Search Results - "Paridar, Mostafa"

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  1. 1

    Autophagy regulation and its role in normal and malignant hematopoiesis by Shahrabi, Saeid, Paridar, Mostafa, Zeinvand‐Lorestani, Marzieh, Jalili, Arsalan, Zibara, Kazem, Abdollahi, Mohammad, Khosravi, Abbas

    Published in Journal of cellular physiology (01-12-2019)
    “…Autophagy, the molecular machinery of self‐eating, plays a dual role of a tumor promoter and tumor suppressor. This mechanism affects different clinical…”
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    Journal Article
  2. 2

    Clinico-Hematological and cytogenetic spectrum of adult myelodysplastic syndrome: The first retrospective cross-sectional study in Iranian patients by Paridar, Mostafa, Zibara, Kazem, Ahmadi, Seyed Esmaeil, Khosravi, Abbas, Soleymani, Maral, Azizi, Ebrahim, Ghalesardi, Omid Kiani

    Published in Molecular cytogenetics (08-05-2021)
    “…Myelodysplastic syndrome (MDS), a heterogeneous group of hematopoietic malignancy, has been shown to present different cytogenetic abnormalities, risk factors,…”
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  3. 3

    Reference interval of antithrombin, protein C, and protein S activities in healthy adults in Iran, the effect of age, sex, oral contraceptive intake, and menopause by Tabibian, Shadi, Khoshmirsafa, Majid, Paridar, Mostafa, Motevalian, Abbas, Shekarabi, Mahdi, Safa, Majid

    “…Background Antithrombin (AT), protein C (PC), and protein S (PS) are natural anticoagulant proteins that deficiency in each of them is associated with an…”
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    Journal Article
  4. 4

    Iranian patients with hemoglobin H disease: genotype–phenotype correlation by Paridar, Mostafa, Azizi, Ebrahim, Keikhaei, Bijan, Takhviji, Vahideh, Baluchi, Iman, Khosravi, Abbas

    Published in Molecular biology reports (01-10-2019)
    “…Thalassemia is one of the most common monogenic hereditary disorders. Despite noticeable advances made in prevention strategies, it is still highly prevalent…”
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  5. 5
  6. 6

    Overexpression of CHK1 and CHK2 in pediatric patients of B-acute lymphoblastic leukemia by Heidari, Farshad, Faranoush, Mohammad, Amini, Ali, Rahimian, Elahe, Kazemi, Kamyar, Paridar, Mostafa, Safa, Majid

    “…Background: Despite breakthroughs in the development of chemotherapy drugs to treat pediatric B-acute lymphoblastic leukemia (B-ALL), the relapse rate remains…”
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  7. 7

    Overexpression of long non-coding RNA ANRIL in B-acute lymphoblastic leukemia by Bahraini, Mehran, Faranoush, Mohammad, Naseri Mobaraki, Sepideh, Paridar, Mostafa, Amini, Ali, Manafi Shabestari, Rima, Safa, Majid

    “…Background: Dysregulation of LncRNA antisense non-coding RNA in the INK4 locus (ANRIL) expression is implicated in pathogenesis and disease progression of a…”
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  8. 8

    Widely distribution of hematological parameters in thalassemia patients with similar α-globin genotype by Keikhaei, Bijan, Salehi-Fard, Pejman, Paridar, Mostafa, Karimzadeh, Mehraneh, Dehghani, Razie, Zamiri, Asma, Takhviji, Vahideh

    Published in Frontiers in biology (01-12-2018)
    “…Background Thalassemia is known as the commonest monogenic disorder with an imbalanced rate of globin chains production of adult hemoglobin. Despite the…”
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  9. 9

    RITA induces apoptosis in p53-null K562 leukemia cells by inhibiting STAT5, Akt, and NF-κB signaling pathways by Mobaraki, Rashideh N, Karimi, Maryam, Alikarami, Fatemeh, Farhadi, Elham, Amini, Ali, Bashash, Davood, Paridar, Mostafa, Kokhaei, Parviz, Rezvani, Mohammad R, Kazemi, Ahmad, Safa, Majid

    Published in Anti-cancer drugs (01-10-2018)
    “…Targeting oncogenic signaling pathways by small molecules has emerged as a potential treatment strategy for cancer. reactivation of p53 and induction of tumor…”
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  10. 10

    Overexpression of MiR-138 Inhibits Cell Growth and Induces Caspase-mediated Apoptosis in Acute Promyelocytic Leukemia Cell Line by Manafi Shabestari, Rima, Alikarami, Fatemeh, Bashash, Davood, Paridar, Mostafa, Safa, Majid

    “…Dysregulated expression of miRNAs can play a vital role in pathogenesis of leukemia. The shortened telomere length, and elevated telomerase activity in acute…”
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  11. 11

    Evaluation of α-Globin Gene Mutations Among Different Ethnic Groups in Khuzestan Province, Southwest Iran by Khosravi, Abbas, Jalali-Far, Mohammadali, Saki, Najmaldin, Hosseini, Hossein, Galehdari, Hamid, Kiani-Ghalesardi, Omid, Paridar, Mostafa, Azarkeivan, Azita, Magaji-Hamid, Kabir

    Published in Hemoglobin (03-03-2016)
    “…α-Thalassemia (α-thal) is one of the most common inherited hemoglobin (Hb) disorders in the world. In addition to large deletions, over 50 different α-thal…”
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  12. 12

    Mobile blood collection sites and their roles in providing safe and adequate supply: A six-year experience by Paridar, Mostafa, Khosravi, Abbas, Jalali-Far, Mohammad-Ali, Zolfaghari, Sima, Ghaleh Sardi, Omid Kiani, Sajadi, Mehdi

    Published in Frontiers in biology (01-06-2018)
    “…Background The determination of the role of mobile sites, as compared with fixed sites, in providing safe blood supply will help with the planning of future…”
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    Journal Article