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STEVEN WINOKUR, MD
MD
Internal Medicine Physician
NPI: 1821058280Individual
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
4301042416(MI)
Research & Publications (16)
Patient safety: mindful, meaningful, and fulfilling.
PMID 16223102·Front Health Serv Manage·2005
8-other
Expression profiling of FSHD muscle supports a defect in specific stages of myogenic differentiation.
PMID 14519683·Hum Mol Genet·2003
4-observational
Facioscapulohumeral muscular dystrophy (FSHD) myoblasts demonstrate increased susceptibility to oxidative stress.
PMID 12868502·Neuromuscul Disord·2003
4-observational
Specific loss of histone H3 lysine 9 trimethylation and HP1gamma/cohesin binding at D4Z4 repeats is associated with facioscapulohumeral dystrophy (FSHD).
PMID 19593370·PLoS Genet·2009
7-preclinical
RNA transcripts, miRNA-sized fragments and proteins produced from D4Z4 units: new candidates for the pathophysiology of facioscapulohumeral dystrophy.
PMID 19359275·Hum Mol Genet·2009
7-preclinical
DUX4, a candidate gene of facioscapulohumeral muscular dystrophy, encodes a transcriptional activator of PITX1.
PMID 17984056·Proc Natl Acad Sci U S A·2007
8-other
Gene selection for multiclass prediction by weighted Fisher criterion.
PMID 17713593·EURASIP J Bioinform Syst Biol·2007
8-other
RNAPol-ChIP analysis of transcription from FSHD-linked tandem repeats and satellite DNA.
PMID 17239456·Biochim Biophys Acta·2007
7-preclinical
Nuclear envelope dystrophies show a transcriptional fingerprint suggesting disruption of Rb-MyoD pathways in muscle regeneration.
PMID 16478798·Brain·2006
8-other
Variable hypomethylation of D4Z4 in facioscapulohumeral muscular dystrophy.
PMID 16178028·Ann Neurol·2005
4-observational
Localization of 4q35.2 to the nuclear periphery: is FSHD a nuclear envelope disease?
PMID 15238509·Hum Mol Genet·2004
4-observational
Hypomethylation of D4Z4 in 4q-linked and non-4q-linked facioscapulohumeral muscular dystrophy.
PMID 14634647·Nat Genet·2003
8-other
Methylation of the FSHD syndrome-linked subtelomeric repeat in normal and FSHD cell cultures and tissues.
PMID 11708861·Mol Genet Metab·2001
8-other
Oligonucleotide microarray expression analysis of genes whose expression is correlated with tumorigenic and non-tumorigenic phenotype of HeLa x human fibroblast hybrid cells.
PMID 11275370·Cancer Lett·2001
8-other
Characterization of the murine homolog of C1qR(P): identical cellular expression pattern, chromosomal location and functional activity of the human and murine C1qR(P).
PMID 11074255·Mol Immunol·2000
7-preclinical
The distribution of somatic H1 subtypes is non-random on active vs. inactive chromatin: distribution in human fetal fibroblasts.
PMID 10997781·Chromosome Res·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
- 630 CHERRY TREE LN
ROCHESTER HILLS, MI 48306 - Phone
- (248) 672-1275
Quick Facts
- NPI
- 1821058280
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 16
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