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SARAH MARTINELLI, DMD
DMD
Endodontics
NPI: 1457792343Individual
Specialties, Licenses & Credentials
EndodonticsPrimary
Dentist — Endodontics
Code: 1223E0200X
0442000183(VA)
Research & Publications (20)
RAS signaling dysregulation in human embryonal Rhabdomyosarcoma.
PMID 19681119·Genes Chromosomes Cancer·2009
8-other
Hematological indices at birth in relation to arterial and venous Doppler in small-for-gestational-age fetuses.
PMID 19551526·Acta Obstet Gynecol Scand·2009
8-other
Intraoperative transesophageal echocardiography diagnosis of residual tumor fragment after surgical removal of renal cell carcinoma.
PMID 18499590·Anesth Analg·2008
5-case
Increased expression of angiopoietin-2 characterizes early B-cell chronic lymphocytic leukemia with poor prognosis.
PMID 17928052·Leuk Res·2008
8-other
Genetic structure and molecular variability of Spodoptera frugiperda (Lepidoptera: Noctuidae) collected in maize and cotton fields in Brazil.
PMID 17524154·Bull Entomol Res·2007
7-preclinical
Targeting survivin via PI3K but not c-akt/PKB by anticancer drugs in immature neutrophils.
PMID 16715127·Oncogene·2006
7-preclinical
Induction of genes mediating interferon-dependent extracellular trap formation during neutrophil differentiation.
PMID 15302890·J Biol Chem·2004
8-other
Increased angiogenesis induced by chronic lymphocytic leukemia B cells is mediated by leukemia-derived Ang2 and VEGF.
PMID 19616847·Leuk Res·2010
8-other
Congenital heart block not associated with anti-Ro/La antibodies: comparison with anti-Ro/La-positive cases.
PMID 19567621·J Rheumatol·2009
4-observational
Interferon-alpha may restore sensitivity to tyrosine-kinase inhibitors in Philadelphia chromosome positive acute lymphoblastic leukaemia with F317L mutation.
PMID 19545285·Br J Haematol·2009
5-case
Biomarkers of oxidative stress in babies at high risk for retinopathy of prematurity.
PMID 19482670·Front Biosci (Elite Ed)·2009
3-trial
Spectrum of MEK1 and MEK2 gene mutations in cardio-facio-cutaneous syndrome and genotype-phenotype correlations.
PMID 19156172·Eur J Hum Genet·2009
8-other
Development of hypogammaglobulinemia in patients treated with imatinib for chronic myeloid leukemia or gastrointestinal stromal tumor.
PMID 18519520·Haematologica·2008
8-other
Diverse driving forces underlie the invariant occurrence of the T42A, E139D, I282V and T468M SHP2 amino acid substitutions causing Noonan and LEOPARD syndromes.
PMID 18372317·Hum Mol Genet·2008
8-other
Somatically acquired JAK1 mutations in adult acute lymphoblastic leukemia.
PMID 18362173·J Exp Med·2008
7-preclinical
Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy.
PMID 17603483·Nat Genet·2007
7-preclinical
Predicting preterm delivery in asymptomatic patients with prior preterm delivery by measurement of cervical length and phosphorylated insulin-like growth factor-binding protein-1.
PMID 17444550·Ultrasound Obstet Gynecol·2007
8-other
Angiopoietin-2 expression in B-cell chronic lymphocytic leukemia: association with clinical outcome and immunoglobulin heavy-chain mutational status.
PMID 17361220·Leukemia·2007
8-other
Structural and functional effects of disease-causing amino acid substitutions affecting residues Ala72 and Glu76 of the protein tyrosine phosphatase SHP-2.
PMID 17177198·Proteins·2007
8-other
Gain-of-function SOS1 mutations cause a distinctive form of Noonan syndrome.
PMID 17143282·Nat Genet·2007
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
- 2 HOLMES RD
LENOX, MA 01240 - Phone
- (703) 801-8003
Quick Facts
- NPI
- 1457792343
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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