| review article | Q7318358 |
| scholarly article | Q13442814 |
| P50 | author | Josef P Kapfhammer | Q86239699 |
| P2093 | author name string | Etsuko Shimobayashi | |
| P2860 | cites work | Deletion at ITPR1 underlies ataxia in mice and spinocerebellar ataxia 15 in humans | Q21092490 |
| Human inositol 1,4,5-trisphosphate type-1 receptor, InsP3R1: structure, function, regulation of expression and chromosomal localization | Q24528268 | ||
| Carbonic anhydrase-related protein is a novel binding protein for inositol 1,4,5-trisphosphate receptor type 1 | Q24529951 | ||
| Cell biology of spinocerebellar ataxia | Q26829511 | ||
| CA8 mutations cause a novel syndrome characterized by ataxia and mild mental retardation with predisposition to quadrupedal gait | Q27312310 | ||
| The gene mutated in ataxia-ocular apraxia 1 encodes the new HIT/Zn-finger protein aprataxin | Q28190324 | ||
| Heterozygous deletion of ITPR1, but not SUMF1, in spinocerebellar ataxia type 16 | Q28252934 | ||
| Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel | Q28300848 | ||
| Single tottering mutations responsible for the neuropathic phenotype of the P-type calcium channel | Q28510345 | ||
| Deranged calcium signaling and neurodegeneration in spinocerebellar ataxia type 3 | Q28575230 | ||
| RORalpha coordinates reciprocal signaling in cerebellar development through sonic hedgehog and calcium-dependent pathways | Q28584730 | ||
| Absence epilepsy in tottering mutant mice is associated with calcium channel defects | Q28587452 | ||
| Inositol trisphosphate and calcium signalling mechanisms | Q29012316 | ||
| The polyglutamine expansion in spinocerebellar ataxia type 6 causes a beta subunit-specific enhanced activation of P/Q-type calcium channels in Xenopus oocytes. | Q30175691 | ||
| A point mutation in TRPC3 causes abnormal Purkinje cell development and cerebellar ataxia in moonwalker mice | Q30486893 | ||
| Development of a multiplex ligation-dependent probe amplification assay for diagnosis and estimation of the frequency of spinocerebellar ataxia type 15. | Q33441126 | ||
| Carbonic anhydrase-related protein VIII antibodies and paraneoplastic cerebellar degeneration | Q33831472 | ||
| Loss of Purkinje cells in the PKCgamma H101Y transgenic mouse | Q33836298 | ||
| Inositol trisphosphate receptor Ca2+ release channels. | Q33983069 | ||
| Protein kinase C gamma (PKC gamma): function of neuron specific isotype | Q34157744 | ||
| Models of IP3 and Ca2+ oscillations: frequency encoding and identification of underlying feedbacks | Q34524742 | ||
| Death and survival of heterozygous Lurcher Purkinje cells in vitro | Q34570847 | ||
| Carbonic anhydrase-related protein VIII deficiency is associated with a distinctive lifelong gait disorder in waddles mice | Q34589910 | ||
| Role of inositol 1,4,5-trisphosphate receptors in pathogenesis of Huntington's disease and spinocerebellar ataxias | Q34981549 | ||
| Do mutations in the murine ataxia gene TRPC3 cause cerebellar ataxia in humans? | Q35054430 | ||
| Molecular mechanism of Spinocerebellar Ataxia type 6: glutamine repeat disorder, channelopathy and transcriptional dysregulation. The multifaceted aspects of a single mutation. | Q35087285 | ||
| Protein kinase C: its role in activity-dependent Purkinje cell dendritic development and plasticity | Q35543663 | ||
| The mutant Moonwalker TRPC3 channel links calcium signaling to lipid metabolism in the developing cerebellum | Q35613348 | ||
| Protection from ataxia-linked apoptosis by gap junction inhibitors | Q36082552 | ||
| The InsP3 receptor: its role in neuronal physiology and neurodegeneration | Q36257714 | ||
| Protein kinase C gamma-mediated phosphorylation of GluA1 in the postsynaptic density of spinal dorsal horn neurons accompanies neuropathic pain, and dephosphorylation by calcineurin is associated with prolonged analgesia | Q36299923 | ||
| Chronic suppression of inositol 1,4,5-triphosphate receptor-mediated calcium signaling in cerebellar purkinje cells alleviates pathological phenotype in spinocerebellar ataxia 2 mice | Q36315976 | ||
| Human ataxias: a genetic dissection of inositol triphosphate receptor (ITPR1)-dependent signaling | Q36384774 | ||
| Molecular pathogenesis of spinocerebellar ataxias. | Q36448937 | ||
| RORalpha, a pivotal nuclear receptor for Purkinje neuron survival and differentiation: from development to ageing | Q36526378 | ||
| Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia | Q36535853 | ||
| Pathogenesis of severe ataxia and tremor without the typical signs of neurodegeneration | Q36652552 | ||
| Carbonic anhydrase related protein 8 mutation results in aberrant synaptic morphology and excitatory synaptic function in the cerebellum | Q36737609 | ||
| Ataxia and epileptic seizures in mice lacking type 1 inositol 1,4,5-trisphosphate receptor. | Q36788552 | ||
| Spinocerebellar ataxias: an update | Q36874869 | ||
| A Restricted Repertoire of De Novo Mutations in ITPR1 Cause Gillespie Syndrome with Evidence for Dominant-Negative Effect | Q36891473 | ||
| Two novel alleles of tottering with distinct Ca(v)2.1 calcium channel neuropathologies | Q37079538 | ||
| Emerging pathogenic pathways in the spinocerebellar ataxias | Q37289638 | ||
| Deranged calcium signaling and neurodegeneration in spinocerebellar ataxia type 2. | Q37359666 | ||
| Early onset of ataxia in moonwalker mice is accompanied by complete ablation of type II unipolar brush cells and Purkinje cell dysfunction. | Q37381862 | ||
| Dendrite formation of cerebellar Purkinje cells | Q37612937 | ||
| An update on carbonic anhydrase-related proteins VIII, X and XI. | Q38072086 | ||
| Disturbed calcium signaling in spinocerebellar ataxias and Alzheimer's disease | Q38408049 | ||
| Roles of inositol 1,4,5-trisphosphate receptors in spinocerebellar ataxias. | Q38717172 | ||
| Spinocerebellar ataxia: relationship between phenotype and genotype - a review | Q38843338 | ||
| Functional characterization of the P1059L mutation in the inositol 1,4,5-trisphosphate receptor type 1 identified in a Japanese SCA15 family. | Q39521359 | ||
| An ITPR1 gene deletion causes spinocerebellar ataxia 15/16: a genetic, clinical and radiological description | Q39673940 | ||
| Mutant protein kinase C gamma that causes spinocerebellar ataxia type 14 (SCA14) is selectively degraded by autophagy. | Q39714056 | ||
| Protein kinase C gamma, a protein causative for dominant ataxia, negatively regulates nuclear import of recessive-ataxia-related aprataxin. | Q39832024 | ||
| Activation of mutant protein kinase Cgamma leads to aberrant sequestration and impairment of its cellular function | Q39978583 | ||
| Role of plasma membrane calcium ATPase isoform 2 in neuronal function in the cerebellum and spinal cord | Q40221598 | ||
| Recessive and Dominant De Novo ITPR1 Mutations Cause Gillespie Syndrome | Q41368463 | ||
| Spinocerebellar ataxia type 6 protein aggregates cause deficits in motor learning and cerebellar plasticity. | Q41679065 | ||
| Hormone-induced calcium oscillations depend on cross-coupling with inositol 1,4,5-trisphosphate oscillations | Q41747572 | ||
| The plasma membrane Ca2+-ATPase2 (PMCA2) is involved in the regulation of Purkinje cell dendritic growth in cerebellar organotypic slice cultures | Q42093052 | ||
| Cav2.1 in cerebellar Purkinje cells regulates competitive excitatory synaptic wiring, cell survival, and cerebellar biochemical compartmentalization. | Q42501141 | ||
| PKC gamma mutations in spinocerebellar ataxia type 14 affect C1 domain accessibility and kinase activity leading to aberrant MAPK signaling. | Q42660284 | ||
| Motor discoordination in mutant mice heterozygous for the type 1 inositol 1,4,5-trisphosphate receptor | Q43596186 | ||
| Altered calcium dynamics in cultured cerebellar cells from IP3R1-deficient mice | Q43815911 | ||
| Regulation of the phosphorylation of the inositol 1,4,5-trisphosphate receptor by protein kinase C. | Q44926929 | ||
| Phenotypical spectrum of cerebellar ataxia associated with a novel mutation in the CA8 gene, encoding carbonic anhydrase (CA) VIII. | Q46134686 | ||
| Aggregate formation of mutant protein kinase C gamma found in spinocerebellar ataxia type 14 impairs ubiquitin-proteasome system and induces endoplasmic reticulum stress | Q46898841 | ||
| Abnormal cerebellar development and ataxia in CARP VIII morphant zebrafish | Q47073764 | ||
| Calcium signaling molecules in human cerebellum at midgestation and in ataxia | Q48230326 | ||
| Sporadic infantile-onset spinocerebellar ataxia caused by missense mutations of the inositol 1,4,5-triphosphate receptor type 1 gene | Q48270136 | ||
| Substrate phosphorylation in the protein kinase Cgamma knockout mouse | Q48304498 | ||
| Activation of class I metabotropic glutamate receptors limits dendritic growth of Purkinje cells in organotypic slice cultures | Q48343887 | ||
| Inositol 1,4,5-trisphosphate receptor type 1 in granule cells, not in Purkinje cells, regulates the dendritic morphology of Purkinje cells through brain-derived neurotrophic factor production. | Q48392771 | ||
| Bergmann glia expression of polyglutamine-expanded ataxin-7 produces neurodegeneration by impairing glutamate transport | Q48435478 | ||
| Immunohistochemical localization of an inositol 1,4,5-trisphosphate receptor, P400, in neural tissue: studies in developing and adult mouse brain | Q48704992 | ||
| Increased protein kinase C gamma activity induces Purkinje cell pathology in a mouse model of spinocerebellar ataxia 14. | Q48711246 | ||
| P/Q-type and T-type calcium channels, but not type 3 transient receptor potential cation channels, are involved in inhibition of dendritic growth after chronic metabotropic glutamate receptor type 1 and protein kinase C activation in cerebellar Purk | Q48763035 | ||
| Mutant PKCγ in spinocerebellar ataxia type 14 disrupts synapse elimination and long-term depression in Purkinje cells in vivo. | Q48859186 | ||
| Expression of type 1 inositol 1,4,5-trisphosphate receptor during axogenesis and synaptic contact in the central and peripheral nervous system of developing rat. | Q49101768 | ||
| Mutant gammaPKC found in spinocerebellar ataxia type 14 induces aggregate-independent maldevelopment of dendrites in primary cultured Purkinje cells. | Q50611131 | ||
| Protein kinase C activity modulates dendritic differentiation of rat Purkinje cells in cerebellar slice cultures. | Q51392587 | ||
| Enzymological analysis of mutant protein kinase Cgamma causing spinocerebellar ataxia type 14 and dysfunction in Ca2+ homeostasis. | Q51788908 | ||
| Carbonic Anhydrase 8 Expression in Purkinje Cells Is Controlled by PKCγ Activity and Regulates Purkinje Cell Dendritic Growth. | Q52148923 | ||
| Impaired synapse elimination during cerebellar development in PKC gamma mutant mice. | Q52204081 | ||
| Identification and characterization of PKCγ, a kinase associated with SCA14, as an amyloidogenic protein. | Q54322709 | ||
| The clinical and genetic spectrum of spinocerebellar ataxia 14 | Q56908924 | ||
| Protein kinase C gamma mutations in spinocerebellar ataxia 14 increase kinase activity and alter membrane targeting | Q81196143 | ||
| P275 | copyright license | Creative Commons Attribution-NonCommercial | Q6936496 |
| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | cell | Q7868 |
| enzyme | Q8047 | ||
| nervous system | Q9404 | ||
| spinocerebellar ataxia | Q899726 | ||
| Purkinje cell | Q1570272 | ||
| spinocerebellar degenerations | Q66124188 | ||
| P5008 | on focus list of Wikimedia project | ScienceSource | Q55439927 |
| P304 | page(s) | 151-159 | |
| P577 | publication date | 2018-01-01 | |
| 2018-01-30 | |||
| P1433 | published in | Current Neuropharmacology | Q20181354 |
| P1476 | title | Calcium Signaling, PKC Gamma, IP3R1 and CAR8 Link Spinocerebellar Ataxias and Purkinje Cell Dendritic Development | |
| P478 | volume | 16 |
| Q89985788 | Atm deficiency in the DNA polymerase β null cerebellum results in cerebellar ataxia and Itpr1 reduction associated with alteration of cytosine methylation |
| Q89926585 | Cerebellum-enriched protein INPP5A contributes to selective neuropathology in mouse model of spinocerebellar ataxias type 17 |
| Q92354437 | Disrupted Calcium Signaling in Animal Models of Human Spinocerebellar Ataxia (SCA) |
| Q49666213 | Inositol 1,4,5-trisphosphate receptors and neurodegenerative disorders |
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