يعرض 1 - 10 نتائج من 10 نتيجة بحث عن '"Apoptosis Inducing Factor: genetics"', وقت الاستعلام: 1.00s تنقيح النتائج
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    المساهمون: CNR Istituto di Biologia e Patologia Molecolari Roma (CNR, National Research Council of Italy, Apoptose, cancer et immunité (U848), Université Paris-Sud - Paris 11 (UP11)-Institut Gustave Roussy (IGR)-Institut National de la Santé et de la Recherche Médicale (INSERM), Institut Gustave Roussy (IGR), Université Paris-Sud - Paris 11 (UP11), This work has been partially supported by grants from the European Union (Apo-Sys) to G.K., and by MiUR of Italy (FIRB RBRN07BMCT “Italian Human Proteome Network”) to M.B. T.M. was recipient of a fellowship supported by MiUR of Italy (FIRB RBIN04PWNC)., We thank Gerry Melino (Rome, Italy) for helpful discussions and critical reading of the manuscript.

    المصدر: ISSN: 0006-291X.

    العلاقة: info:eu-repo/semantics/altIdentifier/pmid/19782043; hal-02356576; https://hal.science/hal-02356576Test; PUBMED: 19782043

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    المساهمون: D., Ghezzi, I., Sevrioukova, F., Invernizzi, C., Lamperti, M., Mora, D'Adamo, ADAMO PIO, F., Novara, O., Zuffardi, G., Uziel, M., Zeviani

    المصدر: The American Journal of Human Genetics. (4):639-649

    مصطلحات موضوعية: Mitochondrial encephalomyopathy, Male, DNA Primer, Riboflavin, Respiratory chain, Poly (ADP-Ribose) Polymerase-1, Apoptosis, Gene, drug effect [Skeletal], Apoptosis Inducing Factor, Apoptosis Inducing Factor: genetics, Apoptosis Inducing Factor: metabolism, Caspase 3, Caspase 3: metabolism, Computer Simulation, DNA, DNA Primers, DNA Primers: chemistry, Dietary Supplements, Electron Transport, Electron Transport: physiology, Female, Fibroblasts, Fibroblasts: cytology, Fibroblasts: drug effects, Fibroblasts: metabolism, Flavin-Adenine Dinucleotide, Flavin-Adenine Dinucleotide: metabolism, Genes, Humans, In Situ Nick-End Labeling, Infant, Magnetic Resonance Imaging, Mitochondrial, Mitochondrial Encephalomyopathies, Mitochondrial Encephalomyopathies: genetics, Mitochondrial Encephalomyopathies: metabolism, Mitochondrial Encephalomyopathies: pathology, Mitochondrial: genetics, Mitochondrial: metabolism, Monozygotic, Muscle, Mutation, Mutation: genetics, Nervous System Diseases, Nervous System Diseases: drug therapy, Nervous System Diseases: etiology, Newborn, Pedigree, Poly(ADP-ribose) Polymerases, Poly(ADP-ribose) Polymerases: metabolism, Protein Conformation, Riboflavin: administration \& dosage, Skeletal, Skeletal: cytology, Skeletal: drug effects, Skeletal: metabolism, Staurosporine, Staurosporine: pharmacology, Twins, X-Linked, Genes, X-Linked, Genetics(clinical), genetic [Mitochondrial], Poly(ADP-ribose) Polymerase, metabolism [Poly(ADP-ribose) Polymerases], chemistry [DNA Primers], Apoptosis-inducing factor, pathology [Mitochondrial Encephalomyopathies], metabolism [Fibroblasts], Human, DNA, Mitochondrial, genetic [Mutation], Genetics, metabolism [Caspase 3], Dietary Supplement, metabolism [Mitochondrial], Apoptosi, medicine.disease, metabolism [Skeletal], Monozygotic twin, drug effect [Fibroblasts], Mitochondrion, Mitochondrial Encephalomyopathie, Mitochondrial myopathy, cytology [Fibroblasts], Nervous System Disease, Genetics (clinical), cytology [Skeletal], metabolism [Mitochondrial Encephalomyopathies], physiology [Electron Transport], Biochemistry, metabolism [Flavin-Adenine Dinucleotide], Fibroblast, genetic [Mitochondrial Encephalomyopathies], AIFM1, Infant, Newborn, Muscle, Skeletal, Twins, Monozygotic, Biology, genetic [Apoptosis Inducing Factor], etiology [Nervous System Diseases], Severe X-linked mitochondrial encephalomyopathy, Report, pharmacology [Staurosporine], medicine, Twin, Molecular biology, metabolism [Apoptosis Inducing Factor], drug therapy [Nervous System Diseases], administration \& dosage [Riboflavin]

    وصف الملف: STAMPA