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LMT USV Toolbox, a Novel Methodological Approach to Place Mouse Ultrasonic Vocalizations in Their Behavioral Contexts—A Study in Female and Male C57BL/6J Mice and in Shank3 Mutant Females.
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- Frontiers in Behavioral Neuroscience, 2021, v. 15, p. 1, doi. 10.3389/fnbeh.2021.735920
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- Article
Altered spinogenesis in iPSC-derived cortical neurons from patients with autism carrying de novo SHANK3 mutations.
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- Scientific Reports, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41598-018-36993-x
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- Article
Crystal structure and functional mapping of human ASMT, the last enzyme of the melatonin synthesis pathway.
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- Journal of Pineal Research, 2013, v. 54, n. 1, p. 46, doi. 10.1111/j.1600-079X.2012.01020.x
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- Article
Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: A Gradient of Severity in Cognitive Impairments.
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- PLoS Genetics, 2014, v. 10, n. 9, p. 1, doi. 10.1371/journal.pgen.1004580
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- Article
Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders.
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- PLoS Genetics, 2012, v. 8, n. 2, p. 1, doi. 10.1371/journal.pgen.1002521
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- Article
A chimeric mouse model to study human iPSC-derived neurons: the case of a truncating SHANK3 mutation.
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- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-70056-4
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- Article
Heterogeneous Pattern of Selective Pressure for PRRT2 in Human Populations, but No Association with Autism Spectrum Disorders.
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- PLoS ONE, 2014, v. 9, n. 3, p. 1, doi. 10.1371/journal.pone.0088600
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- Article
Variations of the Candidate SEZ6L2 Gene on Chromosome 16p11.2 in Patients with Autism Spectrum Disorders and in Human Populations.
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- PLoS ONE, 2011, v. 6, n. 3, p. 1, doi. 10.1371/journal.pone.0017289
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- Article
Identification of Pathway-Biased and Deleterious Melatonin Receptor Mutants in Autism Spectrum Disorders and in the General Population.
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- PLoS ONE, 2010, v. 5, n. 7, p. 1, doi. 10.1371/journal.pone.0011495
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- Article
Both rare and common genetic variants contribute to autism in the Faroe Islands.
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- NPJ Genomic Medicine, 2019, v. 4, n. 1, p. N.PAG, doi. 10.1038/s41525-018-0075-2
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- Article
Both rare and common genetic variants contribute to autism in the Faroe Islands.
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- NPJ Genomic Medicine, 2019, v. 4, n. 1, p. N.PAG, doi. 10.1038/s41525-018-0075-2
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- Article
11q24.2-25 Micro-Rearrangements in Autism Spectrum Disorders: Relation to Brain Structures.
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- American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 12, p. 3019, doi. 10.1002/ajmg.a.37345
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- Article
Decreased phenol sulfotransferase activities associated with hyperserotonemia in autism spectrum disorders.
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- Translational Psychiatry, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41398-020-01125-5
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- Article