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3‐4: Near‐eye Display with Curved Waveguide for Fashionable Form Factor.
- Published in:
- SID Symposium Digest of Technical Papers, 2024, v. 55, n. 1, p. 11, doi. 10.1002/sdtp.17437
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- Article
Early postnatal serotonin modulation prevents adult-stage deficits in Arid1b-deficient mice through synaptic transcriptional reprogramming.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-32748-5
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- Publication type:
- Article
Author Correction: SLC6A20 transporter: a novel regulator of brain glycine homeostasis and NMDAR function.
- Published in:
- 2024
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- Correction Notice
SLC6A20 transporter: a novel regulator of brain glycine homeostasis and NMDAR function.
- Published in:
- EMBO Molecular Medicine, 2021, v. 13, n. 2, p. 1, doi. 10.15252/emmm.202012632
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- Article
LAR-RPTP Clustering Is Modulated by Competitive Binding between Synaptic Adhesion Partners and Heparan Sulfate.
- Published in:
- Frontiers in Molecular Neuroscience, 2017, p. 1, doi. 10.3389/fnmol.2017.00327
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- Publication type:
- Article
Early correction of synaptic long-term depression improves abnormal anxiety-like behavior in adult GluN2B-C456Y-mutant mice.
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- PLoS Biology, 2020, v. 18, n. 4, p. 1, doi. 10.1371/journal.pbio.3000717
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- Publication type:
- Article
Crystal structure analysis of c4763, a uropathogenic Escherichia coli-specific protein.
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- Acta Crystallographica: Section F, Structural Biology Communications, 2015, v. 71, n. 8, p. 1042, doi. 10.1107/S2053230X15013035
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- Article
Sequence preference and structural heterogeneity of BZ junctions.
- Published in:
- Nucleic Acids Research, 2018, v. 46, n. 19, p. 10504, doi. 10.1093/nar/gky784
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- Publication type:
- Article
Distinct Z-DNA binding mode of a PKR-like protein kinase containing a Z-DNA binding domain (PKZ).
- Published in:
- Nucleic Acids Research, 2014, v. 42, n. 9, p. 5937, doi. 10.1093/nar/gku189
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- Publication type:
- Article
Base extrusion is found at helical junctions between right- and left-handed forms of DNA and RNA.
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- Nucleic Acids Research, 2009, v. 37, n. 13, p. 4353, doi. 10.1093/nar/gkp364
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- Publication type:
- Article
A TBR1-K228E Mutation Induces Tbr1 Upregulation, Altered Cortical Distribution of Interneurons, Increased Inhibitory Synaptic Transmission, and Autistic-Like Behavioral Deficits in Mice.
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- Frontiers in Molecular Neuroscience, 2019, p. 1, doi. 10.3389/fnmol.2019.00241
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- Publication type:
- Article
Shank3 Mice Carrying the Human Q321R Mutation Display Enhanced Self-Grooming, Abnormal Electroencephalogram Patterns, and Suppressed Neuronal Excitability and Seizure Susceptibility.
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- Frontiers in Molecular Neuroscience, 2019, p. N.PAG, doi. 10.3389/fnmol.2019.00155
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- Publication type:
- Article
Scn2a Haploinsufficiency in Mice Suppresses Hippocampal Neuronal Excitability, Excitatory Synaptic Drive, and Long-Term Potentiation, and Spatial Learning and Memory.
- Published in:
- Frontiers in Molecular Neuroscience, 2019, p. N.PAG, doi. 10.3389/fnmol.2019.00145
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- Publication type:
- Article
SALM5 trans-synaptically interacts with LAR-RPTPs in a splicing-dependent manner to regulate synapse development.
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- Scientific Reports, 2016, p. 26676, doi. 10.1038/srep26676
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- Publication type:
- Article
Clinical Significance of Combining Preoperative and Postoperative Albumin-Bilirubin Score in Colorectal Cancer.
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- Cancer Research & Treatment, 2023, v. 55, n. 4, p. 1261, doi. 10.4143/crt.2022.1444
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- Publication type:
- Article
The lipoprotein-associated phospholipase A2 inhibitor Darapladib sensitises cancer cells to ferroptosis by remodelling lipid metabolism.
- Published in:
- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-41462-9
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- Publication type:
- Article
Distinct Rayleigh Scattering from Hot Spot Mutant p53 Proteins Reveals Cancer Cells.
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- Small, 2014, v. 10, n. 14, p. 2954, doi. 10.1002/smll.201400004
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- Publication type:
- Article
Protein interactome and cell‐type expression analyses reveal that cytoplasmic FMR1‐interacting protein 1 (CYFIP1), but not CYFIP2, associates with astrocytic focal adhesion.
- Published in:
- Journal of Neurochemistry, 2022, v. 162, n. 2, p. 190, doi. 10.1111/jnc.15622
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- Publication type:
- Article
Dominant transmission of de novo KIF1A motor domain variant underlying pure spastic paraplegia.
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- European Journal of Human Genetics, 2015, v. 23, n. 10, p. 1427, doi. 10.1038/ejhg.2014.297
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- Publication type:
- Article
Segmentation of Marine Forecast Zone in Korea by Using Wave Data: Based on K-Means Clustering Algorithm.
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- Journal of Coastal Research, 2021, v. 114, n. 1, p. 251, doi. 10.2112/JCR-SI114-051.1
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- Publication type:
- Article
SALM4 suppresses excitatory synapse development by cis-inhibiting trans-synaptic SALM3-LAR adhesion.
- Published in:
- Nature Communications, 2016, v. 7, n. 8, p. 12328, doi. 10.1038/ncomms12328
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- Publication type:
- Article
Structural basis for LAR-RPTP/Slitrk complex-mediated synaptic adhesion.
- Published in:
- Nature Communications, 2014, v. 5, n. 11, p. 5423, doi. 10.1038/ncomms6423
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- Publication type:
- Article
Reduced CYFIP2 Stability by Arg87 Variants Causing Human Neurological Disorders.
- Published in:
- 2019
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- Publication type:
- Letter
A novel de novo heterozygous DYRK1A mutation causes complete loss of DYRK1A function and developmental delay.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-66750-y
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- Publication type:
- Article
ENDOSCOPIC ENDONASAL OPTIC NERVE DECOMPRESSION FOR NONTRAUMATIC OPTIC NEUROPATHY: REPORT OF 3 CASES.
- Published in:
- Rhinology Supplement, 2018, v. 56, p. 605
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- Publication type:
- Article
Structural and functional studies of a large winged Z- DNA-binding domain of Danio rerio protein kinase PKZ.
- Published in:
- FEBS Letters, 2016, v. 590, n. 14, p. 2275, doi. 10.1002/1873-3468.12238
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- Publication type:
- Article
Lrfn2-Mutant Mice Display Suppressed Synaptic Plasticity and Inhibitory Synapse Development and Abnormal Social Communication and Startle Response.
- Published in:
- Journal of Neuroscience, 2018, v. 38, n. 26, p. 5872, doi. 10.1523/JNEUROSCI.3321-17.2018
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- Publication type:
- Article
De Novo Mutations in the Motor Domain of KIF1A Cause Cognitive Impairment, Spastic Paraparesis, Axonal Neuropathy, and Cerebellar Atrophy.
- Published in:
- Human Mutation, 2015, v. 36, n. 1, p. 69, doi. 10.1002/humu.22709
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- Publication type:
- Article