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JOHN BATEMAN, M.D.
M.D.
Emergency Medicine Physician
NPI: 1831369966Individual
Specialties, Licenses & Credentials
Emergency Medicine PhysicianPrimary
Emergency Medicine
Code: 207P00000X
4301088177(MI)
Research & Publications (20)
Genetic diseases of connective tissues: cellular and extracellular effects of ECM mutations.
PMID 19204719·Nat Rev Genet·2009
6-review
Gene conversion mutation in crystallin, beta-B2 (CRYBB2) in a Chilean family with autosomal dominant cataract.
PMID 17234267·Ophthalmology·2007
8-other
A new locus for autosomal dominant cataract on chromosome 19: linkage analyses and screening of candidate genes.
PMID 16877414·Invest Ophthalmol Vis Sci·2006
8-other
Identification of four novel COL10A1 missense mutations in schmid metaphyseal chondrodysplasia: further evidence that collagen X NC1 mutations impair trimer assembly.
PMID 15024737·Hum Mutat·2004
8-other
Tissue-specific RNA surveillance? Nonsense-mediated mRNA decay causes collagen X haploinsufficiency in Schmid metaphyseal chondrodysplasia cartilage.
PMID 12554676·Hum Mol Genet·2003
8-other
Mutational bisection of the mitochondrial DNA stability and amino acid biosynthetic functions of ilv5p of budding yeast.
PMID 12136009·Genetics·2002
8-other
Mitochondrial DNA instability mutants of the bifunctional protein Ilv5p have altered organization in mitochondria and are targeted for degradation by Hsp78 and the Pim1p protease.
PMID 12381727·J Biol Chem·2002
8-other
The molecular genetics of inherited cartilage disease.
PMID 11680678·Osteoarthritis Cartilage·2001
6-review
A new locus for autosomal dominant cataract on chromosome 12q13.
PMID 10937580·Invest Ophthalmol Vis Sci·2000
8-other
The effect of beam time structure on counting detectors in SRS experiments.
PMID 16609213·J Synchrotron Radiat·2000
8-other
Deficiency of annexins A5 and A6 induces complex changes in the transcriptome of growth plate cartilage but does not inhibit the induction of mineralization.
PMID 19580468·J Bone Miner Res·2010
7-preclinical
Mice lacking the extracellular matrix protein WARP develop normally but have compromised peripheral nerve structure and function.
PMID 19279005·J Biol Chem·2009
7-preclinical
The conserved translocase Tim17 prevents mitochondrial DNA loss.
PMID 18826960·Hum Mol Genet·2009
8-other
Duane retraction syndrome, nystagmus, retinal pigment epitheliopathy and epiretinal membrane with micro- and pachygyria, developmental delay, hearing loss and craniopharyngioma.
PMID 19172504·Ophthalmic Genet·2009
5-case
Portal vein thrombosis in the district general hospital: management and clinical outcomes.
PMID 19262399·Eur J Gastroenterol Hepatol·2009
4-observational
Global comparative transcriptome analysis of cartilage formation in vivo.
PMID 19272164·BMC Dev Biol·2009
7-preclinical
Employing molecular genetics of chondrodysplasias to inform the study of osteoarthritis.
PMID 19180483·Arthritis Rheum·2009
6-review
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 348 E 4500 S STE 220
MURRAY, UT 84107 - Phone
- (801) 577-7055
Quick Facts
- NPI
- 1831369966
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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