Published in Arch Biochem Biophys on November 01, 1973
Basal bioenergetic abnormalities in skeletal muscle from ryanodine receptor malignant hyperthermia-susceptible R163C knock-in mice. J Biol Chem (2010) 0.91
Parathyroid ablation in dystrophic hamsters. Effects on Ca content and histology of heart, diaphragm, and rectus femoris. J Clin Invest (1981) 0.89
The respiration and calcium content of heart mitochondria from rats with vitamin D-induced cardionecrosis. Biochem J (1985) 0.85
The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion. Am J Hum Genet (1989) 5.09
Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy. Nature (1986) 4.13
Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPs. Lancet (1985) 3.08
Mitochondrial calcium overload: A general mechanism for cell-necrosis in muscle diseases. Lancet (1976) 2.22
Reversible inhibition of mitochondrial adenosine diphosphate phosphorylation by long chain acyl coenzyme A esters. J Biol Chem (1971) 1.64
Prostaglandin and thromboxane synthesis in a pure macrophage population and the inhibition, by E-type prostaglandins, of chemiluminescence. FEBS Lett (1978) 1.55
Comparison of the segregation of the RYR1 C1840T mutation with segregation of the caffeine/halothane contracture test results for malignant hyperthermia susceptibility in a large Manitoba Mennonite family. Anesthesiology (1996) 1.48
Regional localization of 18 human X-linked DNA sequences. Cytogenet Cell Genet (1986) 1.48
Serum CK, calcium, magnesium, and oxidative phosphorylation in mdx mouse muscular dystrophy. Muscle Nerve (1988) 1.36
Identical mutation in patients with limb girdle muscular dystrophy type 2B or Miyoshi myopathy suggests a role for modifier gene(s). Hum Mol Genet (1999) 1.31
Identical dysferlin mutation in limb-girdle muscular dystrophy type 2B and distal myopathy. Neurology (2000) 1.25
Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies). Neuromuscul Disord (2000) 1.22
Limb-girdle muscular dystrophy and Miyoshi myopathy in an aboriginal Canadian kindred map to LGMD2B and segregate with the same haplotype. Am J Hum Genet (1996) 1.20
Haematological Values. Can Med Assoc J (1953) 1.15
Recombinations in individuals homozygous by descent localize the Friedreich ataxia locus in a cloned 450-kb interval. Am J Hum Genet (1994) 1.14
Segregation analysis of a marker localised Xp21.2-Xp21.3 in Duchenne and Becker muscular dystrophy families. Hum Genet (1985) 1.09
DNA studies in a family with Duchenne muscular dystrophy and a deletion at Xp21. Am J Hum Genet (1987) 1.08
Three years' experience with neonatal screening for Duchenne/Becker muscular dystrophy: gene analysis, gene expression, and phenotype prediction. Am J Med Genet (1991) 1.03
Chemiluminescence and immune cell activation. I. Early activation of rat thymocytes can be monitored by chemiluminescence measurements. Eur J Immunol (1978) 1.02
Preferential loss of ATP-dependent long-chain fatty acid activating enzyme in mitochondria prepared using Nagarse. Biochim Biophys Acta (1970) 1.01
Multipoint genetic mapping of the Xq26-q28 region in families with fragile X mental retardation and in normal families reveals tight linkage of markers in q26-q27. Hum Genet (1987) 1.00
Gene studies in newborn males with Duchenne muscular dystrophy detected by neonatal screening. Lancet (1988) 0.97
A gene for autosomal recessive limb-girdle muscular dystrophy in Manitoba Hutterites maps to chromosome region 9q31-q33: evidence for another limb-girdle muscular dystrophy locus. Am J Hum Genet (1998) 0.94
Chemiluminescence and immune cell activation. II. Enhancement of concanavalin A-induced chemiluminescence following in vitro preincubation of rat thymocytes; dependency on macrophage-lymphocyte interaction. Eur J Immunol (1980) 0.92
Metabolic reduction of 4-nitroquinoline N-oxide and other radical-producing drugs to oxygen-reactive intermediates. Cancer Res (1977) 0.92
A calcium-associated magnesium-responsive defect of respiration and oxidative phosphorylation by skeletal muscle mitochondria of BIO 14.6 dystrophic hamsters. Life Sci II (1970) 0.89
The 56/58 kDa androgen-binding protein in male genital skin fibroblasts with a deleted androgen receptor gene. Mol Cell Endocrinol (1991) 0.88
The Friedreich ataxia region: characterization of two novel genes and reduction of the critical region to 300 kb. Hum Mol Genet (1994) 0.88
Impact of genetic counselling after neonatal screening for Duchenne muscular dystrophy. J Med Genet (1993) 0.87
Kinetics of NADH oxidation by pigeon-heart mitochondria. Can J Biochem (1967) 0.87
Mitochondrial calcium overloading in cardiomyopathic hamsters. J Mol Cell Cardiol (1978) 0.86
Carbohydrate and fat in energy metabolism of red and white muscle. Am J Physiol (1971) 0.86
Respiration and oxidative phosphorylation by mitochondria of red and white skeletal muscle. Can J Biochem (1970) 0.86
Transcarboxylase. 8. Isolation and properties of a biotin-carboxyl carrier protein. Proc Natl Acad Sci U S A (1969) 0.85
Concanavalin A-induced chemiluminescence in rat thymus lymphocytes. Its origin and role in mitogenesis. Biochem J (1981) 0.85
Amber mutation creates a diagnostic MaeI site in the androgen receptor gene of a family with complete androgen insensitivity. Am J Med Genet (1991) 0.85
Limb girdle muscular dystrophy in Manitoba Hutterites does not map to any of the known LGMD loci. Am J Med Genet (1997) 0.84
Dysferlin expression after normal myoblast transplantation in SCID and in SJL mice. Neuromuscul Disord (2002) 0.84
Transcarboxylase. XII. Identification of the metal-containing subunits of transcarboxylase and stability of the binding. J Biol Chem (1972) 0.83
Factors influencing the utilization of reduced nicotinamide adenine dinucleotide by pigeon heart mitochondria. Can J Biochem (1966) 0.83
The 56 kDa androgen binding protein is an aldehyde dehydrogenase. Biochem Biophys Res Commun (1991) 0.82
Oxidative phosphorylation by muscle mitochondria of dysstrophic mice. Can J Biochem (1967) 0.82
Oxidative phosphorylation in smooth muscle. Am J Physiol (1970) 0.82
Biochemical investigations in cultured skin fibroblasts from patients with Duchenne muscular dystrophy. Clin Genet (1978) 0.81
Leu-676-Pro mutation of the androgen receptor causes complete androgen insensitivity syndrome in a large Hutterite kindred. Hum Mutat (1995) 0.81
Oxidative phosphorylation in cardiomyopathic hamsters. Am J Physiol (1972) 0.81
Glycogen and CO-2 production from glucose and lactate by red and white skeletal muscle. Am J Physiol (1965) 0.80
Misleading second-stage Schilling tests due to inactive intrinsic factor concentrate. Ann Intern Med (1979) 0.80
Analysis of the CAG repeat region of the androgen receptor gene in a kindred with X-linked spinal and bulbar muscular atrophy. J Neurol Sci (1992) 0.79
An XmnI RFLP at the subtelomeric Xp locus DXS31 [HGM7, LA, 1985]. Nucleic Acids Res (1986) 0.79
Differing populations of mitochondria isolated from the skeletal muscle of normal and dystrophic hamsters. Can J Biochem (1974) 0.79
Falsely negative laboratory diagnosis for myocardial infarction owing to the concurrent presence of macro creatine kinase and macro lactate dehydrogenase. Clin Chem (1982) 0.78
Altered amounts of hemoglobin synthesis in livers of dystrophic hamsters. Can J Biochem (1977) 0.78
Perinatal changes in a digoxin-like immunoreactive substance. Pediatr Res (1984) 0.78
56K fibroblast protein not specific for Duchenne muscular dystrophy but for skin biopsy site. Nature (1983) 0.78
Respiration and oxidative phosphorylation by muscle and heart mitochondria of hamsters with hereditary myocardiopathy and polymyopathy. Can J Biochem (1968) 0.77
Analysis of fibroblast proteins from patients with Duchenne muscular dystrophy by two-dimensional gel electrophoresis. Nature (1982) 0.77
Proline incorporation by cultured skin fibroblasts from patients with duchenne muscular dystrophy. J Neurol Sci (1983) 0.77
The stimulation by phosphate and the inhibition by adenine nucleotides and nicotinamide-adenine dinucleotide of the respiratory chain. Can J Biochem (1968) 0.77
Defective respiration and oxidative phosphorylation in muscle mitochondria of hamsters in the late stages of hereditary muscular dystrophy. Can J Biochem (1970) 0.77
Single-blind study of dystrophin staining in carriers of Duchenne muscular dystrophy. Can J Neurol Sci (1993) 0.75
Human cytosolic aldehyde dehydrogenase in androgen insensitivity syndrome. Adv Exp Med Biol (1993) 0.75
On the role of mitochondria in the hereditary cardiomyopathy of the Syrian hamster. Recent Adv Stud Cardiac Struct Metab (1975) 0.75
The 56 kDa androgen-binding protein in human genital skin fibroblasts: its relation to the human androgen receptor. Mol Cell Endocrinol (1990) 0.75
A TaqI RFLP in Xq26-Xqter detected by pX45h [HGM8 no. DXS100h]. Nucleic Acids Res (1986) 0.75
Oxidative phosphorylation by mitochondria isolated from hearts of BIO 14.6 myopathic hamsters. Trans N Y Acad Sci (1968) 0.75
Searching for molecular abnormalities in genetic diseases by the use of a double labeling technique. II. Deficiency of a basic protein in fibroblasts of patients with Pompe's disease. Pediatr Res (1978) 0.75
Effect of assay conditions on cross reactivity of digoxin-like immunoreactive substance(s) with radioimmunoassay kits. Clin Chem (1985) 0.75
Mitochondrial calcium content and oxidative phosphorylation in heart and skeletal muscle of dystrophic mice. Exp Neurol (1983) 0.75
A study of androgen-resistant subjects indicates that the 6.7 pI/56 kDa protein in genital skin fibroblasts is related to the androgen receptor. Clin Invest Med (1988) 0.75
Ouabain inhibition of adenosine triphosphatase in erythrocyte membranes from dystrophic hamsters. Enzyme (1972) 0.75
Functional studies on in situ-like mitochondria isolated in the presence of polyvinyl pyrrolidone. Biochim Biophys Acta (1985) 0.75
Searching for molecular abnormalities in genetic diseases by the use of a double labeling technique. I. Rationale, techniques, and initial evaluation. Pediatr Res (1978) 0.75
Is there a calcium-caused defect of oxidative phosphorylation in cardiomyopathic hamster hearts? Recent Adv Stud Cardiac Struct Metab (1978) 0.75
Abnormal oxidative phosphorylation in skeletal muscle mitochondria of the BIO 14.6 dystrophic Syrian hamster. Recent Adv Stud Cardiac Struct Metab (1972) 0.75
A role for clinical case simulations in basic medical science education. Physiologist (1985) 0.75
Oxidative phosphorylation at various stages of genetically determined cardiomyopathy in the Syrian hamster. Recent Adv Stud Cardiac Struct Metab (1973) 0.75
Biochemical aspects of muscle necrosis in hamster dystrophy. Ann N Y Acad Sci (1979) 0.75
Sarcolemmal ATPase activities in normal and BIO 14.6 dystrophic hamster skeletal muscle. Can J Biochem (1974) 0.75
A magnesium-responsive defect of respiration and oxidative phosphorylation in skeletal muscle mitochondria of dystrophic hamsters. Can J Biochem (1970) 0.75
SCINT II; an improved program for the statistical analysis and plotting of variably quenched dual-labeled liquid scintillation samples. Anal Biochem (1977) 0.75
Effect of ruthenium red on oxidative phosphorylation and the calcium and magnesium content of skeletal muscle mitochondria of normal and BIO 14.6 dystrophic hamsters. Biochim Biophys Acta (1973) 0.75
Partial androgen insensitivity--are all tissues equal? Fertil Steril (1993) 0.75
A study into the nature and organ source of digoxin-like immunoreactive substance(s) in the perinatal period. Biol Neonate (1989) 0.75