| review article | Q7318358 |
| scholarly article | Q13442814 |
| P356 | DOI | 10.1007/BF02337773 |
| P698 | PubMed publication ID | 1874604 |
| P50 | author | Giovanni Meola | Q42696154 |
| P2860 | cites work | The Duchenne muscular dystrophy gene product is localized in sarcolemma of human skeletal muscle | Q24297845 |
| Deletions of mitochondrial DNA in Kearns-Sayre syndrome | Q28297900 | ||
| X chromosome-linked muscular dystrophy (mdx) in the mouse | Q28589078 | ||
| Expression of a single transfected cDNA converts fibroblasts to myoblasts | Q29547764 | ||
| Satellite cell of skeletal muscle fibers | Q29615148 | ||
| Dystrophin: the protein product of the Duchenne muscular dystrophy locus | Q29618077 | ||
| Genetics of type II glycogenosis: Assignment of the human gene for acid α-glucosidase to chromosome 17 | Q33974862 | ||
| Defective myoblasts identified in Duchenne muscular dystrophy | Q34263737 | ||
| Human--rat muscle somatic cell hybrids form myotubes and express human muscle gene products | Q35464141 | ||
| Isolation and characterization of human muscle cells | Q36368262 | ||
| In vitro genetic transfer of protein synthesis and respiration defects to mitochondrial DNA-less cells with myopathy-patient mitochondria | Q36689236 | ||
| Transformation of human skeletal muscle cells by simian virus 40 | Q37549114 | ||
| Muscular carnitine synthesis and palmitate metabolism in vitro | Q39501840 | ||
| Diseased muscle cells in culture | Q39716157 | ||
| Reincarnation in cultured muscle of mitochondrial abnormalities. Two patients with epilepsy and lactic acidosis | Q40187619 | ||
| Characterization of glycogen phosphorylase isoenzymes present in cultured skeletal muscle from patients with McArdle's disease | Q40504492 | ||
| Expression of muscle-gene-specific isozymes of phosphorylase and creatine kinase in innervated cultured human muscle | Q41510849 | ||
| Differential expression of nuclear genes for cytochrome c oxidase during myogenesis | Q41738757 | ||
| Dystrophin is expressed in mdx skeletal muscle fibers after normal myoblast implantation | Q42102166 | ||
| A case of mitochondrial myopathy, lactic acidosis and complex I deficiency | Q43635325 | ||
| Generation of human myogenic cell lines by the transformation of primary culture with origin-defective SV40 DNA. | Q43966928 | ||
| Increased activity of calcium leak channels in myotubes of Duchenne human and mdx mouse origin | Q44177784 | ||
| Injection of mitochondria into human cells leads to a rapid replacement of the endogenous mitochondrial DNA. | Q44352356 | ||
| AMP deaminase: stage-specific isozymes in differentiating chick muscle | Q44607756 | ||
| Direct gene transfer into mouse muscle in vivo | Q44656494 | ||
| Mitochondrial myopathies: morphological and biochemical studies in human muscle cultures | Q44947421 | ||
| Heteroplasmy of mitochondrial genomes in clonal cultures from patients with Kearns-Sayre syndrome | Q45741572 | ||
| Differential expression of creatine kinase and phosphoglycerate mutase isozymes during development in aneural and innervated human muscle culture | Q45747866 | ||
| Increased protein degradation results from elevated free calcium levels found in muscle from mdx mice | Q46266620 | ||
| Muscle phosphoglycerate rnutase deficiency | Q48941160 | ||
| Histochemical Phosphorylase Activity in Regenerating Muscle Fibers from Myophosphorylase-Deficient Patients | Q54372222 | ||
| Increased acetylcholine sensitivity in Duchenne muscular dystrophy myotubes | Q57085856 | ||
| Properties of acetylcholine-receptor activation in human Duchenne muscular dystrophy myotubes | Q57085866 | ||
| Muscle glucose-6-phosphate dehydrogenase deficiency | Q57085868 | ||
| Recessive carnitine palmityl transferase deficiency: biochemical studies in tissue cultures and platelets | Q57085877 | ||
| Cytogenetic analysis and muscle differentiation in a girl with severe muscular dystrophy | Q57085885 | ||
| Analysis of fibronectin expression during human muscle differentiation | Q57085886 | ||
| Infantile-acute acid maltase deficiency (Pompe's disease): studies of muscle cultures | Q57085890 | ||
| Phosphofructokinase (PFK) deficiency due to a catalytically inactive mutant M-type subunit | Q57085898 | ||
| The homologue of the Duchenne locus is defective in X-linked muscular dystrophy of dogs | Q59051983 | ||
| Adult-onset acid maltase deficiency. Morphologic and biochemical abnormalities reproduced in in cultured muscle | Q66849146 | ||
| Characterization of dystrophin in muscle-biopsy specimens from patients with Duchenne's or Becker's muscular dystrophy | Q68137662 | ||
| Free cytoplasmic Ca++ at rest and after cholinergic stimulus is increased in cultured muscle cells from Duchenne muscular dystrophy patients | Q68278618 | ||
| Duchenne dystrophic muscle develops lesions in long-term coculture with mouse spinal cord | Q69670956 | ||
| Receptor-mediated uptake of acid alpha-glucosidase corrects lysosomal glycogen storage in cultured skeletal muscle | Q70060181 | ||
| Carnitine transport in cultured muscle cells and skin fibroblasts from patients with primary systemic carnitine deficiency | Q70452399 | ||
| Glycogen debrancher deficiency is reproduced in muscle culture | Q70545106 | ||
| Muscle carnitine deficiency: fatty acid metabolism in cultured fibroblasts and muscle cells | Q71233729 | ||
| Myoadenylate deaminase deficiency--muscle biopsy and muscle culture in a patient with gout | Q71304888 | ||
| Regional assignment of the human gene for platelet-type phosphofructokinase (PFKP) to chromosome 10p: novel use of polyspecific rodent antisera to localize human enzyme genes | Q72787832 | ||
| P433 | issue | 3 | |
| P304 | page(s) | 257-268 | |
| P577 | publication date | 1991-06-01 | |
| P1433 | published in | Italian journal of neurological sciences | Q27711320 |
| P1476 | title | Hereditary human myopathies in muscle culture | |
| P478 | volume | 12 |
| Q40102262 | Dissociated flexor digitorum brevis myofiber culture system--a more mature muscle culture system. | cites work | P2860 |
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