Pages that link to "Q24631638"
Jump to navigation
Jump to search
The following pages link to Hermansky-Pudlak syndrome type 7 (HPS-7) results from mutant dysbindin, a member of the biogenesis of lysosome-related organelles complex 1 (BLOC-1) (Q24631638):
Displaying 50 items.
- Hermansky-Pudlak syndrome (Q1506216) (← links)
- Mutation in archain 1, a subunit of COPI coatomer complex, causes diluted coat color and Purkinje cell degeneration (Q21092441) (← links)
- Association of the Hermansky-Pudlak syndrome type-3 protein with clathrin (Q21284167) (← links)
- Dystrobrevin, beta (Q21496336) (← links)
- Biogenesis of lysosomal organelles complex-1, subunit 6, pallidin (Q21497137) (← links)
- The WASH complex, an endosomal Arp2/3 activator, interacts with the Hermansky-Pudlak syndrome complex BLOC-1 and its cargo phosphatidylinositol-4-kinase type IIα (Q24292907) (← links)
- The schizophrenia susceptibility factor dysbindin and its associated complex sort cargoes from cell bodies to the synapse (Q24293250) (← links)
- DAMAGE, a Novel α-Dystrobrevin-associated MAGE Protein in Dystrophin Complexes (Q24299985) (← links)
- Assembly and architecture of biogenesis of lysosome-related organelles complex-1 (BLOC-1). (Q24300804) (← links)
- Nucleocytoplasmic Shuttling of Dysbindin-1, a Schizophrenia-related Protein, Regulates Synapsin I Expression (Q24301877) (← links)
- Dysbindin-1 is a synaptic and microtubular protein that binds brain snapin (Q24303507) (← links)
- TRIM32 is an E3 ubiquitin ligase for dysbindin (Q24313358) (← links)
- Characterization of BLOC-2, a complex containing the Hermansky-Pudlak syndrome proteins HPS3, HPS5 and HPS6 (Q24317736) (← links)
- Identification of snapin and three novel proteins (BLOS1, BLOS2, and BLOS3/reduced pigmentation) as subunits of biogenesis of lysosome-related organelles complex-1 (BLOC-1) (Q24337584) (← links)
- BLOC-1 is required for cargo-specific sorting from vacuolar early endosomes toward lysosome-related organelles (Q24337651) (← links)
- The dysbindin-containing complex (BLOC-1) in brain: developmental regulation, interaction with SNARE proteins and role in neurite outgrowth (Q24338919) (← links)
- Reinvestigation of the dysbindin subunit of BLOC-1 (biogenesis of lysosome-related organelles complex-1) as a dystrobrevin-binding protein (Q24543935) (← links)
- Clinical and cellular characterisation of Hermansky-Pudlak syndrome type 6 (Q24610520) (← links)
- Schizophrenia susceptibility gene dysbindin regulates glutamatergic and dopaminergic functions via distinctive mechanisms in Drosophila (Q24625434) (← links)
- Genetic interstitial lung disease (Q24626239) (← links)
- Methamphetamine-associated psychosis (Q24632172) (← links)
- Mutant mouse models: genotype-phenotype relationships to negative symptoms in schizophrenia (Q24632939) (← links)
- Melanocyte-specific proteins are aberrantly trafficked in melanocytes of Hermansky-Pudlak syndrome-type 3 (Q24675801) (← links)
- Identification of a homozygous deletion in the AP3B1 gene causing Hermansky-Pudlak syndrome, type 2 (Q24685566) (← links)
- Inherited platelet disorders: toward DNA-based diagnosis (Q26752148) (← links)
- Yeast homologues of three BLOC-1 subunits highlight KxDL proteins as conserved interactors of BLOC-1. (Q27939848) (← links)
- Psychiatric genetics: progress amid controversy (Q28284253) (← links)
- The BLOS1-interacting protein KXD1 is involved in the biogenesis of lysosome-related organelles (Q28510459) (← links)
- Hermansky-Pudlak protein complexes, AP-3 and BLOC-1, differentially regulate presynaptic composition in the striatum and hippocampus (Q28513167) (← links)
- Evidence of novel neuronal functions of dysbindin, a susceptibility gene for schizophrenia (Q28568230) (← links)
- The rat Ruby ( R) locus is Rab38: identical mutations in Fawn-hooded and Tester-Moriyama rats derived from an ancestral Long Evans rat sub-strain (Q28573030) (← links)
- Dysbindin is a potent inducer of RhoA-SRF-mediated cardiomyocyte hypertrophy (Q28575296) (← links)
- Evidence that the BLOC-1 protein dysbindin modulates dopamine D2 receptor internalization and signaling but not D1 internalization (Q28576208) (← links)
- DTNBP1, a schizophrenia susceptibility gene, affects kinetics of transmitter release (Q28586199) (← links)
- Role of dysbindin in dopamine receptor trafficking and cortical GABA function (Q28593127) (← links)
- The schizophrenia susceptibility gene dysbindin regulates dendritic spine dynamics (Q28863274) (← links)
- Melanocytes and their diseases (Q28658506) (← links)
- Impaired long-term memory retention and working memory in sdy mutant mice with a deletion in Dtnbp1, a susceptibility gene for schizophrenia (Q28756538) (← links)
- Practice parameter for the diagnosis and management of primary immunodeficiency (Q29042159) (← links)
- Oculocutaneous albinism type 1: link between mutations, tyrosinase conformational stability, and enzymatic activity. (Q30394454) (← links)
- Neurodevelopmental animal models of schizophrenia: role in novel drug discovery and development (Q30414108) (← links)
- Behavioral characterization of mice overexpressing human dysbindin-1. (Q30428226) (← links)
- Dysbindin-1 modulates prefrontal cortical activity and schizophrenia-like behaviors via dopamine/D2 pathways. (Q30465987) (← links)
- Dysbindin-1 mutant mice implicate reduced fast-phasic inhibition as a final common disease mechanism in schizophrenia (Q30468313) (← links)
- Dysbindin-containing complexes and their proposed functions in brain: from zero to (too) many in a decade. (Q30474256) (← links)
- Review of pathological hallmarks of schizophrenia: comparison of genetic models with patients and nongenetic models (Q30476810) (← links)
- Modeling the positive symptoms of schizophrenia in genetically modified mice: pharmacology and methodology aspects (Q30476813) (← links)
- Combined effect of neonatal immune activation and mutant DISC1 on phenotypic changes in adulthood (Q30477667) (← links)
- Neurobehavioral abnormalities in the dysbindin-1 mutant, sandy, on a C57BL/6J genetic background (Q30481233) (← links)
- Haploinsufficiency of two histone modifier genes on 6p22.3, ATXN1 and JARID2, is associated with intellectual disability (Q30540408) (← links)