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RANDY SHEMER, D.O.
D.O.
Internal Medicine Physician
NPI: 1376567610IndividualAccepts Medicare
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
OS-008808L(PA)
Education
WEST VIRGINIA SCHOOL OF OSTEOPATHIC MEDICINE
Class of 1995
Research & Publications (20)
Regulation of the transcription factor Gcn4 by Pho85 cyclin PCL5.
PMID 12101234·Mol Cell Biol·2002
8-other
A highly polymorphic degenerate microsatellite for molecular strain typing of Candida krusei.
PMID 11495980·Microbiology (Reading)·2001
8-other
The imprinting box of the Prader-Willi/Angelman syndrome domain.
PMID 11101841·Nat Genet·2000
7-preclinical
Protein-binding elements establish in the oocyte the primary imprint of the Prader-Willi/Angelman syndromes domain.
PMID 19506242·Proc Natl Acad Sci U S A·2009
7-preclinical
MeCP2 involvement in the regulation of neuronal alpha-tubulin production.
PMID 19174478·Hum Mol Genet·2009
7-preclinical
An endocytic mechanism for haemoglobin-iron acquisition in Candida albicans.
PMID 18466294·Mol Microbiol·2008
4-observational
SERKAL syndrome: an autosomal-recessive disorder caused by a loss-of-function mutation in WNT4.
PMID 18179883·Am J Hum Genet·2008
8-other
KRT14 haploinsufficiency results in increased susceptibility of keratinocytes to TNF-alpha-induced apoptosis and causes Naegeli-Franceschetti-Jadassohn syndrome.
PMID 18049449·J Invest Dermatol·2008
8-other
The Prader-Willi/Angelman imprinted domain and its control center.
PMID 16575193·Cytogenet Genome Res·2006
7-preclinical
Splicing mutation associated with Rett syndrome and an experimental approach for genetic diagnosis.
PMID 16133181·Hum Genet·2005
8-other
MeCP2 deficiency in Rett syndrome causes epigenetic aberrations at the PWS/AS imprinting center that affects UBE3A expression.
PMID 15757975·Hum Mol Genet·2005
7-preclinical
Establishing the epigenetic status of the Prader-Willi/Angelman imprinting center in the gametes and embryo.
PMID 15367489·Hum Mol Genet·2004
7-preclinical
Ubiquitylation of synphilin-1 and alpha-synuclein by SIAH and its presence in cellular inclusions and Lewy bodies imply a role in Parkinson's disease.
PMID 15064394·Proc Natl Acad Sci U S A·2004
7-preclinical
Control elements within the PWS/AS imprinting box and their function in the imprinting process.
PMID 14962980·Hum Mol Genet·2004
7-preclinical
Expression and localization of components of the histone deacetylases multiprotein repressory complexes in the mouse preimplantation embryo.
PMID 14643676·Gene Expr Patterns·2003
7-preclinical
The imprinting mechanism of the Prader-Willi/Angelman regional control center.
PMID 12411498·EMBO J·2002
8-other
Deletion of the copper transporter CaCCC2 reveals two distinct pathways for iron acquisition in Candida albicans.
PMID 12067343·Mol Microbiol·2002
7-preclinical
The mouse Snrpn minimal promoter and its human orthologue: activity and imprinting.
PMID 11733034·Genes Cells·2001
7-preclinical
Isolation and characterization of medaka ribosomal protein S3a (fte-1) cDNA and gene.
PMID 10854794·Gene·2000
4-observational
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 2424 MILL ST
ALIQUIPPA, PA 15001 - Phone
- (724) 770-0771
Quick Facts
- NPI
- 1376567610
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 31
- Publications
- 20
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