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ELIZABETH GINELLI, MD
MD
Student in an Organized Health Care Education/Training Program
NPI: 1841812849Individual
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training ProgramPrimary
Student in an Organized Health Care Education/Training Program
Code: 390200000X
4351053786(MI)
Research & Publications (17)
Remodeling of the chromatin structure of the facioscapulohumeral muscular dystrophy (FSHD) locus and upregulation of FSHD-related gene 1 (FRG1) expression during human myogenic differentiation.
PMID 19607661·BMC Biol·2009
8-other
Evolutionary genomic remodelling of the human 4q subtelomere (4q35.2).
PMID 17359533·BMC Evol Biol·2007
7-preclinical
Forced expression of RDH10 gene retards growth of HepG2 cells.
PMID 17218779·Cancer Biol Ther·2007
8-other
The boundary of macaque rDNA is constituted by low-copy sequences conserved during evolution.
PMID 16765020·Genomics·2006
4-observational
Influence of intermediate and uninterrupted FMR1 CGG expansions in premature ovarian failure manifestation.
PMID 16361284·Hum Reprod·2006
8-other
Mutation analysis of two candidate genes for premature ovarian failure, DACH2 and POF1B.
PMID 15459172·Hum Reprod·2004
8-other
Evolution of beta satellite DNA sequences: evidence for duplication-mediated repeat amplification and spreading.
PMID 15201396·Mol Biol Evol·2004
7-preclinical
Mutations in the coding region of the FOXL2 gene are not a major cause of idiopathic premature ovarian failure.
PMID 15181179·Mol Hum Reprod·2004
8-other
Genomic organization and transcription of the human retinol dehydrogenase 10 (RDH10) gene.
PMID 14596915·FEBS Lett·2003
8-other
Gene expression analysis in interstitial lung edema induced by saline infusion.
PMID 12853120·Biochim Biophys Acta·2003
7-preclinical
Human genome dispersal and evolution of 4q35 duplications and interspersed LSau repeats.
PMID 12383499·Gene·2002
7-preclinical
Mutation analysis of the inhibin alpha gene in a cohort of Italian women affected by ovarian failure.
PMID 12093833·Hum Reprod·2002
8-other
The structure of duplications on human acrocentric chromosome short arms derived by the analysis of 15p.
PMID 11499671·Hum Genet·2001
8-other
Molecular definition of Xq common-deleted region in patients affected by premature ovarian failure.
PMID 11129329·Hum Genet·2000
8-other
Molecular structure and evolution of DNA sequences located at the alpha satellite boundary of chromosome 20.
PMID 11054534·Gene·2000
7-preclinical
Iron overload and gene expression in HepG2 cells: analysis by differential display.
PMID 10713272·FEBS Lett·2000
8-other
Association between idiopathic premature ovarian failure and fragile X premutation.
PMID 10611212·Hum Reprod·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
- 1500 E MEDICAL CENTER DR, SPC 5033, TAUBMAN CENTER, FLOOR 2, RECEPTION C
ANN ARBOR, MI 48109 - Phone
- (734) 936-5738
Quick Facts
- NPI
- 1841812849
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 17
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