Suchergebnisse - "Asgaritarghi, Golareh"

PubPharm (7)

1

Anti-Cancer Role of Dendrosomal Nano Solanine in Chronic Myelogenous Leukemia Cell Line through Attenuation of PI3K/AKT/mTOR Signaling Pathway and Inhibition of hTERT Expression

enthalten in: Current molecular pharmacology | 2023

von Asgaritarghi, G. | Farsani, S. | Sadeghizadeh, D. | +2

2

M13 phage coated surface elicits an anti-inflammatory response in BALB/c and C57BL/6 peritoneal macrophages

enthalten in: International immunopharmacology | 2022

von Safari, Z. | Sadeghizadeh, M. | Asgaritarghi, G. | +3

3

Novel manifestations of Warburg micro syndrome type 1 caused by a new splicing variant of RAB3GAP1 : a case report

enthalten in: BMC neurology | 2021

von Khalesi, R. | Razmara, E. | Asgaritarghi, G. | +4

4

Novel manifestations of Warburg micro syndrome type 1 caused by a new splicing variant of RAB3GAP1: a case report

enthalten in: BMC neurology | 2021

von Khalesi, R. | Razmara, E. | Asgaritarghi, G. | +4

5

Combination treatment of dendrosomal nanocurcumin and low-level laser therapy develops proliferation and migration of mouse embryonic fibroblasts and alter TGF-β, VEGF, TNF-α and IL-6 expressions involved in wound healing process

enthalten in: PloS one | 2021

von Ebrahiminaseri, A. | Sadeghizadeh, M. | Moshaii, A. | +2

6

Novel homozygous variants in the TMC1 and CDH23 genes cause autosomal recessive nonsyndromic hearing loss

enthalten in: Molecular genetics & genomic medicine | 2020

von Zardadi, S. | Razmara, E. | Asgaritarghi, G. | +6

7

Novel homozygous variants in the TMC1 and CDH23 genes cause autosomal recessive nonsyndromic hearing loss

enthalten in: Molecular Genetics & Genomic Medicine | 2020

von Zardadi, S. | Razmara, E. | Asgaritarghi, G. | +6

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