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Top Articles

#TitleJournalYearCitations
1Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)Autophagy20164,701
2A mutation in the tRNALeu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathiesNature19901,981
3Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1Autophagy20211,430
4Adiponectin and AdipoR1 regulate PGC-1α and mitochondria by Ca2+ and AMPK/SIRT1Nature2010859
53-Mercaptopyruvate Sulfurtransferase Produces Hydrogen Sulfide and Bound Sulfane Sulfur in the BrainAntioxidants and Redox Signaling2009800
6Cells Respond to Mechanical Stress by Rapid Disassembly of CaveolaeCell2011791
7Brain hydrogen sulfide is severely decreased in Alzheimer's diseaseBiochemical and Biophysical Research Communications2002739
8Development of a Highly Selective Fluorescence Probe for Hydrogen SulfideJournal of the American Chemical Society2011614
9Fibrosis and adipogenesis originate from a common mesenchymal progenitor in skeletal muscleJournal of Cell Science2011517
10Skeletal Muscle FOXO1 (FKHR) Transgenic Mice Have Less Skeletal Muscle Mass, Down-regulated Type I (Slow Twitch/Red Muscle) Fiber Genes, and Impaired Glycemic ControlJournal of Biological Chemistry2004488
11Chronic restraint stress causes anxiety- and depression-like behaviors, downregulates glucocorticoid receptor expression, and attenuates glutamate release induced by brain-derived neurotrophic factor in the prefrontal cortexProgress in Neuro-Psychopharmacology and Biological Psychiatry2012479
12Intragenic deletion in the gene encoding ubiquitin carboxy-terminal hydrolase in gad miceNature Genetics1999467
13BDNF function and intracellular signaling in neuronsHistology and Histopathology2010464
14Stargazin modulates AMPA receptor gating and trafficking by distinct domainsNature2005447
15A Source of Hydrogen Sulfide and a Mechanism of Its Release in the BrainAntioxidants and Redox Signaling2009444
16A mutation in the ceruloplasmin gene is associated with systemic hemosiderosis in humansNature Genetics1995442
17Chronic Stress Induces Impairment of Spatial Working Memory Because of Prefrontal Dopaminergic DysfunctionJournal of Neuroscience2000426
18Possible association of Bifidobacterium and Lactobacillus in the gut microbiota of patients with major depressive disorderJournal of Affective Disorders2016419
19Vascular Endothelium Expresses 3-Mercaptopyruvate Sulfurtransferase and Produces Hydrogen SulfideJournal of Biochemistry2009410
20Crosstalk between Glucocorticoid Receptor and Nutritional Sensor mTOR in Skeletal MuscleCell Metabolism2011410
21The small GTPase RalA targets filamin to induce filopodiaProceedings of the National Academy of Sciences of the United States of America1999407
22Molecular Signature of Quiescent Satellite Cells in Adult Skeletal MuscleStem Cells2007402
23The presence of free D-serine in rat brainFEBS Letters1992400
24Interleukin 6 signaling promotes anti-aquaporin 4 autoantibody production from plasmablasts in neuromyelitis opticaProceedings of the National Academy of Sciences of the United States of America2011383
25Generation of mice with mitochondrial dysfunction by introducing mouse mtDNA carrying a deletion into zygotesNature Genetics2000366
26Microglia–Müller Glia Cell Interactions Control Neurotrophic Factor Production during Light-Induced Retinal DegenerationJournal of Neuroscience2002362
27Efficacy of systemic morpholino exon‐skipping in duchenne dystrophy dogsAnnals of Neurology2009356
28Mutations in the integrin α7 gene cause congenital myopathyNature Genetics1998355
29Glutamate Transporter GLAST Is Expressed in the Radial Glia–Astrocyte Lineage of Developing Mouse Spinal CordJournal of Neuroscience1997352
30Identification of Rap1 as a Target for the Crk SH3 Domain-Binding Guanine Nucleotide-Releasing Factor C3GMolecular and Cellular Biology1995350
31Human PTRF mutations cause secondary deficiency of caveolins resulting in muscular dystrophy with generalized lipodystrophyJournal of Clinical Investigation2009350
32Nonsense-mediated mRNA decay modulates clinical outcome of genetic diseaseEuropean Journal of Human Genetics2006348
33Three-dimensional reconstruction of the membrane skeleton at the plasma membrane interface by electron tomographyJournal of Cell Biology2006343
34Consensus Paper: Cerebellar DevelopmentCerebellum2016337
35Endogenous d-Serine in Rat Brain: N-Methyl-d-Aspartate Receptor-Related Distribution and AgingJournal of Neurochemistry1993335
36Evidence of novel neuronal functions of dysbindin, a susceptibility gene for schizophreniaHuman Molecular Genetics2004334
37Ubiquitin carboxy-terminal hydrolase L1 binds to and stabilizes monoubiquitin in neuronHuman Molecular Genetics2003328
38Mitochondrial neurogastrointestinal encephalomyopathy: An autosomal recessive disorder due to thymidine phosphorylase mutationsAnnals of Neurology2000324
39Cardiac side population cells have a potential to migrate and differentiate into cardiomyocytes in vitro and in vivoJournal of Cell Biology2007308
40Mice lacking bombesin receptor subtype-3 develop metabolic defects and obesityNature1997295
41Functional Comparison of d‐Serine and Glycine in Rodents: The Effect on Cloned NMDA Receptors and the Extracellular ConcentrationJournal of Neurochemistry1995295
42Mutations ofARX are associated with striking pleiotropy and consistent genotype-phenotype correlationHuman Mutation2004293
43Hydrogen sulfide induces calcium waves in astrocytesFASEB Journal2004292
44Hydrogen Sulfide: From Brain to GutAntioxidants and Redox Signaling2010287
45A new mtDNA mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS)Biochimica Et Biophysica Acta - Molecular Basis of Disease1991280
46Safety and efficacy of satralizumab monotherapy in neuromyelitis optica spectrum disorder: a randomised, double-blind, multicentre, placebo-controlled phase 3 trialLancet Neurology, The2020278
47Signaling Molecules: Hydrogen Sulfide and PolysulfideAntioxidants and Redox Signaling2015272
48Noncoding CGG repeat expansions in neuronal intranuclear inclusion disease, oculopharyngodistal myopathy and an overlapping diseaseNature Genetics2019265
49Alpha-CaMKII deficiency causes immature dentate gyrus, a novel candidate endophenotype of psychiatric disordersMolecular Brain2008261
50Murine cystathionine γ-lyase: complete cDNA and genomic sequences, promoter activity, tissue distribution and developmental expressionBiochemical Journal2004257