Search Results - "Eker, Candan"

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  1. 1

    JAK2V617F Mutation in Endothelial Cells of Patients with Atherosclerotic Carotid Disease by Diz-Küçükkaya, Reyhan, İyigün, Taner, Albayrak, Özgür, Eker, Candan, Günel, Tuba

    Published in Turkish journal of haematology (01-09-2024)
    “…It has been shown that clonal mutations occur in hematopoietic stem cells with advancing age and increase the risk of death due to atherosclerotic vascular…”
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    Journal Article
  2. 2

    Investigation of human paternal mitochondrial DNA transmission in ART babies whose fathers with male infertility by Eker, Candan, Celik, Hale Goksever, Balci, Burcin Karamustafaoglu, Gunel, Tuba

    “…To investigate the paternal mitochondrial DNA’s effect on assisted reproductive technology (ART) applications and possible paternal mitochondrial DNA…”
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    Journal Article
  3. 3
  4. 4

    JAK2 V617F Mutation in Endothelial Cells of Patients with Atherosclerotic Carotid Disease by Diz-Küçükkaya, Reyhan, İyigün, Taner, Albayrak, Özgür, Eker, Candan, Günel, Tuba

    Published in Turkish journal of haematology (28-08-2024)
    “…It has been shown that clonal mutations occur in hematopoietic stem cells with advancing age and increase the risk of death due to atherosclerotic vascular…”
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    Journal Article
  5. 5

    The significance of MUM1/IRF4 protein expression and IRF4 translocation of CD30(+) cutaneous T-cell lymphoproliferative disorders: A study of 53 cases by Kiran, Tugce, Demirkesen, Cuyan, Eker, Candan, Kumusoglu, Hakki, Tuzuner, Nukhet

    Published in Leukemia research (01-04-2013)
    “…Abstract Current laboratory technics, clinicopathologic findings cannot always reliably distinguish primary cutaneous CD30(+) lymphoproliferative disorders…”
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    Journal Article
  6. 6

    The genomic analysis of endometrial mitochondrial DNA copy number variation on recurrent implantation failure by Eker, Candan, Basdas, Rumeysa, Balci, Burcin Karamustafaoglu, Bastu, Ercan, Gunel, Tuba

    “…Aim of this study was to define the relationship between RIF (Recurrent Implantation Failure) and endometrial mtDNA copy number. A total of 50 women of…”
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    Journal Article
  7. 7

    The Role of rs4626 and rs7221352 Polymorphisms on the TOB1 Gene in Turkish Relapsing-Remitting Multiple Sclerosis Patients by Koseahmet, Fulya Basoglu, Eker, Candan, Ozturk, Musa, Ozdemir, Sebnem, Koksal, Ayhan, Baybas, Sevim, Gunel, Tuba

    Published in European journal of biology (01-12-2022)
    “…Objective: Multiple sclerosis often causes neurological disability and reduced quality of life. Genetic biomarkers are important tools for the diagnosis and…”
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    Journal Article