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KEREN SPERLING, D.M.D, M.S.C
D.M.D, M.S.C
Periodontics
NPI: 1588898266Individual
Specialties, Licenses & Credentials
PeriodonticsPrimary
Dentist — Periodontics
Code: 1223P0300X
0401412356(VA)
Research & Publications (20)
The orthopoxvirus 68-kilodalton ankyrin-like protein is essential for DNA replication and complete gene expression of modified vaccinia virus Ankara in nonpermissive human and murine cells.
PMID 19357172·J Virol·2009
7-preclinical
Novel EXT1 and EXT2 mutations in hereditary multiple exostoses families of Indian origin.
PMID 19309273·Genet Test Mol Biomarkers·2009
8-other
Novel mutation in the gamma-S crystallin gene causing autosomal dominant cataract.
PMID 19262743·Mol Vis·2009
5-case
A systematic proteomic study of irradiated DNA repair deficient Nbn-mice.
PMID 19412544·PLoS One·2009
7-preclinical
A mutation in GJA8 (p.P88Q) is associated with "balloon-like" cataract with Y-sutural opacities in a family of Indian origin.
PMID 18587493·Mol Vis·2008
8-other
Age and origin of major Smith-Lemli-Opitz syndrome (SLOS) mutations in European populations.
PMID 17965227·J Med Genet·2008
7-preclinical
High-affinity binding of southern African HIV type 1 subtype C envelope protein, gp120, to the CCR5 coreceptor.
PMID 19018669·AIDS Res Hum Retroviruses·2008
8-other
A novel mutation in GJA8 associated with jellyfish-like cataract in a family of Indian origin.
PMID 18334946·Mol Vis·2008
8-other
The highly conserved orthopoxvirus 68k ankyrin-like protein is part of a cellular SCF ubiquitin ligase complex.
PMID 18353424·Virology·2008
7-preclinical
Extreme variation in apoptosis capacity amongst lymphoid cells of Nijmegen breakage syndrome patients.
PMID 17977616·Eur J Cell Biol·2008
8-other
A novel mutation in the connexin 46 (GJA3) gene associated with autosomal dominant congenital cataract in an Indian family.
PMID 17893674·Mol Vis·2007
8-other
Nijmegen breakage syndrome (NBS) due to maternal isodisomy of chromosome 8.
PMID 17103455·Am J Med Genet A·2007
5-case
Polymorphisms in the DNA ligase IV gene might influence the risk of acute lymphoblastic leukemia in children.
PMID 17541392·Leukemia·2007
8-other
Cancer risk of heterozygotes with the NBN founder mutation.
PMID 18073374·J Natl Cancer Inst·2007
8-other
Molecular genetic analysis of NBS1 in German melanoma patients.
PMID 17496786·Melanoma Res·2007
8-other
A recurrent FBN1 mutation in an autosomal dominant ectopia lentis family of Indian origin.
PMID 18079676·Mol Vis·2007
8-other
The granulocyte nucleus and lamin B receptor: avoiding the ovoid.
PMID 17245605·Chromosoma·2007
6-review
Cancer incidence in Nijmegen breakage syndrome is modulated by the amount of a variant NBS protein.
PMID 16840438·Carcinogenesis·2007
8-other
A novel mutation in GJA8 associated with autosomal dominant congenital cataract in a family of Indian origin.
PMID 17110920·Mol Vis·2006
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
- 303 MAPLE AVE W STE H
VIENNA, VA 22180 - Phone
- (571) 234-1344
Quick Facts
- NPI
- 1588898266
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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