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DANIEL EYRE, PHARMD
PHARMD
Pharmacist Clinician (PhC)/ Clinical Pharmacy Specialist
NPI: 1346484730Individual
Specialties, Licenses & Credentials
Pharmacist Clinician (PhC)/ Clinical Pharmacy SpecialistPrimary
Pharmacist — Pharmacist Clinician (PhC)/ Clinical Pharmacy Specialist
Code: 1835P0018X
6476725-1701(UT)
Research & Publications (20)
Differences in chain usage and cross-linking specificities of cartilage type V/XI collagen isoforms with age and tissue.
PMID 19103590·J Biol Chem·2009
7-preclinical
The Helix-II epitope: a cautionary tale from a cartilage biomarker based on an invalid collagen sequence.
PMID 19248751·Osteoarthritis Cartilage·2009
8-other
In Saccharomyces cerevisiae, yKu and subtelomeric core X sequences repress homologous recombination near telomeres as part of the same pathway.
PMID 19652177·Genetics·2009
8-other
Biochemical markers of bone turnover and their association with bone marrow lesions.
PMID 18759975·Arthritis Res Ther·2008
8-other
The heterozygous disproportionate micromelia (dmm) mouse: morphological changes in fetal cartilage precede postnatal dwarfism and compared with lethal homozygotes can explain the mild phenotype.
PMID 18678883·J Histochem Cytochem·2008
4-observational
Using biochemical markers of bone turnover in clinical practice.
PMID 18939390·Cleve Clin J Med·2008
6-review
Spondylocheiro dysplastic form of the Ehlers-Danlos syndrome--an autosomal-recessive entity caused by mutations in the zinc transporter gene SLC39A13.
PMID 18513683·Am J Hum Genet·2008
5-case
The post-translational phenotype of collagen synthesized by SAOS-2 osteosarcoma cells.
PMID 17320498·Bone·2007
8-other
Genetic and constitutional influences on bone turnover markers: a study of male twin pairs.
PMID 17308989·Calcif Tissue Int·2007
4-observational
Cartilage markers and their association with cartilage loss on magnetic resonance imaging in knee osteoarthritis: the Boston Osteoarthritis Knee Study.
PMID 17958892·Arthritis Res Ther·2007
4-observational
Collagen XI chain misassembly in cartilage of the chondrodysplasia (cho) mouse.
PMID 17683922·Matrix Biol·2007
7-preclinical
Prolyl 3-hydroxylase 1 deficiency causes a recessive metabolic bone disorder resembling lethal/severe osteogenesis imperfecta.
PMID 17277775·Nat Genet·2007
5-case
Urinary levels of type II collagen C-telopeptide crosslink are unrelated to joint space narrowing in patients with knee osteoarthritis.
PMID 16339292·Ann Rheum Dis·2006
8-other
Sp1 family of transcription factors regulates the human alpha2 (XI) collagen gene (COL11A2) in Saos-2 osteoblastic cells.
PMID 16734381·J Bone Miner Res·2006
8-other
The predictive role of bone turnover markers for BMD in middle-aged men.
PMID 16916744·Aging Male·2006
8-other
CRTAP is required for prolyl 3- hydroxylation and mutations cause recessive osteogenesis imperfecta.
PMID 17055431·Cell·2006
7-preclinical
Deficiency of cartilage-associated protein in recessive lethal osteogenesis imperfecta.
PMID 17192541·N Engl J Med·2006
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 2121 NORTH AVE
GRAND JUNCTION, CO 81501 - Phone
- (970) 263-2800
Quick Facts
- NPI
- 1346484730
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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