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SCOTT JOHNS, PHARM.D.
PHARM.D.
Pharmacotherapy Pharmacist
NPI: 1780696393Individual
Specialties, Licenses & Credentials
Pharmacotherapy PharmacistPrimary
Pharmacist — Pharmacotherapy
Code: 1835P1200X
RPH 40642(CA)
Research & Publications (20)
Foxn1 is required for tissue assembly and desmosomal cadherin expression in the hair shaft.
PMID 15739220·Dev Dyn·2005
7-preclinical
Subjective life expectancy predicts offspring sex in a contemporary British population.
PMID 15801608·Proc Biol Sci·2004
4-observational
Functional genetic variation in the basal promoter of the organic cation/carnitine transporters OCTN1 (SLC22A4) and OCTN2 (SLC22A5).
PMID 19141711·J Pharmacol Exp Ther·2009
8-other
Differences in tuberculin reactivity as determined in a veterans administration employee health screening program.
PMID 19225075·Clin Vaccine Immunol·2009
8-other
Genetic variants in multidrug and toxic compound extrusion-1, hMATE1, alter transport function.
PMID 19172157·Pharmacogenomics J·2009
8-other
Identification and characterization of proximal promoter polymorphisms in the human concentrative nucleoside transporter 2 (SLC28A2).
PMID 19098160·J Pharmacol Exp Ther·2009
7-preclinical
Characterization of ontogenetic changes in gene expression in the fathead minnow (Pimephales promelas).
PMID 19391683·Environ Toxicol Chem·2009
7-preclinical
The human multidrug resistance protein 4 (MRP4, ABCC4): functional analysis of a highly polymorphic gene.
PMID 18364470·J Pharmacol Exp Ther·2008
8-other
Randomized, double-blind, placebo-controlled crossover trials of venlafaxine for hot flashes after breast cancer.
PMID 17227907·Oncologist·2007
2-rct
Functional effects of protein sequence polymorphisms in the organic cation/ergothioneine transporter OCTN1 (SLC22A4).
PMID 17700366·Pharmacogenet Genomics·2007
8-other
PharmGKB submission update: IV. PMT submissions of genetic variations in ATP-Binding cassette transporters to the PharmGKB network.
PMID 16507877·Pharmacol Rev·2006
8-other
PharmGKB submission update: V. PMT submissions of genetic variation in SLC22 family transporters.
PMID 16507878·Pharmacol Rev·2006
8-other
Depletion of Aspergillus nidulans cotA causes a severe polarity defect which is not suppressed by the nuclear migration mutation nudA2.
PMID 16506053·Mol Genet Genomics·2006
8-other
PharmGKB submission update: VI. PMT submissions of genetic variations in neurotransmitter transporters (SLC6, SLC17, and SLC18) to the PharmGKB network.
PMID 16507879·Pharmacol Rev·2006
8-other
Functional characterization and haplotype analysis of polymorphisms in the human equilibrative nucleoside transporter, ENT2.
PMID 16214850·Drug Metab Dispos·2006
4-observational
The human organic anion transporter 3 (OAT3; SLC22A8): genetic variation and functional genomics.
PMID 16291576·Am J Physiol Renal Physiol·2006
8-other
The International Gene Trap Consortium Website: a portal to all publicly available gene trap cell lines in mouse.
PMID 16381950·Nucleic Acids Res·2006
7-preclinical
Graves disease: an increasingly recognized immune reconstitution syndrome.
PMID 16439886·AIDS·2006
5-case
Interaction of methotrexate with organic-anion transporting polypeptide 1A2 and its genetic variants.
PMID 16702441·J Pharmacol Exp Ther·2006
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 3350 LA JOLLA VILLAGE DR
SAN DIEGO, CA 92161 - Phone
- (858) 552-8585
Quick Facts
- NPI
- 1780696393
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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