Published in Biochem J on June 15, 1982
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An affinity-column procedure using poly(L-proline) for the purification of prolyl hydroxylase. Purification of the enzyme from chick embryos. Eur J Biochem (1975) 1.80
The kinetics of disappearance of labeled leucine from the free leucine pool of rat liver and its effect on the apparent turnover of catalase and other hepatic proteins. J Biol Chem (1971) 1.70
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Radiommunoassay for human and chick prolyl hydroxylases. Eur J Biochem (1975) 1.17
Partial purification and characterization of peptidyl proline hydroxylase precursor from mouse fibroblasts. Arch Biochem Biophys (1972) 1.03
The assembly of tetrameric prolyl hydroxylase in tendon fibroblasts from newly synthesized alpha-subunits and from preformed cross-reacting protein. Biochem J (1980) 1.01
Regulation of collagen post-translational modification in transformed human and chick-embryo cells. Biochem J (1981) 0.98
Developmental changes in prolyl hydroxylase activity and protein in chick embryo. Eur J Biochem (1976) 0.96
Immunoreactive prolyl hydroxylase in human skin, serum and synovial fluid: changes in the content and components with age. Eur J Clin Invest (1977) 0.94
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Tetramers and monomers of prolyl hydroxylase in isolated chick-embryo tendon cells. The association of inactive monomers to active tetramers and a preliminary characterization of the intracellular monomer-size protein. Eur J Biochem (1977) 0.89
Turnover of prolyl hydroxylase and an immunologically related protein in rabbit tissue. Biochim Biophys Acta (1979) 0.82
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A 3-year clinical follow-up of adult patients with 3243A>G in mitochondrial DNA. Neurology (2006) 1.58
The 2-oxoglutarate binding site of prolyl 4-hydroxylase. Identification of distinct subsites and evidence for 2-oxoglutarate decarboxylation in a ligand reaction at the enzyme-bound ferrous ion. Eur J Biochem (1984) 1.56
Ascorbate is consumed stoichiometrically in the uncoupled reactions catalyzed by prolyl 4-hydroxylase and lysyl hydroxylase. J Biol Chem (1984) 1.50
Separate binding sites for nuclear factor 1 and a CCAAT DNA binding factor in the mouse alpha 2(I) collagen promoter. J Biol Chem (1987) 1.47
A novel mitochondrial DNA mutation and a mutation in the Notch3 gene in a patient with myopathy and CADASIL. J Mol Med (Berl) (2001) 1.46
Phylogenetic network of the mtDNA haplogroup U in Northern Finland based on sequence analysis of the complete coding region by conformation-sensitive gel electrophoresis. Am J Hum Genet (2000) 1.45
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Reduction of collagen production in keloid fibroblast cultures by ethyl-3,4-dihydroxybenzoate. Inhibition of prolyl hydroxylase activity as a mechanism of action. J Biol Chem (1987) 1.25
Apparent diffusion coefficients and T2 relaxation time measurements to evaluate disc degeneration. A quantitative MR study of young patients with previous vertebral fracture. Acta Radiol (2001) 1.23
Synthesis and degradation of type I procollagen mRNAs in cultured human skin fibroblasts and the effect of cortisol. J Biol Chem (1985) 1.22
Phylogenetic analysis of mitochondrial DNA in patients with an occipital stroke. Evaluation of mutations by using sequence data on the entire coding region. Mutat Res (2001) 1.18
APP locus duplication in a Finnish family with dementia and intracerebral haemorrhage. J Neurol Neurosurg Psychiatry (2007) 1.17
Evidence for mtDNA admixture between the Finns and the Saami. Hum Hered (2001) 1.16
Differences between collagen hydroxylases and 2-oxoglutarate dehydrogenase in their inhibition by structural analogues of 2-oxoglutarate. Biochem J (1985) 1.13
Partial purification and characterization of chick-embryo prolyl 3-hydroxylase. Biochem J (1979) 1.08
Histone H1 binds to the putative nuclear factor I recognition sequence in the mouse alpha 2(I) collagen promoter. J Biol Chem (1989) 1.01
Hereditary dementia with intracerebral hemorrhages and cerebral amyloid angiopathy. Neurology (2004) 1.01
Mitochondrial DNA haplogroup U as a risk factor for occipital stroke in migraine. Lancet (1998) 1.01
Detection of meningeal fibrosis after subarachnoid haemorrhage by assaying procollagen propeptides in cerebrospinal fluid. J Neurol Neurosurg Psychiatry (1999) 1.01
Phylogenetic analysis of mtDNA haplogroup TJ in a Finnish population. J Hum Genet (2001) 1.01
Cortisol decreases the concentration of translatable type-I procollagen mRNA species in the developing chick-embryo calvaria. Biochem J (1981) 0.99
Ultrasound-controlled neuronavigator-guided brain surgery. J Neurosurg (1993) 0.99
Glucocorticoid action on connective tissue: from molecular mechanisms to clinical practice. Med Biol (1986) 0.96
Prevalence of large-scale mitochondrial DNA deletions in an adult Finnish population. Neurology (2005) 0.95
Transient increase in procollagen propeptides in the CSF after subarachnoid hemorrhage. Neurology (2000) 0.92
Causes of death in pedigrees with the 3243A>G mutation in mitochondrial DNA. J Neurol Neurosurg Psychiatry (2008) 0.92
Familial aggregation of Parkinson's disease in a Finnish population. J Neurol Neurosurg Psychiatry (2000) 0.92
Hearing impairment in patients with 3243A-->G mtDNA mutation: phenotype and rate of progression. Hum Genet (2001) 0.91
Promoter of the gene for the multifunctional protein disulfide isomerase polypeptide. Functional significance of the six CCAAT boxes and other promoter elements. J Biol Chem (1992) 0.91
Prolyl 3-hydroxylase and 4-hydroxylase activities in certain rat and chick-embryo tissues and age-related changes in their activities in the rat. Biochem J (1979) 0.91
Turnover of prolyl hydroxylase tetramers and the monomer-size protein in chick-embryo cartilaginous bone and lung in vivo. Biochem J (1979) 0.91
Complex segregation analysis of Parkinson's disease in the Finnish population. Hum Genet (2001) 0.90
Analysis of mitochondrial DNA sequences in patients with isolated or combined oxidative phosphorylation system deficiency. J Med Genet (2006) 0.89
Rapid induction of meningeal collagen synthesis in the cerebral cisternal and ventricular compartments after subarachnoid hemorrhage. Acta Neurochir (Wien) (2001) 0.88
Increase of collagen synthesis and deposition in the arachnoid and the dura following subarachnoid hemorrhage in the rat. Biochim Biophys Acta (1999) 0.88
A rapid and sensitive assay for protein disulphide isomerase activity. J Biochem Biophys Methods (1983) 0.87
Frequency of mitochondrial DNA point mutations among patients with familial sensorineural hearing impairment. Eur J Hum Genet (2000) 0.87
High concentrations of procollagen propeptides in chronic subdural haematoma and effusion. J Neurol Neurosurg Psychiatry (2003) 0.86
The 90 kDa heat shock protein (hsp90) induces the condensation of the chromatin structure. Biochem Biophys Res Commun (1994) 0.86
Mutations in EIF4G1 are not a common cause of Parkinson's disease. Eur J Neurol (2013) 0.85
Childhood encephalopathies and myopathies: a prospective study in a defined population to assess the frequency of mitochondrial disorders. Pediatrics (2000) 0.85
Increased activities of antioxidant enzymes and decreased ATP concentration in cultured myoblasts with the 3243A-->G mutation in mitochondrial DNA. Biochim Biophys Acta (2000) 0.85
Modulation of glucocorticoid receptor activity by cyclic nucleotides and its implications on the regulation of human skin fibroblast growth and protein synthesis. Biochim Biophys Acta (1984) 0.85
Interactions of Hsp90 with histones and related peptides. Life Sci (1999) 0.85
Computed tomography data based rapid prototyping model of the temporal bone before cochlear implant surgery. Acta Otolaryngol Suppl (1997) 0.85
Mutations in CHMP2B are not a cause of frontotemporal lobar degeneration in Finnish patients. Eur J Neurol (2010) 0.84
Regulation of type IV collagen degrading enzyme by cortisol during human skin fibroblast growth. Biochem Biophys Res Commun (1985) 0.84
No association of the mitochondrial DNA A12308G polymorphism with increased risk of stroke in patients with the A3243G mutation. J Neurol Neurosurg Psychiatry (2004) 0.84
Effects of laminin, proteoglycan and type IV collagen, components of basement membranes, on platelet aggregation. Biochem Biophys Res Commun (1981) 0.84
Relative fitness of carriers of the mitochondrial DNA mutation 3243A > G. Eur J Hum Genet (2001) 0.84
Experimental spinal fusion with decalcified bone matrix and deep-frozen allogeneic bone in rabbits. Clin Orthop Relat Res (1982) 0.83
Low prevalence of progranulin mutations in Finnish patients with frontotemporal lobar degeneration. Eur J Neurol (2008) 0.83
Connective tissue metabolites in serum as markers of disease activity in patients with rheumatoid arthritis. Clin Exp Rheumatol (1988) 0.82
Nucleoside triphosphate binding and hydrolysis by histone H1. Biochem Biophys Res Commun (1992) 0.82
The bone inductive capacity of various bone transplanting materials used for treatment of experimental bone defects. Clin Orthop Relat Res (1979) 0.82
Nucleotide and calcium-induced conformational changes in histone H1. FEBS Lett (1997) 0.81
Synthesis of collagen: chemical regulation of post-translational events. Ciba Found Symp (1985) 0.80
Parkinsonism associated with the homozygous W748S mutation in the POLG1 gene. Parkinsonism Relat Disord (2008) 0.80
Cortisol induces (2'-5')oligoadenylate synthetase in cultured chick embryo tendon fibroblasts. Biochem Biophys Res Commun (1982) 0.80
Restriction fragment analysis as a source of error in detection of heteroplasmic mtDNA mutations. Mutat Res (1999) 0.80
Interaction of transcription factor Sp1 with the promoter of the gene for the multifunctional protein disulphide isomerase polypeptide. Biochem J (1993) 0.79
Mitochondrial DNA deletion diagnosed by analysis of an endomyocardial biopsy specimen from a patient with Kearns-Sayre syndrome and complete heart block. Br Heart J (1992) 0.79
Steroid-involved transcriptional regulation of human genes encoding prostatic acid phosphatase, prostate-specific antigen, and prostate-specific glandular kallikrein. Endocrinology (1997) 0.79
Modifier locus for mitochondrial DNA disease: linkage and linkage disequilibrium mapping of a nuclear modifier gene for maternally inherited deafness. Genet Med (2001) 0.78
Ubiquinone and nicotinamide treatment of patients with the 3243A-->G mtDNA mutation. Neurology (2002) 0.78
Coordination of transcription of the human 17 beta-hydroxysteroid dehydrogenase type 1 gene (EDH17B2) by a cell-specific enhancer and a silencer: identification of a retinoic acid response element. Mol Endocrinol (1995) 0.77
Haplotype-matched controls as a tool to discriminate polymorphisms from pathogenic mutations in mtDNA. Hum Genet (1999) 0.77
Increased risk of sensorineural hearing loss and migraine in patients with a rare mitochondrial DNA variant 4336A>G in tRNAGln. J Med Genet (2001) 0.77
The ATP/ADP binding domains of actin are conserved in nucleosome complexed with histone H1 and high mobility group-17 protein. Biochem Biophys Res Commun (1995) 0.76
Voxelwise analysis of diffusion tensor imaging and structural MR imaging in patients with the m.3243A>G mutation in mitochondrial DNA. AJNR Am J Neuroradiol (2011) 0.76
Specific non-enzymatic glycation of the rat histone H1 nucleotide binding site in vitro in the presence of AlF4-. A putative mechanism for impaired chromatin function. Biochim Biophys Acta (1993) 0.76
Familial aggregation of cervical artery dissection and cerebral aneurysm. Stroke (1994) 0.76
Molecular genetic analysis of the alpha-synuclein and the parkin gene in Parkinson's disease in Finland. Eur J Neurol (2002) 0.76
DNA binding of histone H1 is modulated by nucleotides. FEBS Lett (1992) 0.76
Adult-onset diabetes mellitus and neurosensory hearing loss in maternal relatives of MELAS patients in a family with the tRNA(Leu(UUR)) mutation. Neurology (1993) 0.75
Regulation of proline 3-hydroxylation and prolyl 3-hydroxylase and 4-hydroxylase activities in transformed cells. Biochem J (1982) 0.75
Variations of mitochondrial DNA polymerase γ in patients with Parkinson's disease. J Neurol (2013) 0.75
Effect of prevention of procollagen triple-helix formation on proline 3-hydroxylation in freshly isolated chick-embryo tendon cells. Biochem J (1981) 0.75
[Virtual reality in radiology]. Duodecim (1997) 0.75
Repair of bone defects by bone inductive material. Acta Orthop Scand (1979) 0.75
Nucleotide recognition by histone H1 involves specific protein structures. Arch Biochem Biophys (1995) 0.75
Neuronavigator-guided cerebral biopsy. Acta Neurochir Suppl (Wien) (1993) 0.75
Retracted Nucleotide recognition by histone H1 involves specific protein structures. Arch Biochem Biophys (1994) 0.75
Homology of histone H1 variants with adenine nucleotide-binding proteins. Biochem Biophys Res Commun (1988) 0.75
Epidemiology of the mitochondrial DNA 8344A>G mutation for the myoclonus epilepsy and ragged red fibres (MERRF) syndrome. J Neurol Neurosurg Psychiatry (2003) 0.75
Kearns-Sayre syndrome case presenting a mitochondrial DNA deletion with unusual direct repeats and a rudimentary RNAase mitochondrial ribonucleotide processing target sequence. Genomics (1993) 0.75
The Finnish speech-in-noise test in MELAS mutation and other sensorineural hearing impairments. Scand Audiol Suppl (2001) 0.75
The histone H1-lacZ' fusion protein produced in Escherichia coli binds to the 5'-TTGGCAnnnTGCCAA-3' motif on DNA. FEBS Lett (1991) 0.75
Cortisol decreases the cellular concentration of translatable procollagen mRNA species in cultured human skin fibroblasts. Biochim Biophys Acta (1983) 0.75
[Structure and biosynthesis of collagen]. Duodecim (1980) 0.75
Interference of AlF4- with nucleotide and DNA binding of rat histone H1 in vitro. Implications for the pathogenesis of Alzheimer's disease. Neurosci Lett (1991) 0.75
The bone inductive capacity of decalcified bone matrix modified by diphenylhydantoin. Acta Orthop Scand (1981) 0.75