Search Results - Fardaei, M.

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  1. 1
    Three proteins, MBNL, MBLL and MBXL, co-localize in vivo with nuclear foci of expanded-repeat transcripts in DM1 and DM2 cells

    Three proteins, MBNL, MBLL and MBXL, co-localize in vivo with nuclear foci of expanded-repeat transcripts in DM1 and DM2 cells by Fardaei, Majid, Rogers, Mark T., Thorpe, Helena M., Larkin, Kenneth, Hamshere, Marion G., Harper, Peter S., Brook, J. David

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  2. 2
    In vivo co-localisation of MBNL protein with DMPK expanded-repeat transcripts

    In vivo co-localisation of MBNL protein with DMPK expanded-repeat transcripts by Fardaei, M, Larkin, K, Brook, J D, Hamshere, M G

    Published in Nucleic acids research
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  3. 3
    Genetic variations of 21 STR markers on chromosomes 13, 18, 21, X, and Y in the south Iranian population

    Genetic variations of 21 STR markers on chromosomes 13, 18, 21, X, and Y in the south Iranian population by Saberzadeh, J, Miri, M R, Tabei, M B, Dianatpour, M, Fardaei, M

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  4. 4
    Construction of bacterial ghosts for transfer and expression of a chimeric hepatitis C virus gene in macrophages

    Construction of bacterial ghosts for transfer and expression of a chimeric hepatitis C virus gene in macrophages by Miri, M.R., Behzad-Behbahani, A., Fardaei, M., Farhadi, A., Talebkhan, Y., Mohammadi, M., Tayebinia, M., Farokhinejad, F., Alavi, P., Fanian, M., Zare, F., Saberzade, J., Nikouyan, N., Okhovat, M.A., Ranjbaran, R., Rafiei Dehbidi, G., Naderi, S.

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  5. 5
    D.P.4.10 Muscleblind-like proteins: Similarities and differences in normal and myotonic dystrophy muscle

    D.P.4.10 Muscleblind-like proteins: Similarities and differences in normal and myotonic dystrophy muscle by Holt, I, Furling, D, Fardaei, M, Sewry, C.A, Jacquemin, V, Butler-Browne, G.S, Brook, J.D, Morris, G.E

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  6. 6
    Molecular Mechanism of Myotonic Dystrophy: RNA Gain-of-Function

    Molecular Mechanism of Myotonic Dystrophy: RNA Gain-of-Function by Fardaei, M, Farajzadeh, N

    Published in Cell journal (Yakhteh)
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  7. 7
    Myotonic dystrophy: A multigene disorder

    Myotonic dystrophy: A multigene disorder by LARKIN, Ken, FARDAEI, Majid

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  8. 8
    Family screening for a novel ATP7B gene mutation, c.2335T>G, in the South of Iran

    Family screening for a novel ATP7B gene mutation, c.2335T>G, in the South of Iran by Manoochehri, J, Masoumi Dehshiri, R, Faraji, H, Mohammadi, S, Dastsooz, H, Moradi, T, Rezaei, E, Sadeghi, Kh, Fardaei, M

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  9. 9
    Inferior Spear-like Lens Opacity as a Sign of Keratoconus

    Inferior Spear-like Lens Opacity as a Sign of Keratoconus by Salouti, Ramin, Khosravi, Amir, Fardaei, Majid, Zamani, Mohammad, Nejabat, Mahmoud, Ghoreyshi, Maryam, Yazdanpanah, Mahboobeh, Salouti, Kia, Nowroozzadeh, M Hossein

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  10. 10
    The genomic architecture of NLRP7 is Alu rich and predisposes to disease-associated large deletions

    The genomic architecture of NLRP7 is Alu rich and predisposes to disease-associated large deletions by Reddy, Ramesh, Nguyen, Ngoc M P, Sarrabay, Guillaume, Rezaei, Maryam, Rivas, Mayra C G, Kavasoglu, Aysenur, Berkil, Hakan, Elshafey, Alaa, Abdalla, Ebtesam, Nunez, Kristin P, Dreyfus, Hélène, Philippe, Merviel, Hadipour, Zahra, Durmaz, Asude, Eaton, Erin E, Schubert, Brittany, Ulker, Volkan, Hadipour, Fatemeh, Ahmadpour, Fatemeh, Touitou, Isabelle, Fardaei, Majid, Slim, Rima

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  11. 11
    The genomic architecture of NLRP7 is Alu rich and predisposes to disease-associated large deletions

    The genomic architecture of NLRP7 is Alu rich and predisposes to disease-associated large deletions by Reddy, Ramesh, Nguyen, Ngoc M P, Sarrabay, Guillaume, Rezaei, Maryam, Rivas, Mayra C G, Kavasoglu, Aysenur, Berkil, Hakan, Elshafey, Alaa, Abdalla, Ebtesam, Nunez, Kristin P, Dreyfus, Hélène, Philippe, Merviel, Hadipour, Zahra, Durmaz, Asude, Eaton, Erin E, Schubert, Brittany, Ulker, Volkan, Hadipour, Fatemeh, Touitou, Isabelle, Fardaei, Majid, Slim, Rima

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  12. 12
    Erratum: The genomic architecture of NLRP7 is Alu rich and predisposes to disease-associated large deletions

    Erratum: The genomic architecture of NLRP7 is Alu rich and predisposes to disease-associated large deletions by Reddy, Ramesh, Nguyen, Ngoc M P, Sarrabay, Guillaume, Rezaei, Maryam, Rivas, Mayra C G, Kavasoglu, Aysenur, Berkil, Hakan, Elshafey, Alaa, Abdalla, Ebtesam, Nunez, Kristin P, Dreyfus, Hélène, Philippe, Merviel, Hadipour, Zahra, Durmaz, Asude, Eaton, Erin E, Schubert, Brittany, Ulker, Volkan, Hadipour, Fatemeh, Touitou, Isabelle, Fardaei, Majid, Slim, Rima

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