Search Results - Murphy, Quinn

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  1. 1
    SPEG binds with desmin and its deficiency causes defects in triad and focal adhesion proteins

    SPEG binds with desmin and its deficiency causes defects in triad and focal adhesion proteins by Luo, Shiyu, Li, Qifei, Lin, Jasmine, Murphy, Quinn, Marty, Isabelle, Zhang, Yuanfan, Kazerounian, Shideh, Agrawal, Pankaj B

    Published 2020
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  2. 2
    Electrochemical micro-aptasensors for exosome detection based on hybridization chain reaction amplification

    Electrochemical micro-aptasensors for exosome detection based on hybridization chain reaction amplification by Zhang, Wenfen, Tian, Zhenhua, Yang, Shujie, Rich, Joseph, Zhao, Shuaiguo, Klingeborn, Mikael, Huang, Po-Hsun, Li, Zhishang, Stout, Alexander, Murphy, Quinn, Patz, Edward, Zhang, Shusheng, Liu, Guozhen, Huang, Tony Jun

    Published 2021
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  3. 3
    Transgenic zebrafish model of DUX4 misexpression reveals a developmental role in FSHD pathogenesis

    Transgenic zebrafish model of DUX4 misexpression reveals a developmental role in FSHD pathogenesis by Pakula, Anna, Lek, Angela, Widrick, Jeffrey, Mitsuhashi, Hiroaki, Bugda Gwilt, Katlynn M, Gupta, Vandana A, Rahimov, Fedik, Criscione, June, Zhang, Yuanfan, Gibbs, Devin, Murphy, Quinn, Manglik, Anusha, Mead, Lillian, Kunkel, Louis

    Published 2019
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  4. 4
    Neonatal-Onset Chronic Diarrhea Caused by Homozygous Nonsense WNT2B Mutations

    Neonatal-Onset Chronic Diarrhea Caused by Homozygous Nonsense WNT2B Mutations by O’Connell, Amy E., Zhou, Fanny, Shah, Manasvi S., Murphy, Quinn, Rickner, Hannah, Kelsen, Judith, Boyle, John, Doyle, Jefferson J., Gangwani, Bharti, Thiagarajah, Jay R., Kamin, Daniel S., Goldsmith, Jeffrey D., Richmond, Camilla, Breault, David T., Agrawal, Pankaj B.

    Published 2018
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  5. 5
    De novo variant of TRRAP in a patient with very early onset psychosis in the context of non-verbal learning disability and obsessive-compulsive disorder: a case report

    De novo variant of TRRAP in a patient with very early onset psychosis in the context of non-verbal learning disability and obsessive-compulsive disorder: a case report by Mavros, Chrystal F., Brownstein, Catherine A., Thyagrajan, Roshni, Genetti, Casie A., Tembulkar, Sahil, Graber, Kelsey, Murphy, Quinn, Cabral, Kristin, VanNoy, Grace E., Bainbridge, Matthew, Shi, Jiahai, Agrawal, Pankaj B., Beggs, Alan H., D’Angelo, Eugene, Gonzalez-Heydrich, Joseph

    Published 2018
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  6. 6
    Mammalian Hbs1L deficiency causes congenital anomalies and developmental delay associated with Pelota depletion and 80S monosome accumulation

    Mammalian Hbs1L deficiency causes congenital anomalies and developmental delay associated with Pelota depletion and 80S monosome accumulation by O’Connell, Amy E., Gerashchenko, Maxim V., O’Donohue, Marie-Francoise, Rosen, Samantha M., Huntzinger, Eric, Gleeson, Diane, Galli, Antonella, Ryder, Edward, Cao, Siqi, Murphy, Quinn, Kazerounian, Shideh, Morton, Sarah U., Schmitz-Abe, Klaus, Gladyshev, Vadim N., Gleizes, Pierre-Emmanuel, Séraphin, Bertrand, Agrawal, Pankaj B.

    Published 2019
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