Search Results - "Eskandari, Nasim"

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  1. 1

    Cryopreservation of human umbilical vein and porcine corneal endothelial cell monolayers by Eskandari, Nasim, Marquez-Curtis, Leah A., McGann, Locksley E., Elliott, Janet A.W.

    Published in Cryobiology (01-12-2018)
    “…Cryopreservation of endothelium is one of the major challenges in the cryopreservation of complex tissues. Human umbilical vein endothelial cells (HUVECs) in…”
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    Journal Article
  2. 2

    Spinal neurovascular coupling is preserved despite time-dependent alterations of spinal cord blood flow responses in a rat model of chronic back pain: implications for functional spinal cord imaging by Paquette, Thierry, Eskandari, Nasim, Leblond, Hugues, Piché, Mathieu

    Published in Pain (Amsterdam) (01-04-2023)
    “…Functional magnetic resonance imaging has been used to investigate nociceptive processes in patients with chronic pain. However, the results may be confounded…”
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    Journal Article
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    Protocol for Cryopreservation of Endothelial Monolayers by Marquez-Curtis, Leah A, Eskandari, Nasim, McGann, Locksley E, Elliott, Janet A W

    “…One of the major challenges in the preservation of complex tissues is the cryosensitivity of the endothelium, the single layer of cells lining blood vessels,…”
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    Thermal expansion of substrate may affect adhesion of Chinese hamster fibroblasts to surfaces during freezing by Rutt, Taylor, Eskandari, Nasim, Zhurova, Maria, Elliott, Janet A.W., McGann, Locksley E., Acker, Jason P., Nychka, John A.

    Published in Cryobiology (01-02-2019)
    “…Despite success in cryopreservation of cells in suspension, cryopreservation of cells in monolayers is still challenging. One of the major problems is…”
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    Journal Article
  8. 8

    Study of Sperm Chromatin in Infertile Men with Globozoospermia: A Systematic Review Article by Marziyeh Tavalaee, Nasim Eskandari, Mohammad Hossein Nasr-Esfahani

    “…Background and Aim: Globozoospermia is a severe sperm morphological abnormality in men that characterized by round-headed spermatozoa with low or absence…”
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  9. 9

    Three novel mutations in Iranian patients with Tay-Sachs disease by Jamali, Solmaz, Eskandari, Nasim, Aryani, Omid, Salehpour, Shadab, Zaman, Talieh, Kamalidehghan, Behnam, Houshmand, Massoud

    Published in Iranian biomedical journal (2014)
    “…Tay-Sachs disease (TSD), or GM2 gangliosidosis, is a lethal autosomal recessive neurodegenerative disorder, which is caused by a deficiency of…”
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    Journal Article