Search Results - Ramshe, Samira Molaei

  • Showing 1 - 9 results of 9
Refine Results
  1. 1
    A Novel Ornithine Aminotransferase Splice Site Mutation Causes Vitamin B6-Responsive Gyrate Atrophy

    A Novel Ornithine Aminotransferase Splice Site Mutation Causes Vitamin B6-Responsive Gyrate Atrophy by Molaei Ramshe, Samira, Zardadi, Safoura, Alehabib, Elham, Nourinia, Ramin, Jamshidi, Javad, Soosanabadi, Mohsen, Darvish, Hossein

    Get full text
    Items that this one cites
    Article
    Save to List
    Saved in:
  2. 2
    Up-regulation of FOXN3-AS1 in invasive ductal carcinoma of breast cancer patients

    Up-regulation of FOXN3-AS1 in invasive ductal carcinoma of breast cancer patients by Molaei Ramshe, Samira, Ghaedi, Hamid, Omrani, Mir Davood, Geranpayeh, Lobat, Alipour, Behnam, Ghafouri-Fard, Soudeh

    Published in Heliyon
    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  3. 3
    Cancer exosomes and natural killer cells dysfunction: biological roles, clinical significance and implications for immunotherapy

    Cancer exosomes and natural killer cells dysfunction: biological roles, clinical significance and implications for immunotherapy by Hosseini, Reza, Sarvnaz, Hamzeh, Arabpour, Maedeh, Ramshe, Samira Molaei, Asef-Kabiri, Leila, Yousefi, Hassan, Akbari, Mohammad Esmaeil, Eskandari, Nahid

    Published in Molecular cancer
    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  4. 4
    IGF family effects on development, stability, and treatment of hematological malignancies

    IGF family effects on development, stability, and treatment of hematological malignancies by Moonesi, Mohammadreza, Zaka Khosravi, Saeed, Molaei Ramshe, Samira, Allahbakhshian Farsani, Mehdi, Solali, Saeed, Mohammadi, Mohammad Hossein, Farshdousti Hagh, Majid, Mehdizadeh, Hanie

    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  5. 5
    Leu226Trp CACNA1A variant associated with juvenile myoclonic epilepsy with and without intellectual disability

    Leu226Trp CACNA1A variant associated with juvenile myoclonic epilepsy with and without intellectual disability by Alehabib, Elham, Kokotović, Tomislav, Ranji-Burachaloo, Sakineh, Tafakhori, Abbas, Ramshe, Samira Molaei, Esmaeilizadeh, Zahra, Darvish, Hossein, Movafagh, Abolfazl, Nagy, Vanja

    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  6. 6
    An overview of the molecular and clinical significance of the angiopoietin system in leukemia

    An overview of the molecular and clinical significance of the angiopoietin system in leukemia by Zaka Khosravi, Saeed, Molaei Ramshe, Samira, Allahbakhshian Farsani, Mehdi, Moonesi, Mohammadreza, Marofi, Faroogh, Hagh, Majid Farshdousti

    Get full text
    Items that this one cites
    Article
    Save to List
    Saved in:
  7. 7
    Investigating the expression pattern of the angiopoietin-Tie system in ALL and its correlation with baseline characteristics

    Investigating the expression pattern of the angiopoietin-Tie system in ALL and its correlation with baseline characteristics by Khosravi, Saeed Zaka, Ramshe, Samira Molaei, Farsani, Mehdi Allahbakhshian, Solali, Saeed, Moonesi, Mohammadreza, Hagh, Majid Farshdousti

    Published in Blood research
    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  8. 8
    ZSCAN10 deficiency causes a neurodevelopmental disorder with characteristic oto-facial malformations

    ZSCAN10 deficiency causes a neurodevelopmental disorder with characteristic oto-facial malformations by Laugwitz, Lucia, Cheng, Fubo, Collins, Stephan C, Hustinx, Alexander, Navarro, Nicolas, Welsch, Simon, Cox, Helen, Hsieh, Tzung-Chien, Vijayananth, Aswinkumar, Buchert, Rebecca, Bender, Benjamin, Efthymiou, Stephanie, Murphy, David, Zafar, Faisal, Rana, Nuzhat, Grasshoff, Ute, Falb, Ruth J, Grimmel, Mona, Seibt, Annette, Zheng, Wenxu, Ghaedi, Hamid, Thirion, Marie, Couette, Sébastien, Azizimalamiri, Reza, Sadeghian, Saeid, Galehdari, Hamid, Zamani, Mina, Zeighami, Jawaher, Sedaghat, Alireza, Ramshe, Samira Molaei, Zare, Ali, Alipoor, Behnam, Klee, Dirk, Sturm, Marc, Ossowski, Stephan, Houlden, Henry, Riess, Olaf, Wieczorek, Dagmar, Gavin, Ryan, Maroofian, Reza, Krawitz, Peter, Yalcin, Binnaz, Distelmaier, Felix, Haack, Tobias B

    Get full text
    Items that this one cites
    Article
    Save to List
    Saved in:
  9. 9
    A Novel Ornithine Aminotransferase Splice Site Mutation Causes Vitamin B6-Responsive Gyrate Atrophy

    A Novel Ornithine Aminotransferase Splice Site Mutation Causes Vitamin B6-Responsive Gyrate Atrophy by Molaei Ramshe, Samira, Zardadi, Safoura, Alehabib, Elham, Nourinia, Ramin, Jamshidi, Javad, Soosanabadi, Mohsen, Darvish, Hossein

    Get full text
    Report
    Save to List
    Saved in:

Search Tools: