|  Help  |  About  |  Contact Us

Search our database by keyword

Examples

  • Search this entire website. Enter identifiers, names or keywords for genes, diseases, strains, ontology terms, etc. (e.g. Pax6, Parkinson, ataxia)
  • Use OR to search for either of two terms (e.g. OR mus) or quotation marks to search for phrases (e.g. "dna binding").
  • Boolean search syntax is supported: e.g. Balb* for partial matches or mus AND NOT embryo to exclude a term

Search results 401 to 409 out of 409 for Gabrb3

<< First    < Previous  |  Next >    Last >>
0.02s
Type Details Score
Genotype
Symbol: Oca2/Oca2
Background: involves: 101/Rl * C3H/Rl
Zygosity: ht
Has Mutant Allele: true
Publication
First Author: Knoll JH
Year: 1993
Journal: Hum Mol Genet
Title: FISH ordering of reference markers and of the gene for the alpha 5 subunit of the gamma-aminobutyric acid receptor (GABRA5) within the Angelman and Prader-Willi syndrome chromosomal regions.
Volume: 2
Issue: 2
Pages: 183-9
Publication
First Author: Buettner VL
Year: 2004
Journal: Mamm Genome
Title: Analysis of imprinting in mice with uniparental duplication of proximal chromosomes 7 and 15 by use of a custom oligonucleotide microarray.
Volume: 15
Issue: 3
Pages: 199-209
Publication  
First Author: Blednov YA
Year: 2024
Journal: Neuropharmacology
Title: The PDE4 inhibitor apremilast modulates ethanol responses in Gabrb1-S409A knock-in mice via PKA-dependent and independent mechanisms.
Volume: 257
Pages: 110035
Publication  
First Author: Yu Z
Year: 2022
Journal: Brain Res Bull
Title: Contextual fear conditioning regulates synapse-related gene transcription in mouse microglia.
Volume: 189
Pages: 57-68
Publication
First Author: Odeh H
Year: 2004
Journal: Audiol Neurootol
Title: Characterization of two transgene insertional mutations at pirouette, a mouse deafness locus.
Volume: 9
Issue: 5
Pages: 303-14
Publication
First Author: Shi SQ
Year: 2015
Journal: Curr Biol
Title: Ube3a imprinting impairs circadian robustness in Angelman syndrome models.
Volume: 25
Issue: 5
Pages: 537-45
Publication
First Author: Odeh H
Year: 2010
Journal: Am J Hum Genet
Title: Mutations in Grxcr1 are the basis for inner ear dysfunction in the pirouette mouse.
Volume: 86
Issue: 2
Pages: 148-60
Publication      
First Author: Oak Ridge National Laboratory
Year: 2005
Journal: Unpublished
Title: Information obtained from the Oak Ridge National Laboratory Mutant Mouse Database (ORNL), Oak Ridge, TN