Search Results - "Fuentes, Daniel R."

Systematic perturbation of retroviral LTRs reveals widespread long-range effects on human gene regulation by Fuentes, Daniel R, Swigut, Tomek, Wysocka, Joanna

“…Recent work suggests extensive adaptation of transposable elements (TEs) for host gene regulation. However, high numbers of integrations typical of TEs,…”
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Hierarchical Mechanisms for Direct Reprogramming of Fibroblasts to Neurons by Wapinski, Orly L., Vierbuchen, Thomas, Qu, Kun, Lee, Qian Yi, Chanda, Soham, Fuentes, Daniel R., Giresi, Paul G., Ng, Yi Han, Marro, Samuele, Neff, Norma F., Drechsel, Daniela, Martynoga, Ben, Castro, Diogo S., Webb, Ashley E., Südhof, Thomas C., Brunet, Anne, Guillemot, Francois, Chang, Howard Y., Wernig, Marius

“…Direct lineage reprogramming is a promising approach for human disease modeling and regenerative medicine, with poorly understood mechanisms. Here, we reveal a…”
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Induction of human neuronal cells by defined transcription factors by Pang, Zhiping P., Yang, Nan, Vierbuchen, Thomas, Ostermeier, Austin, Fuentes, Daniel R., Yang, Troy Q., Citri, Ami, Sebastiano, Vittorio, Marro, Samuele, Südhof, Thomas C., Wernig, Marius

“…Neurons from fibroblasts Three papers in this issue demonstrate the production of functional induced neuronal (iN) cells from human fibroblasts, a procedure…”
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Inappropriate p53 activation during development induces features of CHARGE syndrome by Van Nostrand, Jeanine L., Brady, Colleen A., Jung, Heiyoun, Fuentes, Daniel R., Kozak, Margaret M., Johnson, Thomas M., Lin, Chieh-Yu, Lin, Chien-Jung, Swiderski, Donald L., Vogel, Hannes, Bernstein, Jonathan A., Attié-Bitach, Tania, Chang, Ching-Pin, Wysocka, Joanna, Martin, Donna M., Attardi, Laura D.

“…Inappropriate activation of the tumour-suppressor protein p53 during development can promote phenotypes similar to those of CHARGE syndrome, suggesting that…”
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Author Correction: Myt1l safeguards neuronal identity by actively repressing many non-neuronal fates by Mall, Moritz, Kareta, Michael S., Chanda, Soham, Ahlenius, Henrik, Perotti, Nicholas, Zhou, Bo, Grieder, Sarah D., Ge, Xuecai, Drake, Sienna, Ang, Cheen Euong, Walker, Brandon M., Vierbuchen, Thomas, Fuentes, Daniel R., Brennecke, Philip, Nitta, Kazuhiro R., Jolma, Arttu, Steinmetz, Lars M., Taipale, Jussi, Südhof, Thomas C., Wernig, Marius

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Myt1l safeguards neuronal identity by actively repressing many non-neuronal fates by Mall, Moritz, Kareta, Michael S., Chanda, Soham, Ahlenius, Henrik, Perotti, Nicholas, Zhou, Bo, Grieder, Sarah D., Ge, Xuecai, Drake, Sienna, Euong Ang, Cheen, Walker, Brandon M., Vierbuchen, Thomas, Fuentes, Daniel R., Brennecke, Philip, Nitta, Kazuhiro R., Jolma, Arttu, Steinmetz, Lars M., Taipale, Jussi, Südhof, Thomas C., Wernig, Marius

“…The neuron-specific transcription factor Myt1l represses many somatic lineage programs, but not the neuronal lineage program, to both induce and maintain…”
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Hierarchical mechanisms for transcription factor-mediated reprogramming of fibroblasts to neurons by Wapinski, Orly L., Vierbuchen, Thomas, Qu, Kun, Lee, Qian Yi, Chanda, Soham, Fuentes, Daniel R., Giresi, Paul G., Ng, Yi Han, Marro, Samuele, Neff, Norma F., Drechsel, Daniela, Martynoga, Ben, Castro, Diogo S., Webb, Ashley E., Brunet, Anne, Guillemot, Francois, Chang, Howard Y., Wernig, Marius

“…Direct lineage reprogramming is a promising approach for human disease modeling and regenerative medicine with poorly understood mechanisms. Here we reveal a…”
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