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Genome-wide association study of bronchopulmonary dysplasia: a potential role for variants near the CRP gene.
Mahlman M, Karjalainen MK, Huusko JM, Andersson S, Kari MA, Tammela OKT, Sankilampi U, Lehtonen L, Marttila RH, Bassler D, Poets CF, Lacaze-Masmonteil T, Danan C, Delacourt C, Palotie A, Muglia LJ, Lavoie PM, Hadchouel A, Rämet M, Hallman M. Mahlman M, et al. Among authors: huusko jm. Sci Rep. 2017 Aug 24;7(1):9271. doi: 10.1038/s41598-017-08977-w. Sci Rep. 2017. PMID: 28839172 Free PMC article.
Identification of SPOCK2 as a susceptibility gene for bronchopulmonary dysplasia.
Hadchouel A, Durrmeyer X, Bouzigon E, Incitti R, Huusko J, Jarreau PH, Lenclen R, Demenais F, Franco-Montoya ML, Layouni I, Patkai J, Bourbon J, Hallman M, Danan C, Delacourt C. Hadchouel A, et al. Among authors: huusko j. Am J Respir Crit Care Med. 2011 Nov 15;184(10):1164-70. doi: 10.1164/rccm.201103-0548OC. Epub 2011 Aug 11. Am J Respir Crit Care Med. 2011. PMID: 21836138 Free PMC article.
CXCR3 Polymorphism and Expression Associate with Spontaneous Preterm Birth.
Karjalainen MK, Ojaniemi M, Haapalainen AM, Mahlman M, Salminen A, Huusko JM, Määttä TA, Kaukola T, Anttonen J, Ulvila J, Haataja R, Teramo K, Kingsmore SF, Palotie A, Muglia LJ, Rämet M, Hallman M. Karjalainen MK, et al. Among authors: huusko jm. J Immunol. 2015 Sep 1;195(5):2187-98. doi: 10.4049/jimmunol.1501174. Epub 2015 Jul 24. J Immunol. 2015. PMID: 26209629
56 results