المؤلفون: Loring KE; Intellectual Disability Research, Adelaide Medical School, The University of Adelaide, Adelaide, SA, Australia; Robinson Research Institute, The University of Adelaide, Adelaide, SA, Australia., Mattiske T; Intellectual Disability Research, Adelaide Medical School, The University of Adelaide, Adelaide, SA, Australia; Robinson Research Institute, The University of Adelaide, Adelaide, SA, Australia., Lee K; Intellectual Disability Research, Adelaide Medical School, The University of Adelaide, Adelaide, SA, Australia; Robinson Research Institute, The University of Adelaide, Adelaide, SA, Australia., Zysk A; Intellectual Disability Research, Adelaide Medical School, The University of Adelaide, Adelaide, SA, Australia; Robinson Research Institute, The University of Adelaide, Adelaide, SA, Australia., Jackson MR; Intellectual Disability Research, Adelaide Medical School, The University of Adelaide, Adelaide, SA, Australia; Robinson Research Institute, The University of Adelaide, Adelaide, SA, Australia., Noebels JL; Department of Neurology, Baylor College of Medicine, Houston, USA., Shoubridge C; Intellectual Disability Research, Adelaide Medical School, The University of Adelaide, Adelaide, SA, Australia; Robinson Research Institute, The University of Adelaide, Adelaide, SA, Australia. Electronic address: cheryl.shoubridge@adelaide.edu.au.

المصدر: Neurobiology of disease [Neurobiol Dis] 2021 Jun; Vol. 153, pp. 105329. Date of Electronic Publication: 2021 Mar 10.

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

بيانات الدورية: Publisher: Academic Press Country of Publication: United States NLM ID: 9500169 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1095-953X (Electronic) Linking ISSN: 09699961 NLM ISO Abbreviation: Neurobiol Dis Subsets: MEDLINE

مواضيع طبية MeSH: Behavior, Animal/*drug effects , Estradiol/*pharmacology , Estrogens/*pharmacology , Gene Expression Regulation/*drug effects , Homeodomain Proteins/*genetics , Seizures/*genetics , Transcription Factors/*genetics, Animals ; Animals, Newborn ; Early Medical Intervention ; Gene Expression Regulation/genetics ; Humans ; Infant, Newborn ; Intellectual Disability/genetics ; Intellectual Disability/physiopathology ; Mice ; Neurodevelopmental Disorders/genetics ; Peptides/genetics ; Seizures/physiopathology ; Spasms, Infantile/genetics ; Spasms, Infantile/physiopathology