Pages that link to "Q43904359"

The following pages link to Enzyme studies of skeletal muscle in mice with hereditary muscular dystrophy (Q43904359):

Displaying 27 items.

• Death in Embryonic Systems (Q28251799) (← links)
• Biochemical studies in dystrophic mouse muscle (Q36072200) (← links)
• The value of enzyme histochemical techniques in the classification of fibre types of human skeletal muscle. 3. Human skeletal muscles with inherited or acquired disease of the neuromuscular system (Q39824842) (← links)
• Enzymological studies on hereditary avian muscular dystrophy (Q39996045) (← links)
• STUDIES OF MYOSIN IN HEREDITARY MUSCULAR DYSTROPHY IN MICE. (Q40327285) (← links)
• Insulin secretion and carbohydrate metabolism in the dystrophic mouse (Q41005042) (← links)
• Enzyme alteration in skeletal muscle of mice with muscular dysthrophy (Q41346898) (← links)
• Histochemical observations in preclinical mouse muscular dystrophy (Q41956194) (← links)
• Effects of denervation on the activities of some tricarboxylic acid-cycle-associated dehydrogenases and adenine-metabolizing enzymes in rat diaphragm muscle (Q42154991) (← links)
• Protein degradation in skin fibroblasts from patients with Duchenne muscular dystrophy (Q42175801) (← links)
• Comparison of the protein-synthesizing machinery in the skeletal muscle of normal and dystrophic Bar Harbor mice (Q42274676) (← links)
• Adenosine 5′-triphosphate–creatine phosphotransferase from dystrophic mouse skeletal muscle. A genetic lesion associated with the catalytic-site thiol group (Q42588887) (← links)
• Electron-microscopic, cytochemical and biochemical studies of acetylcholinesterase and butyrylcholinesterase activity in muscle of dystrophic mice (Q45866020) (← links)
• [Muscle energy metabolism in children with progressive muscular dystrophy type Duchenne. Metabolites of the Embden-Meyerhof pathway, the citric acid cycle and high energy phosphates and enzyme activity of alpha-glycerol-oxidase, succinate-dehydrogen (Q54132665) (← links)
• Connective Tissue and the Pentose Phosphate Pathway in Normal and Denervated Muscle (Q59096689) (← links)
• Early changes in muscle glucose-6-phosphate dehydrogenase activity after denervation: Locus and dependence on nerve stump length (Q66956523) (← links)
• Biochemical and electrophoretic studies of cholinesterases in the muscular dysgenesis (mdg) mutant mouse (Q66977344) (← links)
• Creatine phosphokinase activity in dysgenic (mdg/mdg) mouse muscle (Q67039085) (← links)
• Noradrenaline metabolizing enzymes in normal and sympathetically denervated vas deferens (Q70555288) (← links)
• The inhibitory effect of actinomycin D and cycloheximide on the increase in activity of glucose-6-phosphate dehydrogenase and 6-phosphogluconate dehydrogenase in experimentally induced diseased skeletal muscles (Q70620387) (← links)
• Cholinesterase in muscle of dystrophic hamsters (Bio-40.54) (Q70737098) (← links)
• The increase in activity of glucose-6-phosphate dehydrogenase and 6-phosphogluconate dehydrogenase in skeletal muscles of rats after subcutaneous administration of N,N?-dimethyl-para-phenylenediamine (Q70874356) (← links)
• Glycolytic, Pentose‐Phosphate Shunt and Transaminase Enzymes in Gastrocnemius Muscle, Liver, Heart, and Brain of Two Mouse Mutants, 129 J‐dy and A2G‐adr, with Abnormal Muscle Function (Q70878297) (← links)
• Levels of protein and non-protein sulphydryl groups in the skeletal muscle of normal and dystrophic Bar Harbor mice (Q72248655) (← links)
• Accumulation of triose phosphates in dystrophic mouse muscle homogenates (Q72645013) (← links)
• Denervation modulated changes in mouse skeletal muscle RNA concentration (Q72666603) (← links)
• Oxidative stress as a potential pathogenic mechanism in an animal model of Duchenne muscular dystrophy (Q73778888) (← links)