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TRAYLOR MOSES, PHARMD
PHARMD
Pharmacist
NPI: 1265313050Individual
Specialties, Licenses & Credentials
PharmacistPrimary
Pharmacist
Code: 183500000X
231230-40(WI)
Research & Publications (20)
Stigma and self-concept among adolescents receiving mental health treatment.
PMID 19485644·Am J Orthopsychiatry·2009
8-other
Self-labeling and its effects among adolescents diagnosed with mental disorders.
PMID 19084313·Soc Sci Med·2009
8-other
Social workers' attitudes about psychotropic drug treatment with youths.
PMID 17076119·Soc Work·2006
8-other
Does the clinical course of depression determine improvement in symptoms and quality of life?
PMID 16614544·J Nerv Ment Dis·2006
4-observational
TLR4-mediated Cox-2 expression increases intestinal ischemia/reperfusion-induced damage.
PMID 19564573·J Leukoc Biol·2009
7-preclinical
Iodine nutritional status of children on the island of Tanna, Republic of Vanuatu.
PMID 19152716·Public Health Nutr·2009
8-other
PI3K/AKT pathway activation in acute myeloid leukaemias is not associated with AKT1 pleckstrin homology domain mutation.
PMID 18053070·Br J Haematol·2008
8-other
Admixture and population stratification in African Caribbean populations.
PMID 17908263·Ann Hum Genet·2008
8-other
A transforming mutation in the pleckstrin homology domain of AKT1 in cancer.
PMID 17611497·Nature·2007
7-preclinical
Genome-wide linkage of 77 families from the African American Hereditary Prostate Cancer study (AAHPC).
PMID 17031815·Prostate·2007
4-observational
A cybernetic model to predict the effect of freely available nitrogen substrate on rifamycin B production in complex media.
PMID 16534611·Appl Microbiol Biotechnol·2006
8-other
A common nonsense mutation in EphB2 is associated with prostate cancer risk in African American men with a positive family history.
PMID 16155194·J Med Genet·2006
8-other
Nonsense-mediated decay microarray analysis identifies mutations of EPHB2 in human prostate cancer.
PMID 15300251·Nat Genet·2004
8-other
Cloning and characterization of a novel gene, SHPRH, encoding a conserved putative protein with SNF2/helicase and PHD-finger domains from the 6q24 region.
PMID 12837266·Genomics·2003
7-preclinical
Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome.
PMID 12714972·Nature·2003
8-other
HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome.
PMID 12434154·Nat Genet·2002
8-other
Germline mutations in the ribonuclease L gene in families showing linkage with HPC1.
PMID 11799394·Nat Genet·2002
8-other
Surface ordering above the isotropic-smectic-A transition at a silane-treated substrate.
PMID 11461211·Phys Rev E Stat Nonlin Soft Matter Phys·2001
8-other
Evaluation of linkage and association of HPC2/ELAC2 in patients with familial or sporadic prostate cancer.
PMID 11254448·Am J Hum Genet·2001
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 2900 W OKLAHOMA AVE
MILWAUKEE, WI 53215 - Phone
- (414) 649-6000
Quick Facts
- NPI
- 1265313050
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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