Extracellular signal-regulated kinase 1 and 2 in cancer therapy: a focus on hepatocellular carcinoma von Mehdizadeh, Amir, Somi, Mohammad Hossein, Darabi, Masoud, Jabbarpour-Bonyadi, Mortaza

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R229Q Polymorphism of NPHS2 Gene in Patients With Late-Onset Steroid-Resistance Nephrotic Syndrome: A Preliminary Study von Fotouhi, Nikou, Ardalan, Mohammadreza, Bonyadi, Mortaza Jabbarpour, Abdolmohammadi, Reza, Kamalifar, Amir, Nasri, Hamid, Einollahi, Behzad

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A novel loss of function mutation in the PHD domain of the RAG2 gene, affecting zinc-binding affinity von Jabbarpour, Neda, Bonyadi, Mortaza, Sadeghi, Leila

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Giant axonal neuropathy: a rare inherited neuropathy with a novel mutation von Poorshiri, Bita, Jabbarpour, Neda, Barzegar, Mohammad, Bonyadi, Mortaza, Ebadi, Zakiyeh

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Identification of Two Novel Pathogenic Variants of the ATM Gene in the Iranian-Azeri Turkish Ethnic Group by Applying Whole Exome Sequencing von Amandi, Amir-Reza Dalal, Jabbarpour, Neda, Shiva, Shadi, Bonyadi, Mortaza

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Identification of a novel mutation in the HACD1 gene in an Iranian family with autosomal recessive congenital myopathy, with fibre-type disproportion von Jabbarpour, Neda, Poorshiri, Bita, Saei, Hassan, Barzegar, Mohammad, Bonyadi, Mortaza

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Identification of a de novo, Novel Pathogenic Variant in the Splice Region of the SOX10 Gene in an Iranian Azeri Turkish Family with Waardenburg Syndrome von Roudbari, Faranak, Dallal Amandi, Amir-Reza, Bonyadi, Mortaza, Sadeghi, Leyla, Jabbarpour, Neda

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Association of CFI p.Gly119Arg gene polymorphism with age-related macular degeneration (AMD) disease in the population living in Tehran von Neda Norouzi, Mortaza Bonyadi, Esmaeil Babaei, Mohammad Hossein Jabbarpour Bonyadi

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Association of CFI gene polymorphism with age related macular degeneration in Northwest of Iran von norouzi, neda, Bonyadi, Mortaza, Babaei, Esmaeil, Jabbarpour Bonyadi, Mohammad Hossein, Javadzadeh, AliReza

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