Your browser doesn't support javascript.
loading
Functional assessment of genetic variants located in the promoter of SHP1 (NR0B2).
Prestin, Katharina; Olbert, Maria; Hussner, Janine; Völzke, Henry; Meyer Zu Schwabedissen, Henriette E.
Affiliation
  • Prestin K; aDepartment of Pharmaceutical Sciences, University of Basel, Basel, Switzerland bC_DAT Center of Drug Absorption and Transport; Institute of Pharmacology cInstitute for Community Medicine, University Medicine Greifswald, Greifswald, Germany.
Pharmacogenet Genomics ; 27(11): 410-415, 2017 Nov.
Article in En | MEDLINE | ID: mdl-28873070
Subject(s)
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Inactivation, Metabolic / Transcriptional Activation / Receptors, Cytoplasmic and Nuclear / Pharmacogenomic Variants Type of study: Observational_studies / Prognostic_studies Limits: Female / Humans / Male Language: En Journal: Pharmacogenet Genomics Journal subject: FARMACOLOGIA / GENETICA MEDICA Year: 2017 Document type: Article Affiliation country:
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Inactivation, Metabolic / Transcriptional Activation / Receptors, Cytoplasmic and Nuclear / Pharmacogenomic Variants Type of study: Observational_studies / Prognostic_studies Limits: Female / Humans / Male Language: En Journal: Pharmacogenet Genomics Journal subject: FARMACOLOGIA / GENETICA MEDICA Year: 2017 Document type: Article Affiliation country: