Search Results - Rezaei, Majdaddin

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  1. 1
    Lack of Evidence of the Role of APOA5 3'UTR Polymorphisms in Iranian Children and Adolescents with Metabolic Syndrome

    Lack of Evidence of the Role of APOA5 3'UTR Polymorphisms in Iranian Children and Adolescents with Metabolic Syndrome by Salehi, Samaneh, Emadi-Baygi, Modjtaba, Rezaei, Majdaddin, Kelishadi, Roya, Nikpour, Parvaneh

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  2. 2
    Identification of a New Single-nucleotide Polymorphism within the Apolipoprotein A5 Gene, Which is Associated with Metabolic Syndrome

    Identification of a New Single-nucleotide Polymorphism within the Apolipoprotein A5 Gene, Which is Associated with Metabolic Syndrome by Salehi, Samaneh, Emadi-Baygi, Modjtaba, Rezaei, Majdaddin, Kelishadi, Roya, Nikpour, Parvaneh

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  3. 3
    Lack of Evidence of the Role of 3’UTR Polymorphisms in Iranian Children and Adolescents with Metabolic Syndrome

    Lack of Evidence of the Role of 3’UTR Polymorphisms in Iranian Children and Adolescents with Metabolic Syndrome by Samaneh Salehi, Modjtaba Emadi-Baygi, Majdaddin Rezaei, Roya Kelishadi, Parvaneh Nikpour

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  4. 4
    In vivo interrogation of regulatory genomes reveals extensive quasi-insufficiency in cancer evolution

    In vivo interrogation of regulatory genomes reveals extensive quasi-insufficiency in cancer evolution by Fischer, Anja, Lersch, Robert, de Andrade Krätzig, Niklas, Strong, Alexander, Friedrich, Mathias J., Weber, Julia, Engleitner, Thomas, Öllinger, Rupert, Yen, Hsi-Yu, Kohlhofer, Ursula, Gonzalez-Menendez, Irene, Sailer, David, Kogan, Liz, Lahnalampi, Mari, Laukkanen, Saara, Kaltenbacher, Thorsten, Klement, Christine, Rezaei, Majdaddin, Ammon, Tim, Montero, Juan J., Schneider, Günter, Mayerle, Julia, Heikenwälder, Mathias, Schmidt-Supprian, Marc, Quintanilla-Martinez, Leticia, Steiger, Katja, Liu, Pentao, Cadiñanos, Juan, Vassiliou, George S., Saur, Dieter, Lohi, Olli, Heinäniemi, Merja, Conte, Nathalie, Bradley, Allan, Rad, Lena, Rad, Roland

    Published in Cell genomics
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  5. 5
    Lack of Evidence of the Role of APOA5 3’UTR Polymorphisms in Iranian Children and Adolescents with Metabolic Syndrome

    Lack of Evidence of the Role of APOA5 3’UTR Polymorphisms in Iranian Children and Adolescents with Metabolic Syndrome by Samaneh Salehi, Modjtaba Emadi-baygi, Majdaddin Rezaei, Roya Kelishadi, Parvaneh Nikpour

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