Search Results - Alshamekh, Shomoukh

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  1. 1
    Novel Regulatory Mechanisms for the SoxC Transcriptional Network Required for Visual Pathway Development

    Novel Regulatory Mechanisms for the SoxC Transcriptional Network Required for Visual Pathway Development by Chang, Kun-Che, Hertz, Jonathan, Zhang, Xiong, Jin, Xiao-Lu, Shaw, Peter, Derosa, Brooke A, Li, Janet Y, Venugopalan, Praseeda, Valenzuela, Daniel A, Patel, Roshni D, Russano, Kristina R, Alshamekh, Shomoukh A, Sun, Catalina, Tenerelli, Kevin, Li, Chenyi, Velmeshev, Dmitri, Cheng, Yuyan, Boyce, Timothy M, Dreyfuss, Alexandra, Uddin, Mohammed S, Muller, Kenneth J, Dykxhoorn, Derek M, Goldberg, Jeffrey L

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  2. 2
    Autozygome sequencing expands the horizon of human knockout research and provides novel insights into human phenotypic variation

    Autozygome sequencing expands the horizon of human knockout research and provides novel insights into human phenotypic variation by Alsalem, Ahmed B, Halees, Anason S, Anazi, Shamsa, Alshamekh, Shomoukh, Alkuraya, Fowzan S

    Published in PLoS genetics
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  3. 3
    Infantile Hemangioma of the Breast: Long-Term Assessment of Outcomes

    Infantile Hemangioma of the Breast: Long-Term Assessment of Outcomes by Labow, Brian I, Alshamekh, Shomoukh A, Carlberg, Valerie M, Zacur, Jennifer L, Uihlein, Lily C, Mulliken, John B, Liang, Marilyn G

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  4. 4
    Itch-related quality of life impact across 3 autoimmune blistering diseases: a retrospective cohort study

    Itch-related quality of life impact across 3 autoimmune blistering diseases: a retrospective cohort study by Cole, Emily F., DeGrazia, Taryn, AlShamekh, Shomoukh, Feldman, Ron

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  5. 5
    Autozygome Sequencing Expands the Horizon of Human Knockout Research and Provides Novel Insights into Human Phenotypic Variation: e1004030

    Autozygome Sequencing Expands the Horizon of Human Knockout Research and Provides Novel Insights into Human Phenotypic Variation: e1004030 by Alsalem, Ahmed B, Halees, Anason S, Anazi, Shamsa, Alshamekh, Shomoukh, Alkuraya, Fowzan S

    Published in PLoS genetics
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