Thermal instability of compound variants of carnitine palmitoyltransferase II and impaired mitochondrial fuel utilization in influenza-associated encephalopathy. - Wikidata - wikimedia - TriplyDB

Thermal instability of compound variants of carnitine palmitoyltransferase II and impaired mitochondrial fuel utilization in influenza-associated encephalopathy.

Thermal instability of compound variants of carnitine palmitoyltransferase II and impaired mitochondrial fuel utilization in influenza-associated encephalopathy.

http://www.wikidata.org/entity/Q40425971

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Nonalcoholic Lipid Accumulation and Hepatocyte Malignant Transformation Influenza virus pathogenicity regulated by host cellular proteases, cytokines and metabolites, and its therapeutic options Abbreviated half-lives and impaired fuel utilization in carnitine palmitoyltransferase II variant fibroblasts Host genetic determinants of influenza pathogenicity.Influenza-associated neurological complications.Diisopropylamine dichloroacetate, a novel pyruvate dehydrogenase kinase 4 inhibitor, as a potential therapeutic agent for metabolic disorders and multiorgan failure in severe influenza Influenza A virus infection of vascular endothelial cells induces GSK-3β-mediated β-catenin degradation in adherens junctions, with a resultant increase in membrane permeability.Increased missense mutation burden of Fatty Acid metabolism related genes in nunavik inuit population.Host genetics of severe influenza: from mouse Mx1 to human IRF7 Heat stroke with bimodal rhabdomyolysis: a case report and review of the literature Post-marketing assessment of neuropsychiatric adverse events in influenza patients treated with oseltamivir: an updated review.Influenza encephalopathy and related neuropsychiatric syndromes.A review of the indirect protection of younger children and the elderly through a mass influenza vaccination program in Japan.Diagnostic pitfall in antenatal manifestations of CPT II deficiency.Human Genetic Determinants of Viral Diseases.Up-regulation of ectopic trypsins in the myocardium by influenza A virus infection triggers acute myocarditis.Fatal viral infection-associated encephalopathy in two Chinese boys: a genetically determined risk factor of thermolabile carnitine palmitoyltransferase II variants.Carnitine palmitoyl transferase 2 polymorphism may be associated with enterovirus 71 severe infection in a Chinese population.A newborn case with carnitine palmitoyltransferase II deficiency initially judged as unaffected by acylcarnitine analysis soon after birth Mitochondrial carnitine palmitoyl transferase-II inactivity aggravates lipid accumulation in rat hepatocarcinogenesis.Penetration of oseltamivir and its active metabolite into the brain after lipopolysaccharide-induced inflammation in mice.

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P2860

Thermal instability of compound variants of carnitine palmitoyltransferase II and impaired mitochondrial fuel utilization in influenza-associated encephalopathy.

http://www.wikidata.org/entity/Q40425971

description

2008 nî lūn-bûn

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2008年の論文

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2008年学术文章

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2008年学术文章

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2008年学术文章

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2008年学术文章

@zh-my

2008年学术文章

@zh-sg

2008年學術文章

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2008年學術文章

@zh

2008年學術文章

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name

Thermal instability of compoun ...... nza-associated encephalopathy.

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type

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Thermal instability of compoun ...... nza-associated encephalopathy.

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Thermal instability of compoun ...... nza-associated encephalopathy.

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Thermal instability of compoun ...... nza-associated encephalopathy.

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P2093

Dengbing Yao

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Hiroshi Kido

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Hiroshi Mizuguchi

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Hiroshi Yamada

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Junji Chida

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Koji Shikata

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Miyoko Yamaguchi

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P2860

Mitochondrial fission and fusion mediators, hFis1 and OPA1, modulate cellular senescence

Observations on the affinity for carnitine, and malonyl-CoA sensitivity, of carnitine palmitoyltransferase I in animal and human tissues. Demonstration of the presence of malonyl-CoA in non-hepatic tissues of the rat

Molecular characterization of inherited carnitine palmitoyltransferase II deficiency

Thromboembolic disease due to thermolabile conformational changes of antithrombin Rouen-VI (187 Asn-->Asp)

Cleavage of structural proteins during the assembly of the head of bacteriophage T4

Carnitine palmitoyltransferase II deficiency: structure of the gene and characterization of two novel disease-causing mutations

Carnitine palmitoyltransferase deficiencies

Muscle carnitine palmityltransferase deficiency and myoglobinuria

Molecular mechanism of a temperature-sensitive phenotype in peroxisomal biogenesis disorder

Identification of 16 new disease-causing mutations in the CPT2 gene resulting in carnitine palmitoyltransferase II deficiency

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718-727

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scholarly article

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10.1002/HUMU.20717

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5

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29

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2008-05-01T00:00:00Z

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18306170

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