Cited by 200MicroRNA in disease regulationSchizophrenia research and treatmentCancer-related molecular mechanisms research

Validation of schizophrenia-associated genes CSMD1, C10orf26, CACNA1C and TCF4 as miR-137 targets

Kwon, E, Wang, W, Tsai, L-H·2013·Molecular Psychiatry

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Crossref · 10.1038/mp.2011.170

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9 of 9 references verified0 citation errors · 0 not checkable

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  • miR-137 is a key regulator of neuronal development with roles in neurogenesis and maturation and is highly expressed at synapses in the cortex and hippocampus.

    “miR-137 is a key regulator of neuronal development with roles in neurogenesis and maturation 64,65 and is highly expressed at synapses in the cortex and hippocampus. 66”

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Authors
Kwon, E., Wang, W., & Tsai, L.-H.
Affiliations
  • Massachusetts Institute of Technology (US)
  • Broad Institute (US)
Corresponding author
Tsai, L-H
Venue
Molecular Psychiatry
Published
2011-12-20
Volume
18
Issue
1
Pages
11-12
ISSN
  • 1359-4184 (ISSN-L)
  • 1476-5578
OpenAlex
W1979612171
Cited by
200
References
9
Citations by year
2026: 2 · 2024: 9 · 2023: 4 · 2022: 11 · 2021: 11 · 2020: 12 · 2019: 16 · 2018: 12 · 2017: 10 · 2016: 20 · 2015: 23 · 2014: 39 · 2013: 17 · 2012: 14
FWCI
7.55
Type
journal article
Language
en
Open access
closed
Locations
  • Molecular Psychiatry (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › MicroRNA in disease regulation
  • Health Sciences › Medicine › Psychiatry and Mental health › Schizophrenia research and treatment
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer-related molecular mechanisms research
Keywords
schizophrenia, microRNA-137, CSMD1, CACNA1C, TCF4, miRNA target genes, post-transcriptional regulation, copy number variation, microRNA dysregulation
MeSH terms
Transcription Factor 4, DNA Mutational Analysis, Genetic Testing, Humans, Membrane Proteins, Schizophrenia, Transcription Factors, Sequence Analysis, DNA, Calcium Channels, L-Type, Tumor Suppressor Proteins, MicroRNAs, Intracellular Signaling Peptides and Proteins, Basic Helix-Loop-Helix Leucine Zipper Transcription Factors, Genome-Wide Association Study

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