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SCOTT WILKIE, DO
DO
Neuromusculoskeletal Medicine & OMM Physician
NPI: 1811482433IndividualAccepts Medicare
Specialties, Licenses & Credentials
Neuromusculoskeletal Medicine & OMM PhysicianPrimary
Neuromusculoskeletal Medicine & OMM
Code: 204D00000X
5101024270(MI)
CMS Specialties
PrimaryOSTEOPATHIC MANIPULATIVE MEDICINE
Education
OTHER
Class of 2020
Research & Publications (20)
Retargeting of human T cells to tumor-associated MUC1: the evolution of a chimeric antigen receptor.
PMID 18354214·J Immunol·2008
8-other
Disease mechanism for retinitis pigmentosa (RP11) caused by missense mutations in the splicing factor gene PRPF31.
PMID 18431455·Mol Vis·2008
8-other
The molecular evolution of avian ultraviolet- and violet-sensitive visual pigments.
PMID 17556758·Mol Biol Evol·2007
7-preclinical
Genetic enhancement of cognition in a kindred with cone-rod dystrophy due to RIMS1 mutation.
PMID 17237123·J Med Genet·2007
3-trial
Vertebrate opsins belonging to different classes vary in constitutively active properties resulting from salt-bridge mutations.
PMID 16752919·Biochemistry·2006
7-preclinical
Shortwave visual sensitivity in tree and flying squirrels reflects changes in lifestyle.
PMID 16461266·Curr Biol·2006
4-observational
Mutations in the gene KCNV2 encoding a voltage-gated potassium channel subunit cause "cone dystrophy with supernormal rod electroretinogram" in humans.
PMID 16909397·Am J Hum Genet·2006
8-other
A study of the nuclear trafficking of the splicing factor protein PRPF31 linked to autosomal dominant retinitis pigmentosa (ADRP).
PMID 16427773·Biochim Biophys Acta·2006
7-preclinical
Mutation in the gene GUCA1A, encoding guanylate cyclase-activating protein 1, causes cone, cone-rod, and macular dystrophy.
PMID 15953638·Ophthalmology·2005
8-other
Effects of testosterone administration in human immunodeficiency virus-infected women with low weight: a randomized placebo-controlled study.
PMID 15111377·Arch Intern Med·2004
3-trial
Divergent mechanisms for the tuning of shortwave sensitive visual pigments in vertebrates.
PMID 15295625·Photochem Photobiol Sci·2004
6-review
Dominant cone and cone-rod dystrophies: functional analysis of mutations in retGC1 and GCAP1.
PMID 14750595·Novartis Found Symp·2004
8-other
Purification, characterisation and intracellular localisation of aryl hydrocarbon interacting protein-like 1 (AIPL1) and effects of mutations associated with inherited retinal dystrophies.
PMID 15469903·Biochim Biophys Acta·2004
7-preclinical
Dosing regimen and hematologic effects of pentoxifylline and its active metabolites in normal dogs.
PMID 14506595·Vet Ther·2003
3-trial
Genomic organisation and alternative splicing of human RIM1, a gene implicated in autosomal dominant cone-rod dystrophy (CORD7).
PMID 12659814·Genomics·2003
8-other
Neurocognitive function in HIV-infected patients with low weight and weight loss.
PMID 14526204·J Acquir Immune Defic Syndr·2003
8-other
Reduced testosterone levels in human immunodeficiency virus-infected women with weight loss and low weight.
PMID 12567309·Clin Infect Dis·2003
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
- 4660 S HAGADORN RD STE 500
EAST LANSING, MI 48823 - Phone
- (517) 432-6144
Quick Facts
- NPI
- 1811482433
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 6
- Publications
- 20
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