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Identification of molecular signatures of cystic fibrosis disease status with plasma-based functional genomics

Although cystic fibrosis (CF) is attributed to dysfunction of a single gene, the relationships between the abnormal gene product and the development of inflammation and progression of lung disease are not fully understood, which limits our ability to predict an individual patient’s clinical course a...

Πλήρης περιγραφή

Αποθηκεύτηκε σε:
Λεπτομέρειες βιβλιογραφικής εγγραφής
Τόπος έκδοσης:Physiol Genomics
Κύριοι συγγραφείς: Levy, Hara, Jia, Shuang, Pan, Amy, Zhang, Xi, Kaldunski, Mary, Nugent, Melodee L., Reske, Melissa, Feliciano, Rachel A., Quintero, Diana, Renda, Michael M., Woods, Katherine J., Murkowski, Kathy, Johnson, Keven, Verbsky, James, Dasu, Trivikram, Ideozu, Justin Eze, McColley, Susanna, Quasney, Michael W., Dahmer, Mary K., Avner, Ellis, Farrell, Philip M., Cannon, Carolyn L., Jacob, Howard, Simpson, Pippa M., Hessner, Martin J.
Μορφή: Artigo
Γλώσσα:Inglês
Έκδοση: American Physiological Society 2019
Θέματα:
Διαθέσιμο Online:https://ncbi.nlm.nih.gov/pmc/articles/PMC6383551/
https://ncbi.nlm.nih.gov/pubmed/30540547
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/physiolgenomics.00109.2018
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