David N Finegold
Overview
Explore the profile of David N Finegold including associated specialties, affiliations and a list of published articles.
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45
Citations
1192
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Recent Articles
11.
Eshbach M, Sethi R, Avula R, Lamb J, Hollingshead D, Finegold D, et al.
Am J Physiol Renal Physiol
. 2017 Jun;
313(3):F585-F595.
PMID: 28615248
The OK cell line derived from the kidney of a female opossum has proven to be a useful model in which to investigate the unique regulation of ion transport and...
12.
Pan L, Martin P, Zimmer T, Segreti A, Kassiff S, McKain B, et al.
Am J Psychiatry
. 2016 Aug;
174(1):42-50.
PMID: 27523499
Objective: Treatment-refractory depression is a devastating condition with significant morbidity, mortality, and societal cost. At least 15% of cases of major depressive disorder remain refractory to treatment. The authors previously...
13.
Weinreb N, Finegold D, Feingold E, Zeng Z, Rosenbloom B, Shankar S, et al.
Orphanet J Rare Dis
. 2015 May;
10:64.
PMID: 25994334
Background: GD1-DS3 is an integrated assessment of type 1 Gaucher disease (GD1) burden based on bone, hematologic and visceral domains. We investigated this disease severity scoring system (DS3) methodology for...
14.
Soran A, Finegold D, Brufsky A
Oncology (Williston Park)
. 2012 May;
26(3):249, 254, 256.
PMID: 22545306
No abstract available.
15.
Finegold D, Baty C, Knickelbein K, Perschke S, Noon S, Campbell D, et al.
Clin Cancer Res
. 2012 Feb;
18(8):2382-90.
PMID: 22351697
Purpose: Secondary lymphedema is a frequent complication of breast cancer associated with surgery, chemotherapy, or radiation following breast cancer treatment. The potential contribution of genetic susceptibility to risk of developing...
16.
Ruffner M, Finegold D, MacGinnitie A
Acta Paediatr
. 2011 Sep;
100(10):1289, 1394-5.
PMID: 21916981
No abstract available.
17.
Yusupov R, Finegold D, Naylor E, Sahai I, Waisbren S, Levy H
Mol Genet Metab
. 2010 Jun;
101(1):33-9.
PMID: 20580581
Introduction: Medium chain acyl-CoA dehydrogenase deficiency (MCADD) is the most frequent of the fatty acid oxidation disorders (FAOD), a group caused by defects in the mitochondrial B-oxidation of fatty acids....
18.
Ferrell R, Baty C, Kimak M, Karlsson J, Lawrence E, Franke-Snyder M, et al.
Am J Hum Genet
. 2010 Jun;
86(6):943-8.
PMID: 20537300
Lymphedema is the clinical manifestation of defects in lymphatic structure or function. Mutations identified in genes regulating lymphatic development result in inherited lymphedema. No mutations have yet been identified in...
19.
Cray Jr J, Burrows A, Vecchione L, Lensie E, DeCesare G, Campbell A, et al.
J Craniofac Surg
. 2010 May;
21(3):711-8.
PMID: 20485034
Research has implicated the faulty regulation of transforming growth factor beta signaling as one mechanism for premature calvaria suture fusion. Androgens have been shown to increase the expression and activity...
20.
Conley Y, Mukherjee A, Kammerer C, DeKosky S, Kamboh M, Finegold D, et al.
Am J Med Genet B Neuropsychiatr Genet
. 2008 Nov;
150B(5):703-9.
PMID: 19035514
The calcium-sensing receptor (CASR) is a G-protein coupled, transmembrane receptor that responds to changes in Ca(2+) levels. We hypothesized that the CASR could have a role in Alzheimer disease (AD)...