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JACOB TEAGUE, PHARMD
PHARMD
Pharmacist
NPI: 1851911481Individual
Specialties, Licenses & Credentials
PharmacistPrimary
Pharmacist
Code: 183500000X
41408(TN)
Research & Publications (20)
SNS-314, a pan-Aurora kinase inhibitor, shows potent anti-tumor activity and dosing flexibility in vivo.
PMID 19649632·Cancer Chemother Pharmacol·2010
7-preclinical
Somatic mutation databases as tools for molecular epidemiology and molecular pathology of cancer: proposed guidelines for improving data collection, distribution, and integration.
PMID 19006239·Hum Mutat·2009
8-other
A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation.
PMID 19377476·Nat Genet·2009
8-other
Somatic mutations of the histone H3K27 demethylase gene UTX in human cancer.
PMID 19330029·Nat Genet·2009
8-other
Discovery of a potent and selective aurora kinase inhibitor.
PMID 18678489·Bioorg Med Chem Lett·2008
7-preclinical
SLC9A6 mutations cause X-linked mental retardation, microcephaly, epilepsy, and ataxia, a phenotype mimicking Angelman syndrome.
PMID 18342287·Am J Hum Genet·2008
8-other
An endogenous prostaglandin enhances environmental phthalate-induced apoptosis in bone marrow B cells: activation of distinct but overlapping pathways.
PMID 18641309·J Immunol·2008
7-preclinical
The Catalogue of Somatic Mutations in Cancer (COSMIC).
PMID 18428421·Curr Protoc Hum Genet·2008
8-other
Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing.
PMID 18438408·Nat Genet·2008
8-other
Oligosaccharyltransferase-subunit mutations in nonsyndromic mental retardation.
PMID 18455129·Am J Hum Genet·2008
8-other
X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment.
PMID 18469813·Nat Genet·2008
4-observational
Mutations in the BRWD3 gene cause X-linked mental retardation associated with macrocephaly.
PMID 17668385·Am J Hum Genet·2007
5-case
Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation.
PMID 17704778·Nat Genet·2007
8-other
Mutations in CUL4B, which encodes a ubiquitin E3 ligase subunit, cause an X-linked mental retardation syndrome associated with aggressive outbursts, seizures, relative macrocephaly, central obesity, hypogonadism, pes cavus, and tremor.
PMID 17236139·Am J Hum Genet·2007
8-other
The original Lujan syndrome family has a novel missense mutation (p.N1007S) in the MED12 gene.
PMID 17369503·J Med Genet·2007
4-observational
Mutations in ZDHHC9, which encodes a palmitoyltransferase of NRAS and HRAS, cause X-linked mental retardation associated with a Marfanoid habitus.
PMID 17436253·Am J Hum Genet·2007
5-case
AutoCSA, an algorithm for high throughput DNA sequence variant detection in cancer genomes.
PMID 17485433·Bioinformatics·2007
8-other
An assessment of the in vivo efficacy of the glycogen phosphorylase inhibitor GPi688 in rat models of hyperglycaemia.
PMID 17934512·Br J Pharmacol·2007
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
- 2500 LEBANON PIKE
NASHVILLE, TN 37214 - Phone
- (615) 889-6300
Quick Facts
- NPI
- 1851911481
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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