Expression of ARPP-16/19 in Rat Denervated Skeletal Muscle
スポンサーリンク
概要
- 論文の詳細を見る
- Japanese Biochemical Societyの論文
- 2003-07-01
著者
-
Nishino Ichizo
国立精神･神経センター神経研究所 疾病研究第一部
-
Nishino Ichizo
Department Of Neuromuscular Research National Institute Of Neuroscience National Center Of Neurology
-
Nishino I
Department Of Neuromuscular Research National Institute Of Neuroscience National Center Of Neurology
-
HAYASHI Yukiko
Department of Neuromuscular Research, National Institute of Neuroscience, National Center of Neurolo
-
GOTO Yu-ichi
Department of Mental Retardation and Birth Defect Research, National Institute of Neuroscience, Nati
-
Hayashi Yukiko
Department Of Neuromuscular Research National Institute Of Neuroscience National Center Of Neurology
-
Yoshikawa Ayumu
Department of Pharmacology, Saitama Medical University
-
SASAGAWA Noboru
Department of Life Science, Graduate School of Arts and Science, The University of Tokyo
-
ISHIURA Shoichi
Department of Life Science, Graduate School of Arts and Science, The University of Tokyo
-
Goto Yu-ichi
Department Of Child Neurology National Center Hospital For Mental Nervous And Musculardisorders Nati
-
Yoshikawa Ayumu
Department Of Life Sciences Graduate School Of Arts And Sciences The University Of Tokyo
-
Sasagawa Noboru
Department Of Agricultural Chemistry The University Of Tokyo
-
Ishiura Shoichi
Department Of Life Sciences Graduate School Of Arts And Sciences University Of Tokyo
-
Ishiura Shoichi
Department Of Life And Cognitive Sciences College Of Arts And Sciences The University Of Tokyo
-
Ishiura Shoichi
Division Of Neuromuscular Research National Institute Of Neuroscience
-
Hayashi Yutaka
Life Science Research Center College Of Bioresource Sciences Nihon University
-
Nishino Ichizo
Department Of Neuromuscular Disorders National Institute Of Neuroscience National Center Of Neurolog
-
Ishiura S
Univ. Tokyo Tokyo Jpn
-
Ishiura S
Department Of Life Sciences Graduate School Of Arts And Sciences University Of Tokyo
-
MITSUHASHI Hiroaki
Department of Life Sciences, Graduate School of Arts and Sciences, The University of Tokyo
-
TSUKAHARA Toshifumi
Department of Neuromuscular Research, National Institute of Neuroscience, National Center of Neurolo
-
Tsukahara Toshifumi
Department Of Neuromuscular Research National Institute Of Neuroscience National Center Of Neurology
-
Hayashi Yukiko
Department Of Internal Medicine Asama General Hospital
-
Goto Yu-ichi
Department Of Mental Retardation And Birth Defect Research National Institute Of Neuroscience Nation
-
Mitsuhashi Hiroaki
Department Of Life Sciences Graduate School Of Arts And Sciences The University Of Tokyo
-
NISHINO Ichizo
Department of Neuromuscular Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry
関連論文
- A novel POMT2 mutation causes mild congenital muscular dystrophy with normal brain MRI
- Mutational Analysis of Fukutin Gene in Dilated Cardiomyopathy and Hypertrophic Cardiomyopathy(Molecular Cardiology)
- Genotype and phenotype analyses in 136 patients with single large-scale mitochondrial DNA deletions
- A novel FKRP gene mutation in a Taiwanese patient with limb-girdle muscular dystrophy 2I
- Characterization of lobulated fibers in limb girdle muscular dystrophy type 2A by gene expression profiling
- Subcellular Localization of Fukutin and Fukutin-Related Protein in Muscle Cells
- Localization of Calpain 3 in Human Skeletal Muscle and Its Alteration in Limb-Girdle Muscular Dystrophy 2A Muscle
- DPE-070 Initial Anti-Inflammatory Treatment with Cyclooxygenase-2 Inhibitor Protects Cardiac Dysfunction in a Blood Pressure Independent Manner(DPE12,Cardiomyopathy/Hypertrophy (Basic) (M),Digital Poster Session (English),The 73rd Annual Scientific Meetin
- A new clinicopathological entity of IgG4-related autoimmune disease
- Production of Anti-Amyloid β Antibodies in Mice Fed Rice Expressing Amyloid β
- PJ-442 Fukutin Gene Mutations Cause Dilated Cardiomyopathy with Minimal Muscle Weakness(Cardiomyopathy, basic/clinical-6, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
- Allelic Loss of 14q and 22q, NF2 Mutation, and Genetic Instability Occur Independently of c-kit Mutation in Gastrointestinal Stromal Tumor
- MEN1 gene mutations in sporadic neuroendocrine tumors of foregut derivation
- Polymerase chain reaction screening of immunoglobulin heavy chain and T cell receptor γ gene rearrangements: A practical approach to molecular DNA analysis of non-Hodgkin's lymphoma in a surgical pathology laboratory
- Pyothorax-associated lymphoma : Development of Epstein-Barr virus-associated lymphoma within the inflammatory cavity
- Intracranial meningioma masquerading as a primary pleuropulmonary tumor
- Coexpression of the CUG-Binding Protein Reduces DM Protein Kinase Expression in COS Cells
- Interaction between Emerin and Nuclear Lamins
- Overexpression, Purification, and Characterization of Human m-Calpain and Its Active Site Mutant, m-C105S-Calpain, Using a Baculovirus Expression System
- Expression and Antigenicity of Human Herpesvirus 8 Encoded ORF59 Protein in AIDS-Associated Kaposi's Sarcoma
- Dysferlinopathy associated with rigid spine syndrome
- Distal myopathy with rimmed vacuoles in a case of opercular syndrome
- Ecthyma gangrenosum combined with multiple perforations of the small intestine associated with Pseudomonas aeruginosa
- Novel LAMP-2 Mutation in a Family With Danon Disease Presenting With Hypertrophic Cardiomyopathy
- Early onset distal muscular dystrophy
- K-ras mutation in the major duodenal papilla and gastric and colonic mucosa in patients with autoimmune pancreatitis
- A carrier of Duchenne muscular dystrophy with dilated cardiomyopathy but no skeletal muscle symptom
- Treatment of mitochondrial encephalomyopathy with a combination of cytochrome C and vitamins B_1 and B_2
- Recurrent pain attacks in a 3-year-old patient with myoclonus epilepsy associated with ragged-red fibers(MERRF):a single-photon emission computed tomographic(SPECT)and electrophysiological study
- Long-term therapy with cytochrome c, flavin mononucleotide and thiamine diphosphate for a patient with Kearns-Sayre syndrome
- Construction and Some Characterization of a Yeast Artificial Chromosome Library from DNA of a Tomato Line Having Four Disease Resistance Traits
- Dystrophin gene analysis on 130 patients with Duchenne muscular dystrophy with a special reference to muscle mRNA analysis
- PJ-095 Relationship between (Pro)renin Receptor Shedding and its Intracellular Signaling(PJ016,Molecular Biology/Genetics, Myocardium, Vascular (M),Poster Session (Japanese),The 73rd Annual Scientific Meeting of The Japanese Circulation Society)
- Design of BACE1 Inhibitors : Replacing the P_1' Residue with Non-Acidic Moiety
- Design of β-Secretase (BACE1) Inhibitors with Carboxylic Acid Bioisosteres
- A Patient with mitochondrial myopathy associated with isolated succinate dehydrogenase deficiency
- Malignant hyperthermia susceptibility diagnosed with a family-specific ryanodine receptor gene type 1 mutation
- A double mutation (G11778A and G12192A) in mitochondrial DNA associated with Leber's hereditary optic neuropathy and cardiomyopathy
- Two pathogenic point mutations exist in the authentic mitochondrial genome, not in the nuclear pseudogene
- Mitochondrial DNA mutations in Leigh syndrome and their phylogenetic implications
- Design and Synthesis of β-Secretase Inhibitors Containing Hydroxymethylcarbonyl Isostere as a Transition State Mimic
- Early onset distal muscular dystrophy with normal dysferlin expression
- Aspergillus oryzae palB^ Encodes a Calpain-Like Protease : Homology to Emericella nidulans PalB and Conservation of Functional Regions
- A case of congenital neuromuscular disease with uniform type 1 fibers
- Limited Proteolysis of Filamin Is Catalyzed by Caspase-3 in U937 and Jurkat Cells^1
- Autolysis of Calpain Large Subunit Inducing Irreversible Dissociation of Stoichiometric Heterodimer of Calpain
- Thimet Oligopeptidase Cleaves the Full-Length Alzheimer Amyloid Precursor Protein at a β-Secretase Cleavage Site in COS Cells^1
- Deletion of an Endosomal/Lysosomal Targeting Signal Promotes the Secretion of Alzheimer's Disease Amyloid Precursor Protein (APP)
- Direct Evidence for Two Distinct Forms of the Flavoprotein Subunit of Human Mitochondrial Complex II (Succinate-Ubiquinone Reductase)
- Familial reducing body myopathy
- SAR study of BACE1 inhibitors containing pyridine derivatives
- Denervation Enhances the Expression of SHPS-1 in Rat Skeletal Muscle
- Expression of ARPP-16/19 in Rat Denervated Skeletal Muscle
- Enzymological Characterization of EpoA, a Laccase-Like Phenol Oxidase Produced by Streptomyces griseus
- Leigh syndrome caused by mitochondrial DNA G13513A mutation : frequency and clinical features in Japan
- IMMUNOHISTOCHEMICAL STUDY OF DYSTROPHIN IN DUCHENNE MUSCULAR DYSTROPHY
- The First Molecular Evidence That Autophagy Relates Rimmed Vacuole Formation in Chloroquine Myopathy
- Altered expression of CUG binding protein 1 mRNA in myotonic dystrophy 1 : possible RNA-RNA interaction
- Assessment of SMAD4, p53, and Ki-67 Alterations as a Predictor of Liver Metastasis in Human Colorectal Cancer
- Effects of a New Dihydropyridine Derivative, FRC-8653,on Blood Pressure in Conscious Spontaneously Hypertensive Rats
- Quantitative Analysis of CUG-BP1 Binding to RNA Repeats
- Identification and Characterization of the Hesr1/Hey1 as a Candidate trans-Acting Factor on Gene Expression through the 3' Non-Coding Polymorphic Region of the Human Dopamine Transporter (DAT1) Gene
- Overexpression of Human Myotonic Dystrophy Protein Kinase in Schizosaccharomyces pombe Induces an Abnormal Polarized and Swollen Cell Morphology
- Expression of Human ADAM9, ADAM10 and ADAM17 in COS-7 cells
- Suppression of Calcium-Induced Removal of the Z-Line by a Thiol-Protease Inhibitor,E-64-c
- Progressive myoclonus epilepsy with unusual neuropathologic features
- Function of ADAM9 in Xenopus Embryos
- PE-312 Clinical and Molecular Analyses of Nuclear Envelopathy(Cardiomyopathy, basic/clinical-5, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
- Humanin expression in skeletal muscles of patients with chronic progressive external ophthalmoplegia
- Intestinal pseudo-obstruction in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) associated with phenytoin therapy
- Abnormal glucose metabolism in aromatic L-amino acid decarboxylase deficiency
- Mitochondrial encephalomyopathy
- Bilateral occipital cortical dysplasia and white matter T2 hyperintensity with mild non-specific myopathy : Two sibling cases
- Study on a soluble splicing variant of human ADAM9
- Central nervous system and muscle involvement in an adolescent patient with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency
- Production of Anti-Amyloid β Antibodies in Mice Fed Rice Expressing Amyloid β
- Antiserum against the Synthetic Polypeptide Fragment of Dystrophin Cross-reacts with Myofibrillar C-protein
- Localization of BLT Serine Esterase is Distinct from that of Perforin in Cytotoxic T Lymphocyte
- The“ATP-Dependent Protease”in Human Erythroleukemia (K562) Cells is Identical to a High-Molecular-Mass Protease, Ingensin
- Molecular genetic analysis of dysferlin in Japanese patients with Miyoshi myopathy
- OJ-120 Clinical features of cardiac involvement in 51 patients with genetically-confirmed Danon disease(Cardiomyopathy, basic / clinical(02)(M),Oral Presentation (Japanese),The 72nd Annual Scientific Meeting of the Japanese Circulation Society)
- Functional analysis of ryanodine receptor type 1 p.R2508C mutation in exon 47
- Myopathy and neurogenic muscular atrophy in unexpected cardiopulmonary arrest
- Mitochondrial Encephalomyopathy Associated with Diabetes Mellitus, Cataract, and Corpus Callosum Atrophy
- Novel Mutations in the Gene Encoding Acid .ALPHA.-1,4-glucosidase in a Patient with Late-onset Glycogen Storage Disease Type II (Pompe Disease) with Impaired Intelligence
- Copy-number variations on the X chromosome in Japanese patients with mental retardation detected by array-based comparative genomic hybridization analysis
- Myotonic dystrophy type 2 is rare in the Japanese population
- Profiles of blood biomarkers in alternating hemiplegia of childhood-Increased MMP-9 and decreased substance P indicates its pathophysiology
- A Novel Mutation of the GAA Gene in a Patient with Adult-onset Pompe Disease Lacking a Disease-specific Pathology
- Staining of the nemaline rods by fluorescent antibody against Z-protein.
- Gel electrophoretic study of nemaline muscle.
- Coexpression of the CUG-Binding Protein Reduces DM Protein Kinase Expression in COS Cells.
- Limited Proteolysis of Filamin Is Catalyzed by Caspase-3 in U937 and Jurkat Cells.
- Expression of ARPP-16/19 in Rat Denervated Skeletal Muscle
- The First Molecular Evidence That Autophagy Relates Rimmed Vacuole Formation in Chloroquine Myopathy.
- Thimet Oligopeptidase Cleaves the Full-Length Alzheimer Amyloid Precursor Protein at a .BETA.-Secretase Cleavage Site in COS Cells.
- Identification of an Interleukin-1.BETA. Converting Enzyme-Like Activity That Increases upon Treatment of P19 Cells with Retinoic Acid as the Proteasome.
- Enzymological Characterization of EpoA, a Laccase-Like Phenol Oxidase Produced by Streptomyces griseus
- Overexpression of Human Myotonic Dystrophy Protein Kinase in Schizosaccharomyces pombe Induces an Abnormal Polarized and Swollen Cell Morphology
- Non-activated APJ suppresses the angiotensin II type 1 receptor, whereas apelin-activated APJ acts conversely