnson B; Department of Public Health Sciences, UC Davis School of Medicine, University of California, Davis, CA, USA., Noronha AB; Department of Medical Microbiology and Immunology, UC Davis School of Medicine, University of California, Davis, CA, USA., Chang A; Department of Medical Microbiology and Immunology, UC Davis School of Medicine, University of California, Davis, CA, USA., Knotts TA; Department of Molecular Biosciences, UC Davis School of Veterinary Medicine, University of California, Davis, CA, USA., Rutkowsky JR; Department of Molecular Biosciences, UC Davis School of Veterinary Medicine, University of California, Davis, CA, USA., Ramsey JJ; Department of Molecular Biosciences, UC Davis School of Veterinary Medicine, University of California, Davis, CA, USA., Crawley JN; UC Davis MIND Institute, University of California, Davis, CA, USA.; Department of Psychiatry and Behavioral Sciences, UC Davis School of Medicine, University of California, Davis, CA, USA., LaSalle JM; Department of Medical Microbiology and Immunology, UC Davis School of Medicine, University of California, Davis, CA, USA.; UC Davis Genome Center, University of California, Davis, CA, USA.; UC Davis MIND Institute, University of California, Davis, CA, USA.

المصدر: Human molecular genetics [Hum Mol Genet] 2018 Dec 01; Vol. 27 (23), pp. 4077-4093.

نوع المنشور: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE

مواضيع طبية MeSH: Methyl-CpG-Binding Protein 2/*genetics , Motor Activity/*genetics , Rett Syndrome/*genetics, Animals ; Disease Models, Animal ; Exons/genetics ; Female ; Gene Expression Regulation/genetics ; Heterozygote ; Humans ; Male ; Mice ; Motor Activity/physiology ; Mutation ; Phenotype ; Protein Isoforms/genetics ; Rett Syndrome/metabolism ; Rett Syndrome/physiopathology

المؤلفون: Vogel Ciernia A; Medical Microbiology and Immunology.; Genome Center.; MIND Institute., Pride MC; MIND Institute.; Department of Psychiatry and Behavioral Sciences., Durbin-Johnson B; Public Health Sciences., Noronha A; Medical Microbiology and Immunology.; Genome Center.; MIND Institute., Chang A; Medical Microbiology and Immunology.; Genome Center.; MIND Institute., Yasui DH; Medical Microbiology and Immunology.; Genome Center.; MIND Institute.; Department of Psychiatry and Behavioral Sciences., Crawley JN; MIND Institute.; Department of Psychiatry and Behavioral Sciences., LaSalle JM; Medical Microbiology and Immunology.; Genome Center.; MIND Institute.; Department of Psychiatry and Behavioral Sciences.; Center for Children's Environmental Health, University of California, Davis, UC Davis, CA, USA.

المصدر: Human molecular genetics [Hum Mol Genet] 2017 May 15; Vol. 26 (10), pp. 1839-1854.

نوع المنشور: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE

مواضيع طبية MeSH: Rett Syndrome/*diagnosis, Animals ; Behavior, Animal ; Disease Models, Animal ; Environment ; Female ; Genetic Association Studies ; Genotype ; Heterozygote ; Male ; Methyl-CpG-Binding Protein 2/metabolism ; Mice ; Mice, Knockout ; Motor Skills/physiology ; Phenotype ; Rett Syndrome/genetics ; Rett Syndrome/veterinary