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BRUCE BOWLING, MD
MD
Family Medicine Physician
NPI: 1407881832IndividualAccepts Medicare
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
116545(NY)
CMS Specialties
PrimaryFAMILY PRACTICE
Education
STATE UNIVERSITY OF NEW YORK AT BUFFALO SCHOOL OF MEDICINE
Class of 1972
Research & Publications (18)
Inhibition of mitochondrial protein translation sensitizes melanoma cells to arsenic trioxide cytotoxicity via a reactive oxygen species dependent mechanism.
PMID 18297286·Cancer Chemother Pharmacol·2008
4-observational
Enhancement of arsenic trioxide cytotoxicity by dietary isothiocyanates in human leukemic cells via a reactive oxygen species-dependent mechanism.
PMID 19540589·Leuk Res·2010
8-other
High school biology/life science teachers' presentation of genetic counseling and health care career options in their classrooms.
PMID 19418210·J Genet Couns·2009
8-other
Routine reduction of glaucoma medication following phacoemulsification.
PMID 19251121·J Cataract Refract Surg·2009
8-other
Exclusion of homozygous PLCE1 (NPHS3) mutations in 69 families with idiopathic and hereditary FSGS.
PMID 18975016·Pediatr Nephrol·2009
8-other
Phenotype associated with the H626P mutation and other changes in the TGFBI gene in Czech families.
PMID 18259096·Ophthalmic Res·2008
5-case
Development and evaluation of a genetics literacy assessment instrument for undergraduates.
PMID 18202354·Genetics·2008
8-other
Distribution and diversity of russian wheat aphid (Hemiptera: Aphididae) biotypes in North America.
PMID 17972648·J Econ Entomol·2007
7-preclinical
Characterization of human genetics courses for nonbiology majors in U.S. colleges and universities.
PMID 17785405·CBE Life Sci Educ·2007
8-other
Macular corneal dystrophy types I and II are caused by distinct mutations in the CHST6 gene in Iceland.
PMID 17093400·Mol Vis·2006
8-other
Six2 is required for suppression of nephrogenesis and progenitor renewal in the developing kidney.
PMID 17036046·EMBO J·2006
7-preclinical
CHST6 mutations in North American subjects with macular corneal dystrophy: a comprehensive molecular genetic review.
PMID 16568029·Mol Vis·2006
8-other
Functional interactions between the Epstein-Barr virus BZLF1 protein and the promyelocytic leukemia protein.
PMID 16307818·Virus Res·2006
8-other
Outcomes of referrals by community optometrists to a hospital glaucoma service.
PMID 16113358·Br J Ophthalmol·2005
8-other
Vitreous wick syndrome--a potential cause of endophthalmitis after intravitreal injection of triamcinolone through the pars plana.
PMID 15183823·Am J Ophthalmol·2004
8-other
Polymorphic corneal amyloidosis: a disorder due to a novel mutation in the transforming growth factor beta-induced (BIGH3) gene.
PMID 15177960·Ophthalmology·2004
8-other
Hyaluronidase allergy after peribulbar anesthesia with orbital inflammation.
PMID 15093662·J Cataract Refract Surg·2004
5-case
Self-regulation predictors of medication adherence among ethnically different pediatric patients with renal transplants.
PMID 11700330·J Pediatr Psychol·2001
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 415 HOOPER RD
ENDWELL, NY 13760 - Phone
- (607) 754-3863
Quick Facts
- NPI
- 1407881832
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 54
- Publications
- 18
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