Search Results - "Halila, R"

Ethically problematic treatment decisions in different medical specialties by Saarni, S I, Halila, R, Palmu, P, Vänskä, J

“…Background: Ethical dilemmas are an integral part of medicine. Whether physicians actually feel that they have made ethically problematic treatment decisions…”
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Serum procollagen type III is an early and sensitive marker for veno-occlusive disease of the liver in children undergoing bone marrow transplantation by HEIKINHEIMO, M, HALILA, R, FASTH, A

“…Veno-occlusive disease of the liver (VOD) is a life-threatening complication occurring in patients undergoing bone marrow transplantation (BMT). Although…”
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Spectrum of Mutations in Aspartylglucosaminuria by IKONEN, E, AULA, P, GRON, K, TOLLERSRUD, O, HALILA, R, MANNINEN, T, SYVANEN, A.-C, PELTONEN, L

“…Aspartylglucosaminuria (AGU) is an inherited lysosomal storage disorder caused by the deficiency of aspartylglucosaminidase. We have earlier reported a single…”
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Aspartylglucosaminuria: cDNA encoding human aspartylglucosaminidase and the missense mutation causing the disease by Ikonen, E, Baumann, M, Grön, K, Syvänen, A. C, Enomaa, N, Halila, R, Aula, P, Peltonen, L

“…We have isolated a 2.1 kb cDNA which encodes human aspartylglucosaminidase (AGA, E.C. 3.5.1.26). The activity of this lysosomal enzyme is deficient in…”
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Human leucocyte aspartylglucosaminidase. Evidence for two different subunits in a more complex native structure by Halila, R, Baumann, M, Ikonen, E, Enomaa, N, Peltonen, L

“…Human leucocyte aspartylglucosaminidase (AGA: 1-aspartamido-beta-N-acetylglucosamine amidohydrolase, EC 3.5.1.26) was purified to homogeneity by using affinity…”
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Purification of human procollagen type III N-proteinase from placenta and preparation of antiserum by Halila, R, Peltonen, L

“…Procollagen type III N-proteinase, of Mr about 70,000, was detected in human placental tissue and purified from this source more than 5800-fold. It was found…”
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Enzymes converting procollagens to collagens by Peltonen, L, Halila, R, Ryhänen, L

“…Conversion from procollagen to collagen is a specific process that is a requirement for proper alignment of collagen molecules to form functional fibers. This…”
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Neutral protease cleaving the N-terminal propeptide of type III procollagen: partial purification and characterization of the enzyme from smooth muscle cells of bovine aorta by Halila, R, Peltonen, L

“…Procollagen type III amino-terminal protease was detected in cultures of smooth muscle cells of fetal calf aorta, and this protease was purified about…”
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Human aspartylglucosaminidase : a biochemical and immunocytochemical characterization of the enzyme in normal and aspartylglucosaminuria fibroblasts by ENOMAA, N, HEISKANEN, T, HALILA, R, SORMUNEN, R, SEPPÄLÄ, R, VIHINEN, M, PELTONEN, L

“…Aspartylglucosaminidase (AGA, EC 3.5.1.26) is an essential enzyme in the degradation of asparagine-linked glycoproteins. In man, deficient activity of this…”
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Processing of types I and III procollagen in Ehlers-Danlos syndrome type VII by HALILA, R, STEINMANN, B, PELTONEN, L

“…The processing of types I and III procollagen was studied in skin fibroblast cultures from type VII A and B of the Ehlers-Danlos syndrome [EDS] and age-matched…”
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The Role of National Ethics Commissions in Finland by Halila, Ritva

“…There are six national ethics commissions in Finland. The National Advisory Board on Research Ethics was first established in 1991, followed by the National…”
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Expanding screening for rare metabolic disease in the newborn : An analysis of costs, effect and ethical consequences for decision-making in Finland by AUTTI-RÄMÖ, Ilona, MÄKELÄ, Marjukka, RENLUND, Martin, SALO, Matti, TYNI, Tiina, SINTONEN, Harri, KOSKINEN, Hanna, LAAJALAHTI, Liisa, HALILA, Ritva, KÄÄRIÄINEN, Helena, LAPATTO, Risto, NÄNTÖ-SALONEN, Kirsti, PULKXI, Kari

“…Currently, the only metabolic disorder that newborns are screened for in Finland is congenital hypothyroidism. A proposal to start a pilot study on screening…”
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Why Shouldn't Children Decide Whether They Are Enrolled in Nonbeneficial Medical Research? by Halila, Ritva, Lötjönen, Salla

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Aspartylglucosaminuria (AGU): protein and gene structure of normal and mutated aspartylglucosaminidase by Halila, R, Ikonen, E, Tollersrud, O, Syvänen, A C, Enomaa, N, Peltonen, L

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A sensitive and rapid method for assaying the activity of type III procollagen amino-terminal proteinase by Halila, R

“…A rapid assay procedure was developed for measuring the rate of cleavage of the amino-terminal propeptide of type III procollagen. The method was based on the…”
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Molecular cloning, expression and chromosomal localization of a human gene encoding a 33 kDa putative metallopeptidase (PRSM1) by Scott, Ian C., Halila, Ritva, Jenkins, Joanne M., Mehan, Sharon, Apostolou, Sinoula, Winqvist, Robert, Callen, David F., Prockop, Darwin J., Peltonen, Leena, Kadler, Karl E.

“…The zincins are a superfamily of structurally-related Zn 2+-binding metallopeptidases which play a major role in a wide range of biological processes including…”
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N-terminal propeptide of type III collagen in tracheal fluid and serum in preterm infants at risk for bronchopulmonary dysplasia by HEIKINHEIMO, M, HALILA, R, MARTTINEN, E, RAIVIO, K

“…Bronchopulmonary dysplasia (BPD) is a common pulmonary complication in preterm infants that leads to fibrosis of the bronchoalveolar walls and often to severe…”
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Human leucocyte aspartylglycosaminidase : evidence for two different subunits in a more complex native structure by HALILA, R, BAUMANN, M, IKONEN, E, ENOMAA, N, PELTONEN, L

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Aspartylglucosaminuria : cDNA encoding human aspartylgucosaminidase and the missense mutation causing the disease by IKONEN, E, BAUMANN, M, GROÊN, K, SYVAÊNEN, A.-C, ENOMAA, N, HALILA, R, AULA, P, PELTONEN, L

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The human gene for xanthine dehydrogenase (XDH) is localized on chromosome band 2q22 by Rytkönen, E M, Halila, R, Laan, M, Saksela, M, Kallioniemi, O P, Palotie, A, Raivio, K O

“…Mutations in the xanthine dehydrogenase gene (XDH), which codes for the last enzyme of the purine catabolic pathway in man, cause the autosomal recessive…”
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