Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Aino Luukkonen"'
Autor:
Minna K Karjalainen, Johanna M Huusko, Johanna Ulvila, Jenni Sotkasiira, Aino Luukkonen, Kari Teramo, Jevon Plunkett, Verneri Anttila, Aarno Palotie, Ritva Haataja, Louis J Muglia, Mikko Hallman
Publikováno v:
PLoS ONE, Vol 7, Iss 12, p e51378 (2012)
Preterm birth is the major cause of neonatal mortality and morbidity. In many cases, it has severe life-long consequences for the health and neurological development of the newborn child. More than 50% of all preterm births are spontaneous, and curre
Externí odkaz:
https://doaj.org/article/6340bf155ea741d78d83b3b96d7c8d15
Autor:
Ritva Haataja, Minna K Karjalainen, Aino Luukkonen, Kari Teramo, Hilkka Puttonen, Marja Ojaniemi, Teppo Varilo, Bimal P Chaudhari, Jevon Plunkett, Jeffrey C Murray, Steven A McCarroll, Leena Peltonen, Louis J Muglia, Aarno Palotie, Mikko Hallman
Publikováno v:
PLoS Genetics, Vol 7, Iss 2, p e1001293 (2011)
Preterm birth is the major cause of neonatal death and serious morbidity. Most preterm births are due to spontaneous onset of labor without a known cause or effective prevention. Both maternal and fetal genomes influence the predisposition to spontan
Externí odkaz:
https://doaj.org/article/e7b39d52104847748ac6818679689356
Autor:
Anu Tuohimaa, Ritva Haataja, Aino Luukkonen, Mikko Hallman, Minna K. Karjalainen, Johanna M. Huusko
Publikováno v:
Pediatric Research. 71:93-99
Preterm birth is the major cause of mortality and morbidity in neonates. Intrauterine infection and/or inflammatory response are evident in 60–70% of spontaneous preterm births (SPTBs). Genetic factors significantly increase this risk. However, the
Autor:
Michelle Trusgnich, Hilkka Puttonen, Vineta Fellman, Aino Luukkonen, Tammy Shen, E. Warwick Daw, Mary F. Feitosa, Ingrid B. Borecki, Adrienne E.D. Stormo, Lisanne Palomar, Leena Peltonen, Kari Teramo, Ping An, Mikko Hallman, Jevon Plunkett, Zachary A.-F. Kistka, Emily DeFranco, Ritva Haataja, Aarno Palotie, Michael F. Wangler, Louis J. Muglia
Publikováno v:
Human Heredity. 68:209-219
Objective: While multiple lines of evidence suggest the importance of genetic contributors to risk of preterm birth, the nature of the genetic component has not been identified. We perform segregation analyses to identify the best fitting genetic mod
Autor:
Aino Luukkonen, Jeffrey C. Murray, Aarno Palotie, Ritva Haataja, Mikko Hallman, Minna K. Karjalainen, Teppo Varilo, Hilkka Puttonen, Jevon Plunkett, Kari Teramo, Leena Peltonen, Bimal P. Chaudhari, Steven A. McCarroll, Marja Ojaniemi, Louis J. Muglia
Publikováno v:
PLoS
PLoS Genetics
PLoS Genetics, Vol 7, Iss 2, p e1001293 (2011)
PLoS Genetics
PLoS Genetics, Vol 7, Iss 2, p e1001293 (2011)
Preterm birth is the major cause of neonatal death and serious morbidity. Most preterm births are due to spontaneous onset of labor without a known cause or effective prevention. Both maternal and fetal genomes influence the predisposition to spontan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a46352406dfbc9883e220e47f85ca7c8
http://hdl.handle.net/1721.1/64462
http://hdl.handle.net/1721.1/64462
Autor:
Annamari Salminen, Marja Ojaniemi, Anu Tuohimaa, Aino Luukkonen, Reija Paananen, Mikko Hallman, Stephan W. Glasser, Pentti Jouppila, Minna K. Karjalainen, Reetta Vuolteenaho, Ritva Haataja
Publikováno v:
Annals of medicine. 41(8)
Surfactant protein (SP) C has been shown to be expressed also outside pulmonary alveoli. Certain SP-C gene (SFTPC) polymorphisms associate with lung diseases and very preterm birth.We investigated the association of SFTPC single nucleotide polymorphi
Autor:
M Hallman, Louis J. Muglia, Ritva Haataja, Aarno Palotie, Aino Luukkonen, Minna K. Karjalainen, Johanna M. Huusko, J Sotkasiira, Johanna Ulvila
Publikováno v:
Pediatric Research. 70:659-659
Background: Preterm birth accounts for 2-3 million annual deaths worldwide and is the major cause of acute and chronic morbidity in children. More than 50% of preterm births have a spontaneous onset. Family studies suggest that genetic factors affect
Autor:
M. Adela Mansilla, Deb K. Pal, Thomas F. Wienker, Margaret E. Cooper, Kari Teramo, L. Leigh Field, Vineta Fellman, Peter Kraft, Yu-Chun Yen, Adrienne E.D. Stormo, Regina Zimmerman, Toby Goldstein McHenry, Têmis Maria Félix, Michelle Trusgnich, Tammy Shen, Lina Morene, Emily DeFranco, Sandra Daack-Hirsch, Hilkka Puttonen, Habibul Ahsan, Aarno Palotie, Astanand Jugessur, E. Warwick Daw, Kim Doheny, Donna Spiegelman, Andrew C. Lidral, Xiaoyi Gao, Aino Luukkonen, Manika Govil, Jeffrey C. Murray, Zachary A.-F. Kistka, Ingrid B. Borecki, Adrienne Tin, Michael F. Wangler, Sara Lindström, Alexandre R. Vieira, Eden R. Martin, Mary F. Feitosa, Consuelo Valencia-Ramirez, Mauricio Arcos-Burgos, Christine Fischer, Jevon Plunkett, Ritva Haataja, Brion S. Maher, Louis J. Muglia, Mary L. Marazita, Antonia Flaquer, Ping An, David A. Greenberg, Leena Peltonen, Bridget M. Riley, Elizabeth W. Pugh, Lisanne Palomar, Mikko Hallman
Publikováno v:
Human Heredity. 68:221-221