Dana Fuchs-Telem
Overview
Explore the profile of Dana Fuchs-Telem including associated specialties, affiliations and a list of published articles.
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Articles
15
Citations
315
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0
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Recent Articles
1.
Samuelov L, Bochner R, Magal L, Malovitski K, Sagiv N, Nousbeck J, et al.
Exp Dermatol
. 2021 Nov;
31(4):567-576.
PMID: 34787924
Background: Psoriasis is characterized by aberrant activation of several pro-inflammatory circuits as well as abnormal hyperproliferation and dysregulated apoptosis of keratinocytes (KCs). Most currently available therapeutic options primarily target psoriasis-associated...
2.
Allen H, Shraga-Heled N, Blumenfeld M, Dego-Ashto T, Fuchs-Telem D, Gilert A, et al.
Sci Rep
. 2018 Jan;
8(1):670.
PMID: 29330447
Culturing 3D-expanded human placental-derived adherent stromal cells (ASCs) in the presence of tumor necrosis factor-alpha (TNF-α) and interferon-gamma (IFN-γ) transiently upregulated the secretion of numerous anti-proliferative, anti-angiogenic and pro-inflammatory cytokines....
3.
Zahavi-Goldstein E, Blumenfeld M, Fuchs-Telem D, Pinzur L, Rubin S, Aberman Z, et al.
Cytotherapy
. 2017 Nov;
19(12):1438-1446.
PMID: 29122516
Background: In peripheral artery disease (PAD), blockage of the blood supply to the limbs, most frequently the legs, leads to impaired blood flow and tissue ischemia. Pluristem's PLX-PAD cells are...
4.
Warshauer E, Samuelov L, Sarig O, Vodo D, Bindereif A, Kanaan M, et al.
Exp Dermatol
. 2015 May;
24(8):618-22.
PMID: 25939713
Alopecia-neurological defects-endocrinopathy (ANE) syndrome is a rare inherited hair disorder, which was shown to result from decreased expression of the RNA-binding motif protein 28 (RBM28). In this study, we attempted...
5.
Li Q, Chung H, Ross N, Keller M, Andrews J, Kingman J, et al.
J Invest Dermatol
. 2015 Mar;
135(7):1905-1908.
PMID: 25734815
No abstract available.
6.
Eytan O, Fuchs-Telem D, Mevorach B, Indelman M, Bergman R, Sarig O, et al.
J Invest Dermatol
. 2014 Jan;
134(6):1752-1754.
PMID: 24463422
No abstract available.
7.
Eytan O, Morice-Picard F, Sarig O, Ezzedine K, Isakov O, Li Q, et al.
Am J Hum Genet
. 2013 Oct;
93(4):752-7.
PMID: 24075184
The coexistence of abnormal keratinization and aberrant pigmentation in a number of cornification disorders has long suggested a mechanistic link between these two processes. Here, we deciphered the genetic basis...
8.
Sarig O, Goldsher D, Nousbeck J, Fuchs-Telem D, Cohen-Katsenelson K, Iancu T, et al.
Am J Med Genet A
. 2013 Aug;
161A(9):2204-15.
PMID: 23918762
3-Methylglutaconic aciduria (3-MGCA) type IV is defined as a heterogeneous group of inborn errors featuring in common 3-MGCA and associated with primary mitochondrial dysfunction leading to a spectrum of multisystem...
9.
Nousbeck J, Padalon-Brauch G, Fuchs-Telem D, Israeli S, Sarig O, Sheffer R, et al.
J Invest Dermatol
. 2013 Apr;
133(11):2626-2628.
PMID: 23604102
No abstract available.
10.
Goldsmith T, Fuchs-Telem D, Israeli S, Sarig O, Padalon-Brauch G, Bergman R, et al.
Exp Dermatol
. 2013 Mar;
22(4):251-4.
PMID: 23528209
Autosomal recessive congenital ichthyosis refers to a heterogeneous group of cornification disorders of major impact on patients' life. The disease has been linked so far to mutations in 8 distinct...