IL‐4/CCL22/CCR4 Axis Controls Regulatory T‐Cell Migration That Suppresses Inflammatory Bone Loss in Murine Experimental Periodontitis
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Published in Journal of bone and mineral research (01.03.2015)
Published in Journal of bone and mineral research (01.03.2015)
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Optimisation of the DNA dipstick as a rapid extraction method for Schistosoma japonicum in infected mice samples and spiked human clinical samples
Aula, Oyime P, McManus, Donald P, Jones, Malcolm K, You, Hong, Cai, Pengfei, Gordon, Catherine A
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Molecular identification of Ancylostoma ceylanicum in the Philippines
Aula, Oyime P., McManus, Donald P., Weerakoon, Kosala G., Olveda, Remigio, Ross, Allen G., Rogers, Madeleine J., Gordon, Catherine A.
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A new mtDNA mutation associated with Leber hereditary optic neuroretinopathy
HUOPONEN, K, VILKKI, J, AULA, P, NIKOSKELAINEN, E. K, SAVONTAUS, M.-L
Published in American journal of human genetics (01.06.1991)
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Published in American journal of human genetics (01.06.1991)
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Attitudes towards genetic testing: analysis of contradictions
Jallinoja, P., Hakonen, A., Aro, A.R., Niemelä, P., Hietala, M., Lönnqvist, J., Peltonen, L., Aula, P.
Published in Social science & medicine (1982) (01.05.1998)
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Phenotypic spectrum of Salla disease, a free sialic acid storage disorder
Varho, Tarja T., Alajoki, Liisa E., Posti, Kristiina M., Korhonen, Tapio T., Renlund, Martin G., Nyman, Samuel R.G., Sillanpää, Matti L., Aula, Pertti P.
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Central and peripheral nervous system dysfunction in the clinical variation of Salla disease
Varho, T, Jääskeläinen, S, Tolonen, U, Sonninen, P, Vainionpää, L, Aula, P, Sillanpää, M
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A mitochondrial mutation at nt 9101 in the ATP synthase 6 gene associated with deficient oxidative phosphorylation in a family with Leber hereditary optic neuroretinopathy
Lamminen, T, Majander, A, Juvonen, V, Wikström, M, Aula, P, Nikoskelainen, E, Savontous, M L
Published in American journal of human genetics (01.05.1995)
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Published in American journal of human genetics (01.05.1995)
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Acceptance of genetic testing in a general population: age, education and gender differences
Aro, A.R, Hakonen, A, Hietala, M, Lönnqvist, J, Niemelä, P, Peltonen, L, Aula, P
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Spectrum of Mutations in Aspartylglucosaminuria
IKONEN, E, AULA, P, GRON, K, TOLLERSRUD, O, HALILA, R, MANNINEN, T, SYVANEN, A.-C, PELTONEN, L
Published in Proceedings of the National Academy of Sciences - PNAS (15.12.1991)
Published in Proceedings of the National Academy of Sciences - PNAS (15.12.1991)
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A retrospective study of long-term psychosocial consequences and satisfaction after carrier testing in childhood in an autosomal recessive disease: aspartylglucosaminuria
Järvinen, O, Hietala, M, Aalto, A-M, Arvio, M, Uutela, A, Aula, P, Kääriäinen, H
Published in Clinical genetics (01.12.2000)
Published in Clinical genetics (01.12.2000)
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Convenient and quantitative determination of the frequency of a mutant allele using solid-phase minisequencing: Application to aspartylglucosaminuria in Finland
Syvänen, Ann-Christine, Ikonen, Elina, Manninen, Tuula, Bengtström, Marina, Söderlund, Hans, Aula, Pertti, Peltonen, Leena
Published in Genomics (San Diego, Calif.) (01.03.1992)
Published in Genomics (San Diego, Calif.) (01.03.1992)
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Deoxynivalenol alone or in combination with nivalenol and zearalenone induce systemic histological changes in pigs
Gerez, Juliana R., Pinton, Philippe, Callu, Patrick, Grosjean, François, Oswald, Isabelle P., Bracarense, Ana Paula F.L.
Published in Experimental and toxicologic pathology : official journal of the Gesellschaft für Toxikologische Pathologie (01.02.2015)
Published in Experimental and toxicologic pathology : official journal of the Gesellschaft für Toxikologische Pathologie (01.02.2015)
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Aspartylglucosaminuria: cDNA encoding human aspartylglucosaminidase and the missense mutation causing the disease
Ikonen, E, Baumann, M, Grön, K, Syvänen, A. C, Enomaa, N, Halila, R, Aula, P, Peltonen, L
Published in The EMBO journal (01.01.1991)
Published in The EMBO journal (01.01.1991)
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Reevaluation of the linkage of an optic atrophy susceptibility gene to X-chromosomal markers in Finnish families with Leber hereditary optic neuroretinopathy (LHON)
Juvonen, V, Vilkki, J, Aula, P, Nikoskelainen, E, Savontaus, M L
Published in American journal of human genetics (01.07.1993)
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Published in American journal of human genetics (01.07.1993)
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Phenotypic variation and magnetic resonance imaging (MRI) in Salla disease, a free sialic acid storage disorder
Haataja, L, Parkkola, R, Sonninen, P, Vanhanen, S L, Schleutker, J, Aärimaa, T, Turpeinen, U, Renlund, M, Aula, P
Published in Neuropediatrics (01.10.1994)
Published in Neuropediatrics (01.10.1994)
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Quality of life in caregivers of children and adolescents with Osteogenesis Imperfecta
Vanz, Ana Paula, Félix, Têmis M, da Rocha, Neusa Sica, Schwartz, Ida V D
Published in Health and quality of life outcomes (01.04.2015)
Published in Health and quality of life outcomes (01.04.2015)
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