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ELIZABETH PETTY, MD
MD
Internal Medicine Physician
NPI: 1477661361IndividualAccepts Medicare
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
MD24627(TN)
CMS Specialties
PrimaryINTERNAL MEDICINE
Education
UNIVERSITY OF TENNESSEE, HSC, COLLEGE OF MEDICINE
Class of 1990
Research & Publications (20)
Duplication within the SEPT9 gene associated with a founder effect in North American families with hereditary neuralgic amyotrophy.
PMID 19139049·Hum Mol Genet·2009
8-other
Three distinct condensin complexes control C. elegans chromosome dynamics.
PMID 19119011·Curr Biol·2009
4-observational
Up-regulation of SEPT9_v1 stabilizes c-Jun-N-terminal kinase and contributes to its pro-proliferative activity in mammary epithelial cells.
PMID 19071215·Cell Signal·2009
8-other
CHFR: A Novel Mitotic Checkpoint Protein and Regulator of Tumorigenesis.
PMID 18633460·Transl Oncol·2008
8-other
Loss of CHFR in human mammary epithelial cells causes genomic instability by disrupting the mitotic spindle assembly checkpoint.
PMID 18592005·Neoplasia·2008
8-other
The role of steroid hormones in the NF1 phenotype: focus on pregnancy.
PMID 18481270·Am J Med Genet A·2008
6-review
Large P body-like RNPs form in C. elegans oocytes in response to arrested ovulation, heat shock, osmotic stress, and anoxia and are regulated by the major sperm protein pathway.
PMID 18439994·Dev Biol·2008
7-preclinical
Airway obstruction caused by PTEN hamartoma (Bannayan-Riley-Ruvalcaba) syndrome.
PMID 18025323·Arch Otolaryngol Head Neck Surg·2007
5-case
Characterization of a SEPT9 interacting protein, SEPT14, a novel testis-specific septin.
PMID 17922164·Mamm Genome·2007
7-preclinical
High SEPT9_v1 expression in human breast cancer cells is associated with oncogenic phenotypes.
PMID 17875694·Cancer Res·2007
8-other
Altered expression of the early mitotic checkpoint protein, CHFR, in breast cancers: implications for tumor suppression.
PMID 17596595·Cancer Res·2007
8-other
Beliefs about the etiology of homosexuality and about the ramifications of discovering its possible genetic origin.
PMID 17594974·J Homosex·2007
8-other
Applications and implications of advances in human genetics: perspectives from a group of Black Americans.
PMID 17380057·Community Genet·2007
8-other
Malignant triton tumor in a patient with Li-Fraumeni syndrome and a novel TP53 mutation.
PMID 16333835·Pediatr Blood Cancer·2007
5-case
Cloning and expression analysis of pos-1 in the nematodes Caenorhabditis briggsae and Caenorhabditis remanei.
PMID 15880508·Dev Dyn·2005
7-preclinical
Skewed X-inactivation in carriers establishes linkage in an X-linked deafness-mental retardation syndrome.
PMID 15389700·Am J Med Genet A·2004
8-other
Mutations in the slow skeletal muscle fiber myosin heavy chain gene (MYH7) cause laing early-onset distal myopathy (MPD1).
PMID 15322983·Am J Hum Genet·2004
4-observational
CHFR-associated early G2/M checkpoint defects in breast cancer cells.
PMID 14694445·Mol Carcinog·2004
8-other
The second kindred with autosomal dominant distal myopathy linked to chromosome 14q: genetic and clinical analysis.
PMID 12975303·Arch Neurol·2003
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 100 LANTANA RD, SUITE 202
CROSSVILLE, TN 38555 - Phone
- (931) 484-5141
Quick Facts
- NPI
- 1477661361
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 36
- Publications
- 20
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