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The Pharmacogenomics Journal|December 18, 2013
SCN1A variations and response to multiple antiepileptic drugsT S C Yip, C O'Doherty, N C K Tan, et al.
The Pharmacogenomics Journal|March 22, 2021
CYP2D6 genotype and reduced codeine analgesic effect in real-world clinical practiceDaniel Carranza-Leon, Alyson L Dickson, Andrea Gaedigk, et al.
The Pharmacogenomics Journal|November 14, 2021
PIK3R5 genetic predictors of hypertension induced by VEGF-pathway inhibitorsJulia C F Quintanilha, Alessandro Racioppi, Jin Wang, et al.
The Pharmacogenomics Journal|November 6, 2021
Application of long-read sequencing to elucidate complex pharmacogenomic regions: a proof of principleMaaike van der Lee, William J Rowell, Roberta Menafra, et al.
The Pharmacogenomics Journal|March 13, 2021
Increased expression of IFI16 predicts adverse prognosis in multiple myelomaWenhui Huang, Tingting Qian, Zeyong Huang, et al.
The Pharmacogenomics Journal|March 2, 2021
The association between missense polymorphisms in SRD5A2 and HSD3B1 and treatment failure with abiraterone for castration-resistant prostate cancerMasaki Shiota, Shusuke Akamatsu, Shintaro Narita, et al.
The Pharmacogenomics Journal|October 23, 2022
Meta-analysis of pharmacogenetic clinical decision support systems for the treatment of major depressive disorderValentin Skryabin, Ilya Rozochkin, Mikhail Zastrozhin, et al.
The Pharmacogenomics Journal|June 3, 2020
Influence of genetic variants and antiepileptic drug co-treatment on lamotrigine plasma concentration in Mexican Mestizo patients with epilepsyAlberto Ortega-Vázquez, Ingrid Fricke-Galindo, Pedro Dorado, et al.
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