Pages that link to "Q35341465"
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The following pages link to Knockout of G protein β5 impairs brain development and causes multiple neurologic abnormalities in mice (Q35341465):
Displayed 29 items.
- Disruption of G-protein γ5 subtype causes embryonic lethality in mice (Q28509591) (← links)
- G protein beta 5 is targeted to D2-dopamine receptor-containing biochemical compartments and blocks dopamine-dependent receptor internalization (Q28542580) (← links)
- GNB5 mutation causes a novel neuropsychiatric disorder featuring attention deficit hyperactivity disorder, severely impaired language development and normal cognition (Q28975772) (← links)
- Regulator of G protein signaling 6 (RGS6) protein ensures coordination of motor movement by modulating GABAB receptor signaling. (Q30505394) (← links)
- Potential translational targets revealed by linking mouse grooming behavioral phenotypes to gene expression using public databases. (Q34076537) (← links)
- Ablation of the GNB3 gene in mice does not affect body weight, metabolism or blood pressure, but causes bradycardia. (Q34160902) (← links)
- An allosteric regulator of R7-RGS proteins influences light-evoked activity and glutamatergic waves in the inner retina (Q35070141) (← links)
- Focal exposure of limited lung volumes to high-dose irradiation down-regulated organ development-related functions and up-regulated the immune response in mouse pulmonary tissues. (Q35906384) (← links)
- Defective retinal depolarizing bipolar cells in regulators of G protein signaling (RGS) 7 and 11 double null mice. (Q35922662) (← links)
- Regulators of G protein signaling RGS7 and RGS11 determine the onset of the light response in ON bipolar neurons. (Q35974073) (← links)
- Expression of the Gβ5/R7-RGS protein complex in pituitary and pancreatic islet cells (Q36069404) (← links)
- Subcellular localization of regulator of G protein signaling RGS7 complex in neurons and transfected cells. (Q36087249) (← links)
- GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability. (Q37230697) (← links)
- Differential localization of G protein βγ subunits. (Q37731597) (← links)
- Regulation of neurite morphogenesis by interaction between R7 regulator of G protein signaling complexes and G protein subunit Gα13. (Q38706526) (← links)
- The Gβ5 protein regulates sensitivity to TRAIL-induced cell death in colon carcinoma (Q38973682) (← links)
- A central role for R7bp in the regulation of itch sensation (Q40353644) (← links)
- G-protein genomic association with normal variation in gray matter density (Q40653111) (← links)
- Genome-Wide Screen for Genes Involved in Caenorhabditis elegans Developmentally Timed Sleep (Q41385120) (← links)
- Expression profile of G-protein βγ subunit gene transcripts in the mouse olfactory sensory epithelia (Q41457292) (← links)
- Quantitative Multiple-Reaction Monitoring Proteomic Analysis of Gβ and Gγ Subunits in C57Bl6/J Brain Synaptosomes. (Q47843802) (← links)
- Gβ2 Regulates the Multipolar-Bipolar Transition of Newborn Neurons in the Developing Neocortex (Q48249727) (← links)
- A High-Throughput Time-Resolved Fluorescence Energy Transfer Assay to Screen for Modulators of RGS7/Gβ5/R7BP Complex. (Q52320595) (← links)
- Activation of β- and α2-adrenergic receptors stimulate tubulin polymerization and promote the association of Gβγ with microtubules in cultured NIH3T3 cells. (Q54977534) (← links)
- G-protein-coupled receptor signaling and neural tube closure defects. (Q55014626) (← links)
- A NGS-Targeted Autism/ID Panel Reveals Compound Heterozygous GNB5 Variants in a Novel Patient (Q60958172) (← links)
- GPCR regulation of secretion (Q90590562) (← links)
- The Emerging Role of Gβ Subunits in Human Genetic Diseases (Q91809881) (← links)
- Genetic characterization and long-term management of severely affected siblings with intellectual developmental disorder with cardiac arrhythmia syndrome (Q91843123) (← links)