Search references for DYSBINDIN. Phrases containing DYSBINDIN
See searches and references containing DYSBINDIN!DYSBINDIN
Protein
Dysbindin, short for dystrobrevin-binding protein 1, is a protein constituent of the dystrophin-associated protein complex (DPC) of skeletal muscle cells
Dysbindin
Area of study for clinical research
antipsychotic clozapine. Dysbindin is a protein coded for by the gene DTNBP1, which has been linked to schizophrenia.[citation needed] Dysbindin may be involved
Animal_model_of_schizophrenia
Structure in the basal ganglia of the brain
reduced dysbindin expression. Increased NMDA receptors may point to the involvement of glutamate-dopamine interactions in schizophrenia. Dysbindin, which
Substantia_nigra
Symptom of mental disorders
FOXP2 (which is linked to a familial language disorder and autism) and dysbindin 1 genes43,44. This distal explanation not only does not explain clanging
Clanging
Medical condition
Hohoff, Christa; Birosova, Eva; Arolt, Volker; Baune, Bernhard T. (2011). "Dysbindin (DTNBP1) – A role in psychotic depression?". Journal of Psychiatric Research
Psychotic_depression
Medical condition
AP3B1 gene. HPS type 7 may result from a mutation in the gene coding for dysbindin protein. HPS1, AP3B1, HPS3, HPS4, HPS5, HPS6, DTNBP1 and Biogenesis of
Hermansky–Pudlak_syndrome
identified protein subunits of BLOC-1 include: pallidin muted (protein) dysbindin cappuccino (protein) snapin BLOS1 BLOS2 BLOS3 Ultracentrifugation coupled
Biogenesis of lysosome-related organelles complex 1
Biogenesis_of_lysosome-related_organelles_complex_1
Protein-coding gene in the species Homo sapiens
determined. PLDN has been shown to interact with: BLOC1S1, BLOC1S2, CNO, Dysbindin, MUTED, SNAPAP, and STX12. GRCh38: Ensembl release 89: ENSG00000104164
PLDN
Brooke–Spiegler syndrome Cylindroma DHCR7 Smith–Lemli–Opitz syndrome DTNBP1 Dysbindin Hermansky–Pudlak syndrome type 7 Dyskerin Dyskeratosis congenita ECM1
List of genes mutated in cutaneous conditions
List_of_genes_mutated_in_cutaneous_conditions
Capacity of neurons to regulate their own excitability relative to network activity
symptoms observed in schizophrenic patients, specifically in problems with dysbindin. This dysregulation contribute to the cognitive deficits and delusions
Homeostatic_plasticity
Risk factors related to schizophrenia
reviews suggested that the evidence was strongest for two genes known as dysbindin (DTNBP1) and neuregulin (NRG1), and that a number of other genes (such
Risk_factors_of_schizophrenia
Childhood-onset schizophrenia
indicated in children diagnosed with schizophrenia that include: neuregulin, dysbindin, D-amino acid oxidase, proline dehydrogenase, catechol-Omethyltransferase
Childhood_schizophrenia
Protein-coding gene in the species Homo sapiens
dock vesicles. SNAPAP has been shown to interact with: BLOC1S1, BLOC1S2, Dysbindin, PLDN, RGS7, SNAP-25, SNAP23, and TRPV1. GRCh38: Ensembl release 89: ENSG00000143553
SNAPAP
Human chromosome
CCCTC-binding factor-like CTNNBL1: Beta-catenin-like protein 1 DBNDD2: Dysbindin domain-containing protein 2 DDX27: DEAD box polypeptide 27 DEFB118, DEFB119
Chromosome_20
Single nucleotide polymorphism in human HTR2A gene
V. E. (2012). "Polymorphism of serotonin receptor genes (5-HTR2A) and dysbindin (DTNBP1) and individual components of short-term verbal memory processes
Rs6313
Protein-coding gene in the species Homo sapiens
HIV-1 genes. TRIM32 has been shown to interact with: actin, ABI2 c-Myc, dysbindin, and piasy, Currently, TRIM32 is believed to employ two different mechanisms
TRIM32
Protein-coding gene in the species Homo sapiens
Dysbindin domain-containing protein 2 is a protein that in humans is encoded by the DBNDD2 gene. GRCh38: Ensembl release 89: ENSG00000244274 – Ensembl
DBNDD2
Protein-coding gene in the species Homo sapiens
reading frame for this gene. MUTED has been shown to interact with BLOC1S2, Dysbindin and PLDN. GRCh38: Ensembl release 89: ENSG00000188428 – Ensembl, May 2017
MUTED
Protein-coding gene in the species Homo sapiens
(2003). "Hermansky-Pudlak syndrome type 7 (HPS-7) results from mutant dysbindin, a member of the biogenesis of lysosome-related organelles complex 1 (BLOC-1)"
BLOC1S2
British biochemist
Benson M.A., Newey S.E., Martin-Rendon E., Hawkes R. and Blake D.J. (2001) Dysbindin, a novel coiled-coil containing protein that interacts with the dystrobrevins
Derek_Blake
Protein-coding gene in humans
magnitude. On the contrary, proteins being homologous to CK1BP (e.g. dysbindin or BLOC-1 [biogenesis of lysosome-related organelles complex-1]) are able
CSNK1D
Israeli psychiatrist and researcher
association of schizophrenia with genetic variation in the 6p22. 3 gene, dysbindin, in sib-pair families with linkage and in an additional sample of triad
Bernard_Lerer
Protein
additional to α-dystrobrevin-binding proteins: β-synemin, syncoilin, and dysbindin. Syncoilin and β-synemin are both intermediate filament proteins. The
Dystrobrevin
Protein-coding gene in humans
(2003). "Hermansky-Pudlak syndrome type 7 (HPS-7) results from mutant dysbindin, a member of the biogenesis of lysosome-related organelles complex 1 (BLOC-1)"
BLOC1S4
Protein-coding gene in the species Homo sapiens
Starcevic M, Spencer MJ, Dell'Angelica EC (2006). "Reinvestigation of the dysbindin subunit of BLOC-1 (biogenesis of lysosome-related organelles complex-1)
Dystrobrevin_beta
DYSBINDIN
DYSBINDIN
DYSBINDIN
DYSBINDIN
Female
English
Variant spelling of English Maureen, MAVREENA means "obstinacy, rebelliousness" or "their rebellion."
Girl/Female
Indian
Treasure
Boy/Male
Indian
Gold coin
Boy/Male
American, Australian, Nigerian
Strength; Power of God
Boy/Male
Arabic
Sun of the Faith
Girl/Female
French
A feminine form of John: God is gracious. Famous Bearer: 15th-century French heroine Jeanne d'Arc...
Boy/Male
Tamil
Sacred, Holy, Divine, Another name of Lord Shiva
Boy/Male
Indian
Emancipated; God of Salvation; Absolution; Freedom
Boy/Male
Muslim
Lord, King (1)
Girl/Female
Hindu
Juhi flower
DYSBINDIN
DYSBINDIN
DYSBINDIN
DYSBINDIN
DYSBINDIN