Associated Papers
Novel Loss-of-Function Mutations in NPR2 Cause Acromesomelic Dysplasia, Maroteaux Type.
Wu J et al.
Frontiers in Genetics, 2022
35368703 (PubMed )
Supplement: DataSheet1.zip › 823861_SupMaterial › Data_Sheet_1.ZIP › raw_datas › patient_2__NGS_raw_data.xlsx › Sheet1
Genetic variants in cellular transport do not affect mesalamine response in ulcerative colitis.
Moran CJ et al.
Plos One, 2018
Recent advance in the pharmacogenomics of human Solute Carrier Transporters (SLCs) in drug disposition.
Zhou F et al.
Advanced Drug Delivery Reviews, 2017
Characterization of SLCO5A1/OATP5A1, a solute carrier transport protein with non-classical function.
Sebastian K et al.
Plos One, 2013
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