Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Bronchopulmonary Dysplasia and CRP[original query] |
---|
Exome sequencing and pathway analysis for identification of genetic variability relevant for bronchopulmonary dysplasia (BPD) in preterm newborns: A pilot study. Clinica chimica acta; international journal of clinical chemistry 2015 Jan . Carrera Paola, Di Resta Chiara, Volonteri Chiara, Castiglioni Emanuela, Bonfiglio Silvia, Lazarevic Dejan, Cittaro Davide, Stupka Elia, Ferrari Maurizio, Somaschini Marco, |
Genome-wide association study of bronchopulmonary dysplasia: a potential role for variants near the CRP gene. Scientific reports 2017 Aug 7 (1): 9271. Mahlman Mari, Karjalainen Minna K, Huusko Johanna M, Andersson Sture, Kari M Anneli, Tammela Outi K T, Sankilampi Ulla, Lehtonen Liisa, Marttila Riitta H, Bassler Dirk, Poets Christian F, Lacaze-Masmonteil Thierry, Danan Claude, Delacourt Christophe, Palotie Aarno, Muglia Louis J, Lavoie Pascal M, Hadchouel Alice, Rämet Mika, Hallman Mik |
Verification of immunology-related genetic associations in BPD supports ABCA3 and five other genes. Pediatric research 2021 9 92 (1): 190-198. Blume Felix, Kirsten Holger, Ahnert Peter, Chakraborty Trinad, Gross Arnd, Horn Katrin, Toliat Mohammad Reza, Nürnberg Peter, Westenfelder Eva-Maria, Goepel Wolfgang, Scholz Mark |
- Page last reviewed:Feb 1, 2024
- Content source: