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ERIN LORAINE DEERY MD

MD

Internal Medicine Physician

NPI: 1477203834Individual

Specialties, Licenses & Credentials

Internal Medicine PhysicianPrimary

Internal Medicine

Code: 207R00000X

2025-00866(NC)
Student in an Organized Health Care Education/Training Program

Student in an Organized Health Care Education/Training Program

Code: 390200000X

Research & Publications (17)

Disease mechanism for retinitis pigmentosa (RP11) caused by mutations in the splicing factor gene PRPF31.
PMID 12444105·Hum Mol Genet·2002
4-observational
The AAA(+) motor complex of subunits CobS and CobT of cobaltochelatase visualized by single particle electron microscopy.
PMID 19545636·J Struct Biol·2009
8-other
Demonstration that CobG, the monooxygenase associated with the ring contraction process of the aerobic cobalamin (vitamin B12) biosynthetic pathway, contains an Fe-S center and a mononuclear non-heme iron center.
PMID 19068481·J Biol Chem·2009
8-other
Identification, characterization, and structure/function analysis of a corrin reductase involved in adenosylcobalamin biosynthesis.
PMID 18263579·J Biol Chem·2008
8-other
Biochemical and structural insights into bacterial organelle form and biogenesis.
PMID 18332146·J Biol Chem·2008
8-other
Elucidation of substrate specificity in the cobalamin (vitamin B12) biosynthetic methyltransferases. Structure and function of the C20 methyltransferase (CbiL) from Methanothermobacter thermautotrophicus.
PMID 17567575·J Biol Chem·2007
8-other
Aerobic synthesis of vitamin B12: ring contraction and cobalt chelation.
PMID 16042605·Biochem Soc Trans·2005
6-review
Anaerobic synthesis of vitamin B12: characterization of the early steps in the pathway.
PMID 16042604·Biochem Soc Trans·2005
6-review
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
Dominant cone and cone-rod dystrophies: functional analysis of mutations in retGC1 and GCAP1.
PMID 14750595·Novartis Found Symp·2004
8-other
Cobalamin synthesis in Yersinia enterocolitica 8081. Functional aspects of a putative metabolic island.
PMID 12756726·Adv Exp Med Biol·2003
8-other
Characterisation of two genes for guanylate cyclase activator protein (GCAP1 and GCAP2) in the Japanese pufferfish, Fugu rubripes.
PMID 12151097·Biochim Biophys Acta·2002
8-other
Cobalamin (vitamin B(12)) biosynthesis in Rhodobacter capsulatus.
PMID 12196155·Biochem Soc Trans·2002
8-other
Guanylate cyclase activating proteins, guanylate cyclase and disease.
PMID 12596936·Adv Exp Med Biol·2002
6-review
The destabilization of human GCAP1 by a proline to leucine mutation might cause cone-rod dystrophy.
PMID 11136713·Hum Mol Genet·2001
7-preclinical
Identification and functional consequences of a new mutation (E155G) in the gene for GCAP1 that causes autosomal dominant cone dystrophy.
PMID 11484154·Am J Hum Genet·2001
8-other
Functional characterization of missense mutations at codon 838 in retinal guanylate cyclase correlates with disease severity in patients with autosomal dominant cone-rod dystrophy.
PMID 11115851·Hum Mol Genet·2000
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
2295 E 14TH ST STE 200
WINSTON SALEM, NC 27105
Practice locations map

Location

Practice Location

2295 E 14TH ST STE 200, WINSTON SALEM, NC
(336) 716-3182

Quick Facts

NPI
1477203834
Entity Type
Individual
Gender
Female
Medicare
Not confirmed
Specialties
2
Locations
1
Publications
17

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