Found: 18
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Whole-exome sequencing confirms implication of VPS13D as a potential cause of progressive spastic ataxia.
- Published in:
- 2022
- By:
- Publication type:
- journal article
Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders.
- Published in:
- Nature Genetics, 2007, v. 39, n. 1, p. 25, doi. 10.1038/ng1933
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- Publication type:
- Article
Mesenchymal Stem Cell Therapy Stimulates Endogenous Host Progenitor Cells to Improve Colonic Epithelial Regeneration.
- Published in:
- PLoS ONE, 2013, v. 8, n. 7, p. 1, doi. 10.1371/journal.pone.0070170
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- Publication type:
- Article
Selection of an adjuvant for seasonal influenza vaccine in elderly people: modelling immunogenicity from a randomized trial.
- Published in:
- BMC Infectious Diseases, 2013, v. 13, n. 1, p. 1, doi. 10.1186/1471-2334-13-348
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- Publication type:
- Article
Selection of an adjuvant for seasonal influenza vaccine in elderly people: modelling immunogenicity from a randomized trial.
- Published in:
- 2013
- By:
- Publication type:
- journal article
In vivo animal studies help achieve international consensus on standards and guidelines for health risk estimates for chronic exposure to low levels of tritium in drinking water.
- Published in:
- Environmental & Molecular Mutagenesis, 2018, v. 59, n. 7, p. 586, doi. 10.1002/em.22200
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- Publication type:
- Article
Risk of Developing Non-Cancerous Central Nervous System Diseases Due to Ionizing Radiation Exposure during Adulthood: Systematic Review and Meta-Analyses.
- Published in:
- Brain Sciences (2076-3425), 2022, v. 12, n. 8, p. 984, doi. 10.3390/brainsci12080984
- By:
- Publication type:
- Article
The Planar Polarity Protein Scribble1 Is Essential for Neuronal Plasticity and Brain Function.
- Published in:
- Journal of Neuroscience, 2010, v. 30, n. 29, p. 9738, doi. 10.1523/JNEUROSCI.6007-09.2010
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- Publication type:
- Article
New practical definitions for the diagnosis of autosomal recessive spastic ataxia of Charlevoix-Saguenay.
- Published in:
- 2015
- By:
- Publication type:
- journal article
Targeted Dorsal Dentate Gyrus or Whole Brain Irradiation in Juvenile Mice Differently Affects Spatial Memory and Adult Hippocampal Neurogenesis.
- Published in:
- Biology (2079-7737), 2021, v. 10, n. 3, p. 192, doi. 10.3390/biology10030192
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- Publication type:
- Article
The intellectual disability PAK3 R67C mutation impacts cognitive functions and adult hippocampal neurogenesis.
- Published in:
- Human Molecular Genetics, 2020, v. 29, n. 12, p. 1950, doi. 10.1093/hmg/ddz296
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- Publication type:
- Article
Baseline prevalence and type distribution of human papillomavirus in healthy Chinese women aged 18-25 years enrolled in a clinical trial.
- Published in:
- International Journal of Cancer, 2014, v. 135, n. 11, p. 2604, doi. 10.1002/ijc.28896
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- Publication type:
- Article
Autosomal Dominant MPAN: Mosaicism Expands the Clinical Spectrum to Atypical Late‐Onset Phenotypes.
- Published in:
- Movement Disorders, 2023, v. 38, n. 11, p. 2103, doi. 10.1002/mds.29576
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- Publication type:
- Article
Influenza symptoms and their impact on elderly adults: randomised trial of AS03-adjuvanted or non-adjuvanted inactivated trivalent seasonal influenza vaccines.
- Published in:
- Influenza & Other Respiratory Viruses, 2014, v. 8, n. 4, p. 452, doi. 10.1111/irv.12245
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- Publication type:
- Article
Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: A Gradient of Severity in Cognitive Impairments.
- Published in:
- PLoS Genetics, 2014, v. 10, n. 9, p. 1, doi. 10.1371/journal.pgen.1004580
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- Publication type:
- Article
CYP2U1 activity is altered by missense mutations in hereditary spastic paraplegia 56.
- Published in:
- Human Mutation, 2018, v. 39, n. 1, p. 140, doi. 10.1002/humu.23359
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- Publication type:
- Article
Genetic variations of the melatonin pathway in patients with attention-deficit and hyperactivity disorders.
- Published in:
- Journal of Pineal Research, 2011, v. 51, n. 4, p. 394, doi. 10.1111/j.1600-079X.2011.00902.x
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- Publication type:
- Article
An investigation of ribosomal protein L10 gene in autism spectrum disorders.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 1, doi. 10.1186/1471-2350-10-7
- By:
- Publication type:
- Article