Golara Nasiri
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Golara Nasiri has a total of 11 co-authors. Here are the top co-authors by number of shared publications:
- Ali Rayat Pisheh
Department of Biology, Payam Noor University (PUN), Shiraz, Iran
2 shared publications - Hossein Rayat Pisheh
Department of Tissue Engineering and Applied Cell Sciences, School of Advanced Medical Sciences and Technologies, Shiraz University of Medical Sciences, Shiraz, Iran
2 shared publications Ali Kashi
Department of Chemistry, Amirkabir University of Technology (Tehran Polytechnic), Tehran, Iran
1 shared publication- Aliakbar Alizadeh
Department of Tissue Engineering and Applied Cell Sciences, School of Advanced Medical Sciences and Technologies, Shiraz University of Medical Sciences, Shiraz, Iran
1 shared publication - Farnaz Sani
Shiraz Institute for Stem Cell & Regenerative Medicine, Shiraz University of Medical Sciences, Shiraz, Iran
1 shared publication - Lobat Tayebi
Institute for Engineering in Medicine, Health, & Human Performance (EnMed), Batten College of Engineering and Technology, Old Dominion University, Norfolk, VA 23529, USA
1 shared publication
Latest Publications
- Open Access
- 10 September 2026
- Published by Springer Nature in Journal of Biological Engineering
Oxygen-releasing wound dressings: from molecular mechanisms to smart therapeutic platforms
- 10 September 2026
- Published by Springer Nature in Journal of Biological Engineering
Open AccessOxygen-releasing wound dressings: from molecular mechanisms to smart therapeutic platforms
- Open Access
- 10 August 2026
- Published by Springer Nature in Stem Cell Research & Therapy
- Vol. 17 (1)
Milk-derived exosomes (MDEs) as emerging nanotherapeutics in regenerative medicine
Milk-derived exosomes (MDEs) are naturally occurring nanoscale extracellular vesicles with unique biocompatibility, stability, and intrinsic capacity to ca
- 10 August 2026
- Published by Springer Nature in Stem Cell Research & Therapy
- Vol. 17 (1)
Open AccessMilk-derived exosomes (MDEs) as emerging nanotherapeutics in regenerative medicine
Milk-derived exosomes (MDEs) are naturally occurring nanoscale extracellular vesicles with unique biocompatibility, stability, and intrinsic capacity to ca
- Open Access
- 29 September 2020
- Published by Springer Nature in Stem Cell Research & Therapy
- Vol. 11 (1) , 1-11
Shedding light on the role of keratinocyte-derived extracellular vesicles on skin-homing cells
Extracellular vesicles (EVs) are secretory lipid membranes with the ability to regulate cellular functions by exchanging biological components between different cells. Resident skin cells such as keratinocytes, fibroblasts, melanocytes, and inflammatory cells can secrete different types of EVs depending on their biological state. These vesicles can influence the physiological properties and pathological processes of skin, such as pigmentation, cutaneous immunity, and wound healing. Since keratinocytes constitute the majority of skin cells, secreted EVs from these cells may alter the pathophysiological behavior of other skin cells. This paper reviews the contents of keratinocyte-derived EVs and their impact on fibroblasts, melanocytes, and immune cells to provide an insight for better understanding of the pathophysiological mechanisms of skin disorders and their use in related therapeutic approaches.
- 29 September 2020
- Published by Springer Nature in Stem Cell Research & Therapy
- Vol. 11 (1) , 1-11
Open AccessShedding light on the role of keratinocyte-derived extracellular vesicles on skin-homing cells
Extracellular vesicles (EVs) are secretory lipid membranes with the ability to regulate cellular functions by exchanging biological components between different cells. Resident skin cells such as keratinocytes, fibroblasts, melanocytes, and inflammatory cells can secrete different types of EVs depending on their biological state. These vesicles can influence the physiological properties and pathological processes of skin, such as pigmentation, cutaneous immunity, and wound healing. Since keratinocytes constitute the majority of skin cells, secreted EVs from these cells may alter the pathophysiological behavior of other skin cells. This paper reviews the contents of keratinocyte-derived EVs and their impact on fibroblasts, melanocytes, and immune cells to provide an insight for better understanding of the pathophysiological mechanisms of skin disorders and their use in related therapeutic approaches.