Associated Papers
Expanding the mutational spectrum of congenital microcephaly in Pakistani families.
Farooq S et al.
Frontiers in Genetics, 2025
41555927 (PubMed )
Supplement: Table1.xlsx › Family_3_ASPM
Molecular and in silico analyses of SYN III gene variants in autism spectrum disorder.
Baris RO et al.
Irish Journal of Medical Science, 2023
The Role of Synapsins in Neurological Disorders.
Mirza FJ et al.
Neuroscience Bulletin, 2018
Synapsin III: role in neuronal plasticity and disease.
Porton B et al.
Seminars in Cell & Developmental Biology, 2011
Association and expression study of synapsin III and schizophrenia.
Chen Q et al.
Neuroscience Letters, 2009
PhosphoPOINT: a comprehensive human kinase interactome and phospho-protein database.
Yang CY et al.
Bioinformatics (oxford, England), 2008
Potential genetic variants in schizophrenia: a Bayesian analysis.
Hall H et al.
The World Journal of Biological Psychiatry : the Official Journal of the World Federation of Societies of Biological Psychiatry, 2007
Analysis of synapsin III-196 promoter mutation in schizophrenia and bipolar disorder.
Lachman HM et al.
Neuropsychobiology, 2006
Association of schizophrenia in African Americans to polymorphism in synapsin III gene.
Lachman HM et al.
Psychiatric Genetics, 2005
Novel human alpha1a-adrenoceptor single nucleotide polymorphisms alter receptor pharmacology and biological function.
Lei B et al.
Naunyn-schmiedeberg's Archives of Pharmacology, 2005
A rare polymorphism affects a mitogen-activated protein kinase site in synapsin III: possible relationship to schizophrenia.
Porton B et al.
Biological Psychiatry, 2004
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