Search Results - "HOLOPAINEN, P."

Space-Vector Models for Torsional Vibration of Cage Induction Motors by Arkkio, Antero, Holopainen, Timo P.

“…Electromagnetic response of induction motors to torsional vibration is studied using space-vector and finite-element (FE) models. Comparison of the results…”
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Additional Losses of Electrical Machines Under Torsional Vibration by Arkkio, Antero, Cederstrom, Samuli, Awan, Hafiz Asad Ali, Saarakkala, Seppo E., Holopainen, Timo P.

“…Electric drive trains have a torsional rigid-body vibration mode at a small, nonzero frequency. If an excitation occurs close to this frequency, the vibration…”
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Genetic association of coeliac disease susceptibility to polymorphisms in the ICOS gene on chromosome 2q33 by Haimila, K, Smedberg, T, Mustalahti, K, Mäki, M, Partanen, J, Holopainen, P

“…An interesting candidate gene region for coeliac disease (CD), a common multifactorial disease, is a segment on 2q33-37 harbouring the genes for the CD28,…”
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Technical Note: Linkage Disequilibrium and Disease-Associated CTLA4 Gene Polymorphisms by Holopainen, Paivi M, Partanen, Jukka A

“…CTLA4 and CD28 are important regulators of T lymphocyte activation. Gene region 2q33 carrying genes for both CTLA4 and CD28 has been shown to be linked to many…”
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Electromechanical interaction in rotordynamics of cage induction motors by Holopainen, Timo P., Tenhunen, Asmo, Arkkio, Antero

“…Eccentric rotor motion induces an unbalanced magnetic pull between the rotor and stator of cage induction motors. Recently, a linear parametric model of this…”
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Candidate gene regions and genetic heterogeneity in gluten sensitivity by Holopainen, P, Mustalahti, K, Uimari, P, Collin, P, Mäki, M, Partanen, J

“…BACKGROUND Gluten sensitivity is a common multifactorial disorder, manifested in the small intestine or on the skin as typical coeliac disease or dermatitis…”
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Effects of saturation on the forces in induction motors with whirling cage rotor by Tenhunen, A., Holopainen, T.P., Arkkio, A.

“…The effects of magnetic saturation on the radial magnetic forces in induction machines when the rotor is performing a cylindrical circular whirling motion are…”
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Coeliac Disease among Healthy Members of Multiple Case Coeliac Disease Families by Mustalahti, K., Sulkanen, S., Holopainen, P., Laurila, K., Collin, P., Partanen, J., Mäki, M.

“…Background: The main objective of the study was to assess the frequency of undetected coeliac disease among the first-degree relatives of families with two or…”
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Unbalanced magnetic pull induced by arbitrary eccentric motion of cage rotor in transient operation. Part 1: Analytical model by Holopainen, T. P., Tenhunen, A., Lantto, E., Arkkio, A.

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How to Ensure Low Vibration of 2-Pole Motors on Flexible Foundation: Copyright Material IEEE, Paper No. PCIC-2018-28 by Holopainen, Timo P., Roivainen, Janne, Aarnivuo, Samu

“…Motor vibrations are tested as a part of Factory Acceptance Testing (FAT), normally on a massive foundation. In 2-pole motors there are two main sources of…”
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Use of Closely Related Affected Individuals for the Genetic Study of Complex Diseases in Founder Populations by Bourgain, C., Génin, E., Holopainen, P., Mustalahti, K., Mäki, M., Partanen, J., Clerget-Darpoux, F.

“…We propose a method, the maximum identity length contrast (MILC) statistic, to locate genetic risk factors for complex diseases in founder populations. The…”
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Analysis of total rotor runout components with multi-probe roundness measurement method by Tiainen, T., Viitala, R., Holopainen, T.P., Hemming, B.

“…Several standards for vibration testing of rotating machinery define limits for relative shaft displacement during rotation. With requirements for relative…”
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Clinical associations of the risk alleles of HLA-cw6 and CCHCR1WWCC in psoriasis by SUOMELA, Sari, KAINU, Kati, REUNALA, Timo, KIVEKÄS, Kristiina, JANSEN, Christer, HOLOPAINEN, Päivi, ELOMAA, Outi, KERE, Juha, SAARIALHO-KERE, Ulpu, ONKAMO, Päivi, TIALA, Inkeri, HIMBERG, Johan, KOSKINEN, Lotta, SNELLMAN, Erna, KARVONEN, Seija-Liisa, KARVONEN, Jaakko, UURASMAA, Tutta

“…The PSORS1 locus is the consistently replicated genetic risk factor for psoriasis. Clinical associations with the main marker allele of PSORS1, HLA-Cw6, have…”
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Finite element free vibration analysis of eccentrically stiffened plates by Holopainen, T.P.

“…A new finite element model is proposed for free vibration analysis of eccentrically stiffened plates. The formulation allows the placement of any number of…”
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Genetic dissection between coeliac disease and dermatitis herpetiformis in sib pairs by KARELL, K., KORPONAY‐SZABO, I., SZALAI, Zs, HOLOPAINEN, P., MUSTALAHTI, K., COLLIN, P., MÄKI, M., PARTANEN, J.

“…Gluten sensitive enteropathy has various manifestations, of which the two major forms are classical coeliac disease (cCD) and dermatitis herpetiformis (DH). In…”
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Genetic dissection between silent and clinically diagnosed symptomatic forms of coeliac disease in multiplex families by Mustalahti, K., Holopainen, P., Karell, K., Mäki, M., Partanen, J.

“…Background. Coeliac disease has a large variation in clinical outcome. In addition to the classical disease with malabsorption, many individuals have a silent…”
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Not all HLA DR3 DQ2 Haplotypes Confer Equal Susceptibility to Coeliac Disease: Transmission Analysis in Families by Karell, K., Holopainen, P., Mustalahti, K., Collin, P., Mäki, M., Partanen, J.

“…Background: HLA-DQ is the only established susceptibility factor for coeliac disease. We tested whether all HLA haplotypes with the known risk marker, HLA-DQ2,…”
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Candidate gene region 15q26 and genetic susceptibility to coeliac disease in finnish families by SUSI, M, HOLOPAINEN, P, MUSTALAHTI, K, MÄKI, M, PARTANEN, J

“…Studies in the Irish and British populations have indicated that chromosome region 15q26 could include a novel non-HLA-linked locus conferring genetic…”
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Candidate Gene Region 15q26 and Genetic Susceptibility to Coeliac Disease in Finnish Families by M. Susi, P. Holopainen, K. Mustalahti, M. Mäki, J. Partanen

“…Background: Studies in the Irish and British populations have indicated that chromosome region 15q26 could include a novel non-HLA-linked locus conferring…”
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Single founder mutation (W380G) in type II protein C deficiency in Finland by Levo, A, Kuismanen, K, Holopainen, P, Vahtera, E, Rasi, V, Krusius, T, Partanen, J

“…The present study investigated the genetic basis for type II protein C deficiency in Finland, where this form has an unusually high incidence. We demonstrated…”
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