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Journal of the American Chemical Society, ISSN 0002-7863, 04/2014, Volume 136, Issue 13, pp. 5039 - 5046
The development of a stable, functional electrolyte is urgently required for fast-charging and high-voltage lithium-ion batteries as well as next-generation... 
CELLS | LI-ION | MOLECULAR-DYNAMICS | SURFACE-FILM FORMATION | XPS | CAPABILITY | INTERCALATION | CHEMISTRY, MULTIDISCIPLINARY | SPACE GAUSSIAN PSEUDOPOTENTIALS | GRAPHITE ELECTRODE | CHALLENGES | Lithium cells | Research | Properties | Acetonitrile
Journal Article
Journal Article
Pediatrics International, ISSN 1328-8067, 06/2016, Volume 58, Issue 6, pp. 445 - 449
Journal Article
ACS Applied Materials and Interfaces, ISSN 1944-8244, 07/2014, Volume 6, Issue 14, pp. 10892 - 10899
Lithium-ion batteries have exclusively employed an ethylene carbonate (EC)-based electrolyte to ensure the reversibility of the graphite negative electrode... 
concentrated solution | negative electrode | lithium-ion batteries | graphite | surface film | electrolyte | PROPYLENE CARBONATE | MATERIALS SCIENCE, MULTIDISCIPLINARY | SURFACE-FILM FORMATION | NANOSCIENCE & NANOTECHNOLOGY | SOLVATION | LI-ION BATTERIES | CHALLENGES | SOLVENTS | SYSTEMS | DIMETHYL-SULFOXIDE | ASSOCIATION | ELECTROCHEMICAL INTERCALATION
Journal Article
Journal Article
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 04/2019, Volume 126, Issue 4, pp. 362 - 367
Galactosemia is a metabolic disorder that affects the appropriate metabolism of β-D-galactose. Deficiencies in three of the enzymes of the Leloir pathway,... 
Genetics | Leloir pathway | GALM | Galactose | Galactose mutarotase
Journal Article
Genetics in Medicine, ISSN 1098-3600, 2018, Volume 21, Issue 6, pp. 1286 - 1294
Galactosemia is caused by metabolic disturbances at various stages of galactose metabolism, including deficiencies in enzymes involved in the Leloir pathway... 
galactose mutarotase | Leloir pathway | galactose | GALM | genetics
Journal Article
Journal Article
Annals of Neurology, ISSN 0364-5134, 06/2019, Volume 85, Issue 6, pp. 927 - 933
c‐Jun‐amino‐terminal kinase‐interacting protein 3 (JIP3), encoded by MAPK8IP3 , is an adaptor protein of the kinesin‐1 complex and essential for axonal... 
JIP3 | AXONAL-TRANSPORT | MUTATIONS | RILP | NEUROSCIENCES | CLINICAL NEUROLOGY | Hypoplasia | Phenotypes | Zebrafish | Kinases | Neurodevelopmental disorders | Embryos | Corpus callosum | Proteins | Atrophy | Axons | Lateral line | Coding | Axonal transport | Kinesin
Journal Article
FEBS Journal, ISSN 1742-464X, 03/2017, Volume 284, Issue 5, p. 766
  The preparation of a glycosynthase, a catalytic nucleophile mutant of a glycosidase, is a well-established strategy for the effective synthesis of glycosidic... 
Enzymes | Biological products | Analysis | Crystals | Hydrolases | Enzyme kinetics | Structure | Ligands | Biosynthesis | Fluorides | Mutation
Journal Article
Journal of Clinical Immunology, ISSN 0271-9142, 1/2017, Volume 37, Issue 1, pp. 67 - 79
Pediatric inflammatory bowel disease (IBD) is a heterogeneous disorder caused by multiple factors. Although genetic and immunological analyses are required for... 
targeted sequencing | Medical Microbiology | Biomedicine | Immunology | Very early-onset inflammatory bowel disease | primary immunodeficiency | Infectious Diseases | Internal Medicine | pediatric gastroenterology | ONSET IBD | X-LINKED INHIBITOR | CROHNS-DISEASE | VARIANTS | CHRONIC GRANULOMATOUS-DISEASE | INTERLEUKIN-10 RECEPTOR | IMMUNOLOGY | HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS | INFLAMMATORY-BOWEL-DISEASE | XIAP DEFICIENCY | MUTATIONS | X-Linked Inhibitor of Apoptosis Protein - deficiency | Humans | Inflammatory Bowel Diseases - immunology | Inflammatory Bowel Diseases - diagnosis | Child, Preschool | Male | Inflammatory Bowel Diseases - metabolism | Interleukin-10 Receptor alpha Subunit - deficiency | Inheritance Patterns | DNA Mutational Analysis | Inflammatory Bowel Diseases - genetics | Interleukin-10 Receptor alpha Subunit - metabolism | Interleukin-10 - metabolism | Female | Immunologic Deficiency Syndromes - immunology | Child | Cytokines - genetics | Cytokines - blood | Genetic Predisposition to Disease | Cytokines - metabolism | Genetic Association Studies | Signal Transduction | Japan | Genotype | X-Linked Inhibitor of Apoptosis Protein - genetics | Whole Exome Sequencing | Phenotype | Interleukin-10 Receptor alpha Subunit - genetics | Interleukin-10 - genetics | Adolescent | Alleles | X-Linked Inhibitor of Apoptosis Protein - metabolism | Immunologic Deficiency Syndromes - genetics | High-Throughput Nucleotide Sequencing | Mutation | Immunity - genetics | Pediatrics | Cytochrome b | Interleukins | Analysis | Gastrointestinal diseases | Genes | Immunodeficiency | Genetic research | Transplantation | Children | Health aspects | Hematopoietic stem cells | Index Medicus
Journal Article
Brain and Development, ISSN 0387-7604, 01/2019, Volume 41, Issue 1, pp. 122 - 122
Journal Article