Negative immunostaining of Duchenne muscular dystrophy(DMD) and mdx muscle surface membrane with antibody against synthetic peptide fragment predicted from DMD cDNA.

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Progress in muscular dystrophy research with special emphasis on gene therapy
Histochemical Responses of Human Soleus Muscle Fibers to Long-Term Bedrest with or without Countermeasures
Dysferlinopathy associated with rigid spine syndrome
A carrier of Duchenne muscular dystrophy with dilated cardiomyopathy but no skeletal muscle symptom
Nationwide Survey of Neurologic Manifestations of Acquired Immunodeficiency Syndrome in Japan
Optimal Conditions for the Enzymatic Production of L-Aromatic Amino Acids from the Corresponding 5-Substituted Hydantoins(Microbiology & Fermentation Industry)
Optimal Conditions for the Enzymatic Production of D-Amino Acids from the Corresponding 5-Substituted Hydantoins(Microbiology & Fermentation Industry)
Enzymatic Production of L-Tryptophan from DL-5-Indolylmethylhydantoin by Mutants of Flavobacterium sp. T-523(Microbiology & Fermentation Industry)
Screening of Microorganisms Producing D-p-Hydroxyphenyl-glycine from DL-5-(p-Hydroxyphenyl)hydantoin(Microbiology & Fermentation Industry)
Siblings of Schwartz-Jampel Syndrome with abnormal muscle computed tomographic findings
A double mutation (G11778A and G12192A) in mitochondrial DNA associated with Leber's hereditary optic neuropathy and cardiomyopathy
Effects of Chronic Hindlimb Suspension on Landing Performance in Response to Head-Down Drop in Rats
Regulation of the Properties of Rat Hind Limb Muscles Following Gravitational Unloading
Asymmetric Synthesis of S-Carboxymethyl-L-cysteine by a Chemico-enzymatic Method (Microbiological & Fermentation Industry)
Expression of Myoferlin in Skeletal Muscles of Patients with Dysferlinopathy
Cardiac ankyrin repeat protein is preferentially induced in atrophic myofibers of congenital myopathy and spinal muscular atrophy
Canine X-Linked Muscular Dystophy in Japan(CXMD_)
Genetic Heterozygous Carriers in Hereditary Muscular Dystrophy of Chickens
Benign infantile neurogenic muscle atrophy predominantly involving the upper extremities
Fermentative Production of L-Glutamic-γ-Semialdehyde and Its Chemical Conversion into L-Tryptophan(Microbiology & Fermentation Industry)
Laminin in Animal Models for Muscular Dystrophy Defect of Laminin M in Skeletal and Cardiac Muscles and Peripheral Nerve of the Homozygous Dystrophic dy/dy Mice
Molecular diagnosis of muscular dystrophies
Cardiac Muscle Involvement in muscle Disorders
Oculopharyngeal Muscular Dystrophy Associated with Dementia
Regulation of phosphorylase kinase by low concentrations of Ca ions upon muscle contraction: the connection between metabolism and muscle contraction and the connection between muscle physiology and Ca-dependent signal transduction
Autosomal dominant Late-onset Quadriceps Myopathy: Three Patients of a Taiwanese Kindred
Porcine Skeletal Muscle Dystrophin
A monoclonal antibody against a synthetic polypeptide fragment of dystrophin (amino acid sequence from position 215 to 264).
Immunostaining of Dystrophin and Utrophin in Skeletal Muscle of Dystrophinopathies.
Anti-filamin and -vinculin antibodies in sera from patients with myasthenia gravis and polymyositis.
Negative immunostaining of Duchenne muscular dystrophy(DMD) and mdx muscle surface membrane with antibody against synthetic peptide fragment predicted from DMD cDNA.
Distal Myopathy in Multi-minicore Disease
A Dystrophin Homologue on the Surface Membrane of Embryonic and Denervated mdx Mouse Muscle Fibers.
Expression of a dystrophin-like protein on the surface membrane of muscle cells in mdx mice.
Studies on Cyclic Dipeptides. II. Isomerization among cyclo(-4-Hydroxyprolyl-4-hydroxyprolyl-)s and a Novel Conversion of D-allo-Hydroxyproline to L-Hydroxyproline
Human skeletal muscle contains two major aminopeptidases: An anion-activated aminopeptidase B and an aminopeptidase M-like enzyme.

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