human | Q5 |
P227 | GND ID | 128594179 |
P2798 | Loop ID | 165504 |
P496 | ORCID iD | 0000-0001-5092-9238 |
P1053 | ResearcherID | W-2094-2018 |
P214 | VIAF ID | 42893615 |
P106 | occupation | researcher | Q1650915 |
P21 | sex or gender | male | Q6581097 |
Q98895548 | A gene therapy for inherited blindness using dCas9-VPR-mediated transcriptional activation |
Q53284086 | A key role for cyclic nucleotide gated (CNG) channels in cGMP-related retinitis pigmentosa. |
Q28592015 | A novel mechanism of modulation of hyperpolarization-activated cyclic nucleotide-gated channels by Src kinase |
Q108792491 | A universal protocol for isolating retinal ON bipolar cells across species via fluorescence-activated cell sorting |
Q38309238 | A30P α-Synuclein interferes with the stable integration of adult-born neurons into the olfactory network |
Q40624978 | AAV Vectors for FRET-Based Analysis of Protein-Protein Interactions in Photoreceptor Outer Segments |
Q36396453 | AAV-Mediated Gene Supplementation Therapy in Achromatopsia Type 2: Preclinical Data on Therapeutic Time Window and Long-Term Effects |
Q41926074 | AAV8 Can Induce Innate and Adaptive Immune Response in the Primate Eye. |
Q63248344 | Abstracts from the 8th International Conference on cGMP Generators, Effectors and Therapeutic Implications : Bamberg, Germany. 23-25 June, 2017 |
Q93000728 | Accessory heterozygous mutations in cone photoreceptor CNGA3 exacerbate CNG channel-associated retinopathy |
Q92301674 | Advancing Gene Therapy for PDE6A Retinitis Pigmentosa |
Q40773439 | Age-dependent levels of 5-methyl-, 5-hydroxymethyl-, and 5-formylcytosine in human and mouse brain tissues |
Q51406935 | Author Response: Possibility of Cytoplasmic Transportation Between Donor-Host Cell Following Photoreceptor Transplantation. |
Q35921402 | CNGA3 deficiency affects cone synaptic terminal structure and function and leads to secondary rod dysfunction and degeneration |
Q60678823 | CNGA3: A Target of Spinal Nitric Oxide/cGMP Signaling and Modulator of Inflammatory Pain Hypersensitivity |
Q94581494 | COVID-19: Ophthalmological Aspects of the SARS-CoV 2 Global Pandemic |
Q36043321 | Cav1.4 L-Type Calcium Channels Contribute to Calpain Activation in Degenerating Photoreceptors of rd1 Mice |
Q85793375 | Characterization of neurite outgrowth and ectopic synaptogenesis in response to photoreceptor dysfunction |
Q35971599 | Contribution of the receptor guanylyl cyclase GC-D to chemosensory function in the olfactory epithelium. |
Q35767902 | Corticotropin-Releasing Hormone Receptor Type 1 (CRHR1) Clustering with MAGUKs Is Mediated via Its C-Terminal PDZ Binding Motif |
Q37352765 | Cyclic nucleotide-gated channels |
Q45875179 | Design and Development of AAV-based Gene Supplementation Therapies for Achromatopsia and Retinitis Pigmentosa. |
Q50959164 | Detection of cGMP in the degenerating retina. |
Q91312282 | Development of Methodology and Study Protocol: Safety and Efficacy of a Single Subretinal Injection of rAAV.hCNGA3 in Patients with CNGA3-Linked Achromatopsia Investigated in an Exploratory Dose-Escalation Trial |
Q47644484 | Disturbed Processing of Contextual Information in HCN3 Channel Deficient Mice |
Q49530211 | Early Microglia Activation Precedes Photoreceptor Degeneration in a Mouse Model of CNGB1-Linked Retinitis Pigmentosa |
Q50438393 | Endoplasmic reticulum (ER) Ca2+-channel activity contributes to ER stress and cone death in cyclic nucleotide-gated channel deficiency. |
Q36002797 | Endoplasmic reticulum stress-associated cone photoreceptor degeneration in cyclic nucleotide-gated channel deficiency |
Q36961180 | Function and dysfunction of CNG channels: insights from channelopathies and mouse models |
Q57987105 | Functional analyses of Pericentrin and Syne-2 interaction in ciliogenesis |
Q47568788 | Gene Supplementation Rescues Rod Function and Preserves Photoreceptor and Retinal Morphology in Dogs, Leading the Way Towards Treating Human PDE6A-Retinitis Pigmentosa |
Q38122108 | Gene replacement therapy for retinal CNG channelopathies |
Q39016569 | Gene therapy for achromatopsia. |
Q45875986 | Gene therapy restores missing cone-mediated vision in the CNGA3-/- mouse model of achromatopsia |
Q42229312 | Gene therapy restores vision and delays degeneration in the CNGB1(-/-) mouse model of retinitis pigmentosa. |
Q45880504 | Gene therapy restores vision and delays degeneration in the CNGB1(-/-) mouse model of retinitis pigmentosa. |
Q45875525 | Gene therapy successfully delays degeneration in a mouse model of PDE6A-linked retinitis pigmentosa (RP 43). |
Q35903255 | HCN1 Channels Enhance Rod System Responsivity in the Retina under Conditions of Light Exposure |
Q48131725 | HCN2 channels in local inhibitory interneurons constrain LTP in the hippocampal direct perforant path |
Q42494063 | HCN3 contributes to the ventricular action potential waveform in the murine heart |
Q88391692 | Hif1a inactivation rescues photoreceptor degeneration induced by a chronic hypoxia-like stress |
Q54231528 | Humoral Immune Response After Intravitreal But Not After Subretinal AAV8 in Primates and Patients. |
Q34991085 | Hyperpolarization-activated cation channels: from genes to function |
Q27330551 | Identification of a common non-apoptotic cell death mechanism in hereditary retinal degeneration |
Q28510666 | Impaired channel targeting and retinal degeneration in mice lacking the cyclic nucleotide-gated channel subunit CNGB1 |
Q46404515 | Impaired opsin targeting and cone photoreceptor migration in the retina of mice lacking the cyclic nucleotide-gated channel CNGA3. |
Q57454499 | In Vitro Evaluation of AAV Vectors for Retinal Gene Therapy |
Q27309205 | In Vivo Analysis of Disease-Associated Point Mutations Unveils Profound Differences in mRNA Splicing of Peripherin-2 in Rod and Cone Photoreceptors |
Q33500921 | In vivo analysis of cone survival in mice |
Q52912786 | In-Depth Functional Diagnostics of Mouse Models by Single-Flash and Flicker Electroretinograms without Adapting Background Illumination. |
Q90874262 | Intrinsic Differential Scanning Fluorimetry for Fast and Easy Identification of Adeno-Associated Virus Serotypes |
Q87578720 | Investigation of the immunogenicity of different types of aggregates of a murine monoclonal antibody in mice |
Q42458324 | Isotope-based analysis of modified tRNA nucleosides correlates modification density with translational efficiency |
Q28504473 | Loss of CNGB1 protein leads to olfactory dysfunction and subciliary cyclic nucleotide-gated channel trapping |
Q40994703 | Loss of HCN1 enhances disease progression in mouse models of CNG channel-linked retinitis pigmentosa and achromatopsia |
Q37153814 | Loss of cone cyclic nucleotide-gated channel leads to alterations in light response modulating system and cellular stress response pathways: a gene expression profiling study |
Q114870690 | Metabolic Analysis of Vitreous/Lens and Retina in Wild Type and Retinal Degeneration Mice |
Q92155135 | Morpho-Rheological Fingerprinting of Rod Photoreceptors Using Real-Time Deformability Cytometry |
Q44909676 | Morphological characterization of the retina of the CNGA3(-/-)Rho(-/-) mutant mouse lacking functional cones and rods |
Q37593044 | Mosaic synaptopathy and functional defects in Cav1.4 heterozygous mice and human carriers of CSNB2. |
Q48235260 | Mosaic synaptopathy and functional defects in Cav1.4 heterozygous mice and human carriers of CSNB2. |
Q92458135 | Mouse brain proteomics establishes MDGA1 and CACHD1 as in vivo substrates of the Alzheimer protease BACE1 |
Q91766711 | Neuropathic and cAMP-induced pain behavior is ameliorated in mice lacking CNGB1 |
Q112724318 | Novel AAV capsids for intravitreal gene therapy of photoreceptor disorders |
Q57454496 | Optimized Subretinal Injection Technique for Gene Therapy Approaches |
Q45883094 | Optimized technique for subretinal injections in mice |
Q54217659 | Optogenetic Control of Neural Circuits in the Mongolian Gerbil. |
Q33729317 | Pathological α-synuclein impairs adult-born granule cell development and functional integration in the olfactory bulb |
Q45875394 | Patients and animal models of CNGβ1-deficient retinitis pigmentosa support gene augmentation approach |
Q33725907 | Peripherin-2 and Rom-1 have opposing effects on rod outer segment targeting of retinitis pigmentosa-linked peripherin-2 mutants. |
Q52651346 | Peripherin-2 couples rhodopsin to the CNG channel in outer segments of rod photoreceptors. |
Q41661702 | Photopharmacological control of bipolar cells restores visual function in blind mice |
Q46189889 | Physiological roles of cGMP-gated channels: lessons from mouse models and human channelopathies. |
Q61805403 | Production and Application of Stable Isotope-Labeled Internal Standards for RNA Modification Analysis |
Q43003710 | Quantification of the sixth DNA base hydroxymethylcytosine in the brain |
Q38858959 | Quantitative LC-MS Provides No Evidence for m6 dA or m4 dC in the Genome of Mouse Embryonic Stem Cells and Tissues |
Q41546036 | Quick and reliable method for retina dissociation and separation of rod photoreceptor perikarya from adult mice. |
Q112720048 | Redirected nuclear glutamate dehydrogenase supplies Tet3 with α-ketoglutarate in neurons |
Q38804444 | Remote and reversible inhibition of neurons and circuits by small molecule induced potassium channel stabilization |
Q30497586 | Restoration of cone vision in the CNGA3-/- mouse model of congenital complete lack of cone photoreceptor function |
Q52666370 | Retinal Cyclic Nucleotide-Gated Channels: From Pathophysiology to Therapy. |
Q38330163 | Retinal gene delivery by adeno-associated virus (AAV) vectors: Strategies and applications |
Q52930035 | Retinitis pigmentosa: impact of different Pde6a point mutations on the disease phenotype. |
Q94466892 | Safety and Vision Outcomes of Subretinal Gene Therapy Targeting Cone Photoreceptors in Achromatopsia: A Nonrandomized Controlled Trial |
Q38846304 | Stem Cell-Derived Photoreceptor Transplants Differentially Integrate Into Mouse Models of Cone-Rod Dystrophy. |
Q33541908 | Structural and functional phenotyping in the cone-specific photoreceptor function loss 1 (cpfl1) mouse mutant - a model of cone dystrophies |
Q45871060 | Subretinal Injection for Gene Therapy Does Not Cause Clinically Significant Outer Nuclear Layer Thinning in Normal Primate Foveae |
Q54319918 | Superior Retinal Gene Transfer and Biodistribution Profile of Subretinal Versus Intravitreal Delivery of AAV8 in Nonhuman Primates. |
Q114560223 | Suppression of SARS‐CoV‐2 Replication with Stabilized and Click‐Chemistry Modified siRNAs |
Q48546020 | Synaptic plasticity in CNGA3(-/-) mice: cone bipolar cells react on the missing cone input and form ectopic synapses with rods. |
Q90238248 | Synthesis of galactosyl-queuosine and distribution of hypermodified Q-nucleosides in mouse tissues |
Q114123690 | Systematic Studies on Stabilization of AAV Vector Formulations by Lyophilization |
Q57376702 | TET3 Is Recruited by REST for Context-Specific Hydroxymethylation and Induction of Gene Expression |
Q45128222 | Tet oxidizes thymine to 5-hydroxymethyluracil in mouse embryonic stem cell DNA. |
Q104613083 | The cGMP-Dependent Protein Kinase 2 Contributes to Cone Photoreceptor Degeneration in the Cnga3-Deficient Mouse Model of Achromatopsia |
Q33828402 | The cGMP-dependent protein kinase II Is an inhibitory modulator of the hyperpolarization-activated HCN2 channel |
Q43158222 | The cyclic nucleotide-gated ion channel CNGA3 contributes to coolness-induced responses of Grueneberg ganglion neurons |
Q39611720 | The glutamic acid-rich protein is a gating inhibitor of cyclic nucleotide-gated channels. |
Q28586569 | The murine HCN3 gene encodes a hyperpolarization-activated cation channel with slow kinetics and unique response to cyclic nucleotides |
Q33529014 | The retinitis pigmentosa mutation c.3444+1G>A in CNGB1 results in skipping of exon 32 |
Q21089989 | Tissue distribution of 5-hydroxymethylcytosine and search for active demethylation intermediates |
Q40036396 | Up-regulation of hyperpolarization-activated cyclic nucleotide-gated channel 3 (HCN3) by specific interaction with K+ channel tetramerization domain-containing protein 3 (KCTD3). |
Q35693904 | Vitreal delivery of AAV vectored Cnga3 restores cone function in CNGA3-/-/Nrl-/- mice, an all-cone model of CNGA3 achromatopsia |
Q37165487 | cGMP accumulation causes photoreceptor degeneration in CNG channel deficiency: evidence of cGMP cytotoxicity independently of enhanced CNG channel function |
Q42996656 | cGMP-dependent cone photoreceptor degeneration in the cpfl1 mouse retina. |
Q35978243 | cGMP/Protein Kinase G Signaling Suppresses Inositol 1,4,5-Trisphosphate Receptor Phosphorylation and Promotes Endoplasmic Reticulum Stress in Photoreceptors of Cyclic Nucleotide-gated Channel-deficient Mice |
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