Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Nina Airla"'
Autor:
Mari Levula, Niku Oksala, Nina Airla, Rainer Zeitlin, Juha-Pekka Salenius, Otso Järvinen, Maarit Venermo, Teemu Partio, Jukka Saarinen, Taija Somppi, VeliPekka Suominen, Jyrki Virkkunen, Juha Hautalahti, Reijo Laaksonen, Mika Kähönen, Ari Mennander, Leena Kytömäki, Juhani T Soini, Jyrki Parkkinen, Markku Pelto-Huikko, Terho Lehtimäki
Publikováno v:
PLoS ONE, Vol 7, Iss 4, p e33787 (2012)
BACKGROUND: Atherosclerosis is a complex disease with hundreds of genes influencing its progression. In addition, the phenotype of the disease varies significantly depending on the arterial bed. METHODOLOGY/PRINCIPAL FINDINGS: We characterized the ge
Externí odkaz:
https://doaj.org/article/c59366f0fb374c6582592232ae32e3b3
Autor:
Terho Lehtimäki, Liisa Keltikangas-Järvinen, Helle Pullmann, Saija Alatupa, Jari Lipsanen, Nina Airla, Laura Pulkki-Råback
Publikováno v:
Mind, Brain, and Education. 2:104-110
— High parental socioeconomic status is known to have a positive effect on students’ academic achievement. We examined whether variation in the dopamine receptor gene (DRD2 polymorphism, rs 1800497) modifies the association between parental educa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::099cf11893ee544d06343257a6a1ddaf
https://doi.org/10.1111/j.1751-228x.2008.00038.x
https://doi.org/10.1111/j.1751-228x.2008.00038.x
Autor:
Juha-Pekka Salenius, Jyrki Virkkunen, Reijo Laaksonen, Leena Kytömäki, Niku Oksala, Rainer Zeitlin, Mari Levula, Velipekka Suominen, Markku Pelto-Huikko, Ari Mennander, Jyrki Parkkinen, Mika Kähönen, Maarit Venermo, Juha Hautalahti, Juhani T. Soini, Otso Järvinen, Taija Somppi, Teemu Partio, Nina Airla, Terho Lehtimäki, Jukka Saarinen
Publikováno v:
PLoS ONE, Vol 7, Iss 4, p e33787 (2012)
PLoS ONE
PLoS ONE; Vol 7
PLoS ONE
PLoS ONE; Vol 7
BACKGROUND: Atherosclerosis is a complex disease with hundreds of genes influencing its progression. In addition, the phenotype of the disease varies significantly depending on the arterial bed. METHODOLOGY/PRINCIPAL FINDINGS: We characterized the ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e49648fffe7334462a57d28d3e5204da
http://europepmc.org/articles/PMC3324479?pdf=render
http://europepmc.org/articles/PMC3324479?pdf=render
Autor:
Nihan Erginel-Unaltuna, Mika Kähönen, Juha-Pekka Salenius, Juhani T. Soini, Bilge Ozsait, Nina Airla, Reijo Laaksonen, Leena Kytömäki, Pekka J. Karhunen, Terho Lehtimäki, Otso Järvinen, Ari-Pekka J. Huovila, Mari Levula, Niku Oksala, Evrim Komurcu-Bayrak, Markku Pelto-Huikko, Rebekka M. Ortiz
Publikováno v:
Annals of Medicine; Vol 41
Annals of Medicine
Annals of Medicine
Background and aims. The expression of disintegrin and metalloprotease ADAM-9, ADAM-15, and ADAM-17 has been associated with cell-cell, cell-platelet, and cell-matrix interactions and inflammation. They are possibly implicated in the pathophysiology
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac669d9028381fdc1a7e99d33bb89e6d
https://pubmed.ncbi.nlm.nih.gov/19253070
https://pubmed.ncbi.nlm.nih.gov/19253070
Autor:
Laura Pulkki-Råback, Nina Airla, Markus Jokela, Mika Kivimäki, Liisa Keltikangas-Järvinen, Marko Elovainio, Terho Lehtimäki
Publikováno v:
Psychosomatic medicine. 69(5)
OBJECTIVE: To examine the potential moderating role of DRD2 polymorphism (rs1800497) in the association between stressful life events and depressive symptoms among young adults. Although stressful life events, such as divorce, unemployment, and serio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd91063b71393529a6b8a451acae7f26
https://pubmed.ncbi.nlm.nih.gov/17585060
https://pubmed.ncbi.nlm.nih.gov/17585060
Autor:
Terho Lehtimäki, Irina Elovaara, Markku Koskenvuo, Jaakko Kaprio, Mari Levula, Nina Airla, Raija Paalavuo, H. Kuusisto, Silja Särkijärvi
Publikováno v:
BMC Medical Genetics
BMC Medical Genetics, Vol 7, Iss 1, p 11 (2006)
BMC Medical Genetics, Vol 7, Iss 1, p 11 (2006)
Background Since genetic alterations influencing susceptibility to multiple sclerosis (MS), the most common autoimmune demyelinating disease of the central nervous system (CNS), are as yet poorly understood, the purpose of this study was to identify
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7d9f0166019001e6485ef0f8b63e508
http://europepmc.org/articles/PMC1421383
http://europepmc.org/articles/PMC1421383