Zobrazeno 1 - 10 of 124 pro vyhledávání: '"M L, Lokki"'
1
Akademický článek
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2
Mortality Rate Increases Steeply With Nonadherence to Statin Therapy in Patients With Acute Coronary Syndrome
Autor: Juha Sinisalo, Timo E. Strandberg, Olavi Parkkonen, Tero Hiekkalinna, Jaakko Allonen, Satu Vaara, Markku S. Nieminen, M. L. Lokki, Markus Perola
Publikováno v: Clinical Cardiology. 35:E22-E27
BACKGROUND: In a prospective cohort of consecutive acute coronary syndrome (ACS) patients, we compared the adherence rate of statin usage and mortality rate during a median follow‐up of 23 months. HYPOTHESIS: Adherence to statin therapy after acute
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c7a755657fdbc28ee32870eb058e764
https://doi.org/10.1002/clc.22056
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3
Akademický článek
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4
Evaluation of HLA-DRB1 imputation using a Finnish dataset
Autor: E, Vlachopoulou, E, Lahtela, A, Wennerström, A S, Havulinna, P, Salo, M, Perola, V, Salomaa, M S, Nieminen, J, Sinisalo, M-L, Lokki
Publikováno v: Tissue antigens. 83(5)
Owing to the vast amount of alleles, high-resolution human leukocyte antigen (HLA) typing is expensive and time-consuming. Scientists have attempted to develop computational approaches to define HLA alleles with high confidence. We tested the reliabi
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::11ef008879131450261bc10d203c0223
https://pubmed.ncbi.nlm.nih.gov/24666112
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5
16(th) IHIW: analysis of HLA population data, with updated results for 1996 to 2012 workshop data (AHPD project report)
Autor: Riitta Paakkanen, Grazia Nicoloso, Jose Manuel Nunes, Uma Kanga, Geoffrey K. Chambers, Antonij Slavcev, J.-F. Eliaou, I. Romón Alonso, Stéphane Buhler, N. Elamin, Narinder K. Mehra, Annika Wennerström, Maria Eugenia Riccio, Da Di, Manuela Testi, P. P. J. Dunn, Valérie Dubois, T. Suslova, M. Boldyreva, Jean-Marie Tiercy, L. Kolesar, Zorana Grubic, Lucie Richard, Christelle Vangenot, J. Di Cristofaro, Jacques Chiaroni, D. Papaioannou Voniatis, Mathias Currat, A. Varnavidou, C. Darke, C. Papasteriades, Taina Jaatinen, Alicia Sanchez-Mazas, M. S. Chernova, Marco Andreani, M. L. Lokki, W. Kunachiwa, Barbara Nelly Kervaire, B. Vidan-Jeras, G. Sulcebe, Hisham Atan Edinur, Mélanie Cuenod, F. Poli
Publikováno v: International Journal of Immunogenetics
International Journal of Immunogenetics, Wiley, 2013, 40 (1), pp.21-30. ⟨10.1111/iji.12033⟩
International Journal of Immunogenetics, Vol. 40 (2013) pp. 21-30
International Journal of Immunogenetics, 2013, 40 (1), pp.21-30. ⟨10.1111/iji.12033⟩
International journal of immunogenetics
International audience; We present here the results of the Analysis of HLA Population Data (AHPD) project of the 16th International HLA and Immunogenetics Workshop (16IHIW) held in Liverpool in May-June 2012. Thanks to the collaboration of 25 laborat
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a2a33866074518c96930a2f115cdb2f
https://hal.archives-ouvertes.fr/hal-00820070
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6
Strategies to work with HLA data in human populations for histocompatibility, clinical transplantation, epidemiology and population genetics: HLA-NET methodological recommendations
Autor: J.-F. Eliaou, E. Eglite, Denisa Mendonça, U Bekmane, A. Dormoy, G. Sulcebe, Søren Buus, B. Martins da Silva, Zorana Grubic, Francesca Poli, Jose Manuel Nunes, M. L. Lokki, Frans H.J. Claas, A.-M. van Walraven, Maria Eugenia Riccio, M. Ivanova, M. Toungouz Nevessignsky, C. Papasteriades, D. Papioannou Voniatis, Dário Ligeiro, Faviel F. Gonzalez-Galarza, AM Little, Valérie Dubois, Benedicte A. Lie, Alicia Sanchez-Mazas, Jean-Marie Tiercy, Gottfried Fischer, B. Vidan-Jeras, M. Spyropoulou Vlachou, Stéphane Buhler, Christelle Vangenot, Susan Tonks, Derek Middleton, J. Martorell
Publikováno v: International Journal of Immunogenetics, Vol. 39, No 6 (2012) pp. 459-476
International journal of immunogenetics
International journal of immunogenetics, 39 (6
International Journal of Immunogenetics
International Journal of Immunogenetics, 39(6), 459-476
HLA-NET (a European COST Action) aims at networking researchers working in bone marrow transplantation, epidemiology and population genetics to improve the molecular characterization of the HLA genetic diversity of human populations, with an expected
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::488e06254bcb48ca274913e129e6a837
https://archive-ouverte.unige.ch/unige:21982
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7
Lymphotoxin alpha LTA+496C allele is a risk factor for periodontitis in patients with coronary artery disease
Autor: Pirkko J. Pussinen, M. L. Lokki, Sirkka Asikainen, Juha Sinisalo, Susanna Paju, Mikko Seppänen, Anil Palikhe, Markku S. Nieminen, Jari Ahlberg, Ville Valtonen
Publikováno v: Tissue antigens. 71(6)
Periodontitis and coronary artery disease (CAD) are inflammatory diseases and associated with each other. The major histocompatibility complex (MHC) region carries genes involved in immune response and inflammation. We investigated whether the MHC ge
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d75fa8353a66ef069fbe464356befd71
https://pubmed.ncbi.nlm.nih.gov/18384488
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9
Deficiency of human complement protein C4 due to identical frameshift mutations in the C4A and C4B genes
Autor: M L, Lokki, A, Circolo, P, Ahokas, K L, Rupert, C Y, Yu, H R, Colten
Publikováno v: Journal of immunology (Baltimore, Md. : 1950). 162(6)
The complement protein C4, encoded by two genes (C4A and C4B) on chromosome 6p, is the most polymorphic among the MHC III gene products. We investigated the molecular basis of C4 deficiency in a Finnish woman with systemic lupus erythematosus. C4-spe
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::fb713fb6cbdf0999ea29ba0147ced1ee
https://pubmed.ncbi.nlm.nih.gov/10092831
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10
Molecular heterogeneity in deficiency of complement protein C2 type I
Autor: X, Wang, A, Circolo, M L, Lokki, P G, Shackelford, R A, Wetsel, H R, Colten
Publikováno v: Immunology. 93(2)
Deficiency of the complement protein C2 (C2D), one of the most common genetic deficiencies of the complement system, is associated with rheumatological disorders and increased susceptibility to infection. Two types of C2D have been recognized, each i
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::ddaa87d295ae75cab641592f19a358b7
https://pubmed.ncbi.nlm.nih.gov/9616367
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