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APP as a Protective Factor in Acute Neuronal Insults.
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- Frontiers in Molecular Neuroscience, 2017, v. 10, p. 1, doi. 10.3389/fnmol.2017.00022
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- Publication type:
- Article
Contribution of N- and C-terminal channel domains to Kv channel interacting proteins in a mammalian cell line.
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- Journal of Physiology, 2005, v. 568, n. 2, p. 397, doi. 10.1113/jphysiol.2005.094359
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- Article
Phosphorylated guanidinoacetate partly compensates for the lack of phosphocreatine in skeletal muscle of mice lacking guanidinoacetate methyltransferase.
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- Journal of Physiology, 2004, v. 560, n. 1, p. 219, doi. 10.1113/jphysiol.2004.067926
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- Article
Autophagy regulates neuronal excitability by controlling cAMP/protein kinase A signaling at the synapse.
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- EMBO Journal, 2022, v. 41, n. 22, p. 1, doi. 10.15252/embj.2022110963
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- Article
Identification and functional characterization of a novel KCNE2 (MiRP1) mutation that alters HERG channel kinetics.
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- Journal of Molecular Medicine, 2002, v. 80, n. 8, p. 524, doi. 10.1007/s00109-002-0364-0
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- Article
A novel long-QT 5 gene mutation in the C-terminus (V109I) is associated with a mild phenotype.
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- Journal of Molecular Medicine, 2001, v. 79, n. 9, p. 504, doi. 10.1007/s001090100249
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- Publication type:
- Article
A novel long-QT 5 gene mutation in the C-terminus (V109I) is associated with a mild phenotype.
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- Journal of Molecular Medicine, 2001, v. 79, n. 9, p. 547, doi. 10.1007/s001090100280
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- Publication type:
- Article
Transcriptomic and metabolic analyses reveal salvage pathways in creatine-deficient AGAT mice.
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- Amino Acids, 2016, v. 48, n. 8, p. 2025, doi. 10.1007/s00726-016-2202-7
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- Publication type:
- Article
Homoarginine supplementation improves blood glucose in diet-induced obese mice.
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- Amino Acids, 2015, v. 47, n. 9, p. 1921, doi. 10.1007/s00726-015-2022-1
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- Article
Impaired cardiac contractile function in arginine:glycine amidinotransferase knockout mice devoid of creatine is rescued by homoarginine but not creatine.
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- Cardiovascular Research, 2018, v. 114, n. 3, p. 417, doi. 10.1093/cvr/cvx242
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- Article
Creatine, guanidinoacetate and homoarginine in statin-induced myopathy.
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- 2020
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- Publication type:
- Letter
Muscle phenotype of AGAT- and GAMT-deficient mice after simvastatin exposure.
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- Amino Acids, 2020, v. 52, n. 1, p. 73, doi. 10.1007/s00726-019-02812-4
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- Publication type:
- Article
Differential regulation of AMPK activation in leptin- and creatine-deficient mice.
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- FASEB Journal, 2013, v. 27, n. 10, p. 4147, doi. 10.1096/fj.12-225136
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- Publication type:
- Article
Cardiac arrhythmia induced by genetic silencing of 'funny' (f) channels is rescued by GIRK4 inactivation.
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- Nature Communications, 2014, v. 5, n. 8, p. 4664, doi. 10.1038/ncomms5664
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- Article
Seizures, behavioral deficits, and adverse drug responses in two new genetic mouse models of HCN1 epileptic encephalopathy.
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- eLife, 2022, p. 1, doi. 10.7554/eLife.70826
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- Publication type:
- Article
GABAergic Transmission during Brain Development: Multiple Effects at Multiple Stages.
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- Neuroscientist, 2018, v. 24, n. 1, p. 36, doi. 10.1177/1073858417701382
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- Article
Inhibition of G protein-gated K+ channels by tertiapin-Q rescues sinus node dysfunction and atrioventricular conduction in mouse models of primary bradycardia.
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- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-66673-8
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- Article
L-arginine:glycine amidinotransferase deficiency protects from metabolic syndrome.
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- Human Molecular Genetics, 2013, v. 22, n. 19, p. 4030, doi. 10.1093/hmg/ddt320
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- Publication type:
- Article
l-arginine:glycine amidinotransferase deficiency protects from metabolic syndrome.
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- Human Molecular Genetics, 2013, v. 22, n. 1, p. 110, doi. 10.1093/hmg/dds407
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- Publication type:
- Article
The Na<sup>+</sup>/H<sup>+</sup> Exchanger Nhe1 Modulates Network Excitability via GABA Release.
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- Cerebral Cortex, 2019, v. 29, n. 10, p. 4263, doi. 10.1093/cercor/bhy308
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- Article
Adenosine Receptor Antagonists Including Caffeine Alter Fetal Brain Development in Mice.
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- Science Translational Medicine, 2013, v. 5, n. 197, p. 1, doi. 10.1126/scitranslmed.3006258
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- Article
A mechanistic link between glia and neuronal excitability in acute neuroinflammation.
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- Journal of Physiology, 2017, v. 595, n. 3, p. 603, doi. 10.1113/JP273252
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- Publication type:
- Article
Conditional transgenic suppression of M channels in mouse brain reveals functions in neuronal excitability, resonance and behavior.
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- Nature Neuroscience, 2005, v. 8, n. 1, p. 51, doi. 10.1038/nn1375
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- Article
Dentate Gyrus Sharp Waves, a Local Field Potential Correlate of Learning in the Dentate Gyrus of Mice.
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- Journal of Neuroscience, 2020, v. 40, n. 37, p. 7105, doi. 10.1523/jneurosci.2275-19.2020
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- Article
Disturbed Prefrontal Cortex Activity in the Absence of Schizophrenia-Like Behavioral Dysfunction in Arc/Arg3.1 Deficient Mice.
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- Journal of Neuroscience, 2019, v. 39, n. 41, p. 8149, doi. 10.1523/jneurosci.0623-19.2019
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- Article
In vivo cardiac <sup>1</sup>H-MRS in the mouse.
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- Magnetic Resonance in Medicine, 2004, v. 52, n. 5, p. 1029, doi. 10.1002/mrm.20257
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- Article
MR spectroscopy of muscle and brain in guanidinoacetate methyltransferase (GAMT)-deficient mice: Validation of an animal model to study creatine deficiency.
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- Magnetic Resonance in Medicine, 2003, v. 50, n. 5, p. 936, doi. 10.1002/mrm.10627
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- Article
A homozygous SCN5A mutation in a severe, recessive type of cardiac conduction disease.
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- Human Mutation, 2010, v. 31, n. 8, p. E1609, doi. 10.1002/humu.21302
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- Publication type:
- Article
C-terminal HERG (LQT2) mutations disrupt IKr channel regulation through 14-3-3ε.
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- Human Molecular Genetics, 2006, v. 15, n. 19, p. 2888, doi. 10.1093/hmg/ddl230
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- Article
Mutations in classical late infantile neuronal ceroid lipofuscinosis disrupt transport of tripeptidyl-peptidase I to lysosomes.
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- Human Molecular Genetics, 2004, v. 13, n. 20, p. 2483, doi. 10.1093/hmg/ddh264
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- Article
Severely altered guanidino compound levels, disturbed body weight homeostasis and impaired fertility in a mouse model of guanidinoacetate N-methyltransferase (GAMT) deficiency.
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- Human Molecular Genetics, 2004, v. 13, n. 9, p. 905, doi. 10.1093/hmg/ddh112
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- Article
Two novel frameshift mutations causing premature stop codons in a patient with the severe form of Maroteaux-Lamy syndrome.
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- Human Mutation, 1996, v. 7, n. 4, p. 361, doi. 10.1002/(SICI)1098-1004(1996)7:4<361::AID-HUMU12>3.0.CO;2-0
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- Article
A Mouse Model of Creatine Transporter Deficiency Reveals Impaired Motor Function and Muscle Energy Metabolism.
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- Frontiers in Physiology, 2018, p. 1, doi. 10.3389/fphys.2018.00773
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- Article
Postnatal Disruption of the Disintegrin/Metalloproteinase ADAM 10 in Brain Causes Epileptic Seizures, Learning Deficits, Altered Spine Morphology, and Defective Synaptic Functions.
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- Journal of Neuroscience, 2013, v. 33, n. 32, p. 12915, doi. 10.1523/JNEUROSCI.5910-12.2013
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- Publication type:
- Article