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WILLIAM COLE, M.D.
M.D.
Family Medicine Physician
NPI: 1346229820IndividualAccepts Medicare
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
C-8112(AR)
Education
UNIVERSITY OF ARKANSAS COLLEGE OF MEDICINE
Class of 1991
Research & Publications (20)
Path-averaged Cn2 estimation using a laser-and-corner-cube system.
PMID 19623240·Appl Opt·2009
8-other
Identification and functional characterization of protein kinase A-catalyzed phosphorylation of potassium channel Kv1.2 at serine 449.
PMID 19389710·J Biol Chem·2009
7-preclinical
A review of family intervention guidelines for pediatric acquired brain injuries.
PMID 19489087·Dev Disabil Res Rev·2009
6-review
Age-related changes in motor subtle signs among girls and boys with ADHD.
PMID 18981373·Neurology·2008
8-other
Olpadronate reduced fractures in children with osteogenesis imperfecta.
PMID 15523042·J Bone Joint Surg Am·2004
8-other
ATP-sensitive K+ channels of vascular smooth muscle cells.
PMID 12625619·J Cardiovasc Electrophysiol·2003
6-review
Skeletal dysplasias reveal genes of importance in skeletal development and structure.
PMID 12952205·Connect Tissue Res·2003
7-preclinical
Inhibition by protein kinase C of the K(NDP) subtype of vascular smooth muscle ATP-sensitive potassium channel.
PMID 10903994·Circ Res·2000
7-preclinical
Low density lipoprotein receptor-related protein 5 (LRP5) mutations and osteoporosis, impaired glucose metabolism and hypercholesterolaemia.
PMID 19673927·Clin Endocrinol (Oxf)·2010
8-other
Ca2+ sensitization via phosphorylation of myosin phosphatase targeting subunit at threonine-855 by Rho kinase contributes to the arterial myogenic response.
PMID 19359365·J Physiol·2009
7-preclinical
ATP-sensitive K+ channels in pig urethral smooth muscle cells are heteromultimers of Kir6.1 and Kir6.2.
PMID 18945825·Am J Physiol Renal Physiol·2009
7-preclinical
Early-onset osteoarthritis due to otospondylomegaepiphyseal dysplasia in a family with a novel splicing mutation of the COL11A2 gene.
PMID 18381781·J Rheumatol·2008
5-case
Demonstration of the interaction of transforming growth factor beta 2 and type X collagen using a modified tandem affinity purification tag.
PMID 18952512·J Chromatogr B Analyt Technol Biomed Life Sci·2008
7-preclinical
Absence of apparent disease causing mutations in COL5A3 in 13 patients with hypermobility Ehlers-Danlos syndrome.
PMID 19012342·Am J Med Genet A·2008
8-other
Prevalence of aggressive behaviour after severe paediatric traumatic brain injury.
PMID 19005885·Brain Inj·2008
8-other
Shwachman-Diamond syndrome is associated with low-turnover osteoporosis.
PMID 17920346·Bone·2007
8-other
Transient receptor potential channel 6-mediated, localized cytosolic [Na+] transients drive Na+/Ca2+ exchanger-mediated Ca2+ entry in purinergically stimulated aorta smooth muscle cells.
PMID 17872462·Circ Res·2007
7-preclinical
COL10A1 nonsense and frame-shift mutations have a gain-of-function effect on the growth plate in human and mouse metaphyseal chondrodysplasia type Schmid.
PMID 17403716·Hum Mol Genet·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
- 100 HOLLYWOOD AVE
HOT SPRINGS, AR 71901 - Phone
- (501) 321-9292
Quick Facts
- NPI
- 1346229820
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 35
- Publications
- 20
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