Ekim Z Taskiran
Overview
Explore the profile of Ekim Z Taskiran including associated specialties, affiliations and a list of published articles.
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40
Citations
401
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Recent Articles
1.
Tasdemir N, Kilicarslan B, Imren G, Karaosmanoglu B, Taskiran E, Bayram C
J R Soc Interface
. 2025 Feb;
22(223):20240642.
PMID: 39999880
The concept of preconditioning mesenchymal stem cells (MSCs) under different stress conditions or with bioactive molecules is introduced to optimize their therapeutic potential. This study investigates the physicochemical effect of...
2.
Imren G, Karaosmanoglu B, Muratoglu B, Ozdemir C, Utine G, Simsek-Kiper P, et al.
Int J Mol Sci
. 2025 Feb;
26(3).
PMID: 39940902
Skeletal dysplasias, characterized by bone, cartilage, and connective tissue abnormalities, often arise due to disruptions in extracellular matrix (ECM) dynamics and growth factor-dependent signaling pathways. RSPRY1, a secreted protein with...
3.
Ozisin M, Imren G, Aydin B, Karaosmanoglu B, Taskiran E
Mol Biol Rep
. 2025 Jan;
52(1):120.
PMID: 39804499
Background: La-related protein 7 (LARP7) is a key regulator of RNA metabolism and is thought to play a role in various cellular processes. LARP7 gene autosomal recessive mutations are the...
4.
Bayram C, Ozturk S, Karaosmanoglu B, Gultekinoglu M, Taskiran E, Ulubayram K, et al.
Macromol Biosci
. 2024 Oct;
24(12):e2400279.
PMID: 39388643
The combination of gelatin and hydroxyapatite (HA) has emerged as a promising strategy in dental tissue engineering due to its favorable biocompatibility, mechanical properties, and ability to support cellular activities...
5.
Karaosmanoglu B, Imren G, Ozisin M, Recber T, Simsek Kiper P, Haliloglu G, et al.
Mol Biol Rep
. 2024 Sep;
51(1):979.
PMID: 39269588
Background: Rett syndrome (RTT) is a rare neurodevelopmental disorder that primarily affects females and is characterized by a period of normal development followed by severe cognitive, motor, and communication impairment....
6.
Karaosmanoglu B, Imren G, Uner M, Orhan D, Gucer S, Turer O, et al.
Pathol Res Pract
. 2024 May;
258:155334.
PMID: 38718468
Placental transmogrification of the lung (PTL) is a rare pulmonary condition characterized by the presence of immature placental villous structures. The etiology and molecular mechanisms underlying this disease remain largely...
7.
Parveen M, Karaosmanoglu B, Sucularli C, Uner A, Taskiran E, Esendagli G
Eur J Immunol
. 2024 Mar;
54(5):e2350717.
PMID: 38462943
Resistance to immunity is associated with the selection of cancer cells with superior capacities to survive inflammatory reactions. Here, we tailored an ex vivo immune selection model for acute myeloid...
8.
Karaosmanoglu B, Imren G, Utine E, Sekeroglu H, Taskiran E
Exp Eye Res
. 2024 Feb;
241:109833.
PMID: 38369231
Retinal dystrophies are a common health problem worldwide that are currently incurable due to the inability of retinal cells to regenerate. Inherited retinal diseases (IRDs) are a diverse group of...
9.
Lafci N, Karaosmanoglu B, Taskiran E, Simsek-Kiper P, Utine G
Mol Syndromol
. 2023 Jun;
14(3):258-265.
PMID: 37323203
Introduction: Mowat-Wilson syndrome (MWS) is an autosomal-dominant complex developmental disorder characterized by distinctive facial appearance, intellectual disability, epilepsy, and various clinically heterogeneous abnormalities reminiscent of neurocristopathies. MWS is caused by...
10.
Akalin A, Simsek-Kiper P, Taskiran E, Karaosmanoglu B, Utine G, Boduroglu K
Am J Med Genet A
. 2023 Jan;
191(4):1119-1127.
PMID: 36630262
Primordial dwarfism (PD) is one of a highly heterogeneous group of disorders characterized by severe prenatal/postnatal growth restriction. Defects in various pathways such as DNA repair mechanism, impaired centrioles, abnormal...