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ASHTON BEGGS, PHARMD
PHARMD
Pharmacist
NPI: 1376041897Individual
Specialties, Licenses & Credentials
PharmacistPrimary
Pharmacist
Code: 183500000X
26023726A(IN)36926(TN)
Research & Publications (20)
A pilot study of ultrasound guided Durasphere injection in the treatment of faecal incontinence.
PMID 19438887·Colorectal Dis·2010
8-other
Genomics and breast cancer: the different levels of inherited susceptibility.
PMID 19092772·Eur J Hum Genet·2009
8-other
The exon 55 deletion in the nebulin gene--one single founder mutation with world-wide occurrence.
PMID 19232495·Neuromuscul Disord·2009
8-other
Fast-twitch sarcomeric and glycolytic enzyme protein loss in inclusion body myositis.
PMID 19291799·Muscle Nerve·2009
8-other
Thin filament length dysregulation contributes to muscle weakness in nemaline myopathy patients with nebulin deficiency.
PMID 19346529·Hum Mol Genet·2009
7-preclinical
Mutations and polymorphisms of the skeletal muscle alpha-actin gene (ACTA1).
PMID 19562689·Hum Mutat·2009
8-other
Abnormalities of the large ribosomal subunit protein, Rpl35a, in Diamond-Blackfan anemia.
PMID 18535205·Blood·2008
5-case
Dynamic regulation of endothelial NOS mediated by competitive interaction with alpha-actinin-4 and calmodulin.
PMID 18180332·FASEB J·2008
7-preclinical
Acute appendicitis is characterized by a uniform and highly selective pattern of inflammatory gene expression.
PMID 19079191·Mucosal Immunol·2008
8-other
The DCC gene and colorectal cancer: the story is more complex.
PMID 18266884·Colorectal Dis·2008
8-other
Ribosomal protein L5 and L11 mutations are associated with cleft palate and abnormal thumbs in Diamond-Blackfan anemia patients.
PMID 19061985·Am J Hum Genet·2008
8-other
AAV-mediated intramuscular delivery of myotubularin corrects the myotubular myopathy phenotype in targeted murine muscle and suggests a function in plasma membrane homeostasis.
PMID 18434328·Hum Mol Genet·2008
7-preclinical
Myofiber size correlates with MTM1 mutation type and outcome in X-linked myotubular myopathy.
PMID 17537630·Neuromuscul Disord·2007
8-other
Type I interferon-inducible gene expression in blood is present and reflects disease activity in dermatomyositis and polymyositis.
PMID 17968926·Arthritis Rheum·2007
8-other
Distinctive patterns of microRNA expression in primary muscular disorders.
PMID 17942673·Proc Natl Acad Sci U S A·2007
8-other
Nemaline myopathy with minicores caused by mutation of the CFL2 gene encoding the skeletal muscle actin-binding protein, cofilin-2.
PMID 17160903·Am J Hum Genet·2007
8-other
Selenoproteins and their impact on human health through diverse physiological pathways.
PMID 16990451·Physiology (Bethesda)·2006
6-review
Skeletal muscle repair in a mouse model of nemaline myopathy.
PMID 16877500·Hum Mol Genet·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
- 1900 BELMONT BLVD
NASHVILLE, TN 37212 - Phone
- (615) 460-6744
Quick Facts
- NPI
- 1376041897
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 20
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