Resultats de la cerca - Yah‐Huei Wu‐Chou

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  1. 1
    Neuroprotective effects of aldehyde dehydrogenase 2 activation in rotenone-induced cellular and animal models of parkinsonism

    Neuroprotective effects of aldehyde dehydrogenase 2 activation in rotenone-induced cellular and animal models of parkinsonism per Ching‐Chi Chiu, Tu‐Hsueh Yeh, Szu‐Chia Lai, Yah‐Huei Wu‐Chou, Che-Hong Chen, Daria Mochly‐Rosen, Yin-Cheng Huang, Yu-Jie Chen, Chao-Lang Chen, Ya-Ming Chang, Hung‐Li Wang, Chin-Song Lu

    Publicat 2014
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  2. 2
    Evidence of gene–environment interaction for the IRF6 gene and maternal multivitamin supplementation in controlling the risk of cleft lip with/without cleft palate

    Evidence of gene–environment interaction for the IRF6 gene and maternal multivitamin supplementation in controlling the risk of cleft lip with/without cleft palate per Tao Wu, Kung Yee Liang, Jacqueline B. Hetmanski, Ingo Ruczinski, Margaret Daniele Fallin, Roxann Ingersoll, Hong Wang, Shangzhi Huang, Xiaoqian Ye, Yah‐Huei Wu‐Chou, Philip K. Chen, Ethylin Wang Jabs, Bing Shi, Richard J. Redett, Alan F. Scott, Terri H. Beaty

    Publicat 2010
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  3. 3
    Association between IRF6 and nonsyndromic cleft lip with or without cleft palate in four populations

    Association between IRF6 and nonsyndromic cleft lip with or without cleft palate in four populations per Ji Wan Park, Iain McIntosh, Jacqueline B. Hetmanski, Ethylin Wang Jabs, Craig A. der Van Kolk, Yah‐Huei Wu‐Chou, Philip K. Chen, Samuel S. Chong, Vincent Yeow, Sun Ha Jee, Beyoung Yun Park, M. Daniele Fallin, Roxann Ingersoll, Alan F. Scott, Terri H. Beaty

    Publicat 2007
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  4. 4
    Whole Exome Sequencing of Distant Relatives in Multiplex Families Implicates Rare Variants in Candidate Genes for Oral Clefts

    Whole Exome Sequencing of Distant Relatives in Multiplex Families Implicates Rare Variants in Candidate Genes for Oral Clefts per Alexandre Bureau, Margaret M. Parker, Ingo Ruczinski, Margaret A. Taub, Mary L. Marazita, Jeffrey C. Murray, Elisabeth Mangold, Markus M. Nöethen, Kirsten U Ludwig, Jacqueline B. Hetmanski, Joan E. Bailey‐Wilson, Cheryl D. Cropp, Qing Li, Silke Szymczak, Hasan Albacha‐Hejazi, Khalid Alqosayer, L. Leigh Field, Yah‐Huei Wu‐Chou, Kimberly F. Doheny, Hua Ling, Alan F. Scott, Terri H. Beaty

    Publicat 2014
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  5. 5
    Genome-wide Enrichment of De Novo Coding Mutations in Orofacial Cleft Trios

    Genome-wide Enrichment of De Novo Coding Mutations in Orofacial Cleft Trios per Madison R. Bishop, Kimberly K. Diaz Perez, Miranda Sun, Samantha Ho, Pankaj Chopra, Nandita Mukhopadhyay, Jacqueline B. Hetmanski, Margaret A. Taub, Lina Moreno‐Uribe, Luz Consuelo Valencia‐Ramirez, Claudia P. Restrepo Muñeton, George L. Wehby, Jacqueline T. Hecht, Frederic W.‐B. Deleyiannis, Seth M. Weinberg, Yah Huei Wu‐Chou, Philip K. Chen, Harrison Brand, Michael P. Epstein, Ingo Ruczinski, Jeffrey C. Murray, Terri H. Beaty, Eleanor Feingold, Robert J. Lipinski, David J. Cutler, Mary L. Marazita, Elizabeth J. Leslie

    Publicat 2020
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  6. 6
    Evidence for gene-environment interaction in a genome wide study of nonsyndromic cleft palate

    Evidence for gene-environment interaction in a genome wide study of nonsyndromic cleft palate per Terri H. Beaty, Ingo Ruczinski, Jeffrey C. Murray, Mary L. Marazita, Ronald G. Munger, Jacqueline B. Hetmanski, Tanda Murray, Richard J. Redett, M. Daniele Fallin, Kung Yee Liang, Tao Wu, Poorav J. Patel, Sheng Chih Jin, Tian Xiao Zhang, Holger Schwender, Yah Huei Wu‐Chou, Philip K. Chen, Samuel S. Chong, Felicia S.H. Cheah, Vincent Yeow, Xiaoqian Ye, Hong Wang, Shangzhi Huang, Ethylin Wang Jabs, Bing Shi, Allen J. Wilcox, Rolv T. Lie, Sun Ha Jee, Kaare Christensen, Kimberley F. Doheny, Elizabeth Pugh, Hua Ling, Alan F. Scott

    Publicat 2011
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  7. 7
    <scp><i>EIF2AK2</i></scp> Missense Variants Associated with Early Onset Generalized Dystonia

    <scp><i>EIF2AK2</i></scp> Missense Variants Associated with Early Onset Generalized Dystonia per Demy J.S. Kuipers, Wim Mandemakers, Chin‐Song Lu, Simone Olgiati, Guido J. Breedveld, Christina Fevga, Vera Tadić, Miryam Carecchio, Bradley Osterman, Lena Sagi‐Dain, Yah‐Huei Wu‐Chou, Chiung C. Chen, Hsiu‐Chen Chang, Shey‐Lin Wu, Tu‐Hsueh Yeh, Yi‐Hsin Weng, Antonio E. Elia, Celeste Panteghini, Nicolas Marotta, Martje G. Pauly, Andrea A. Kühn, Jens Volkmann, Baiba Lāce, Inge A. Meijer, Krishna Kumar Kandaswamy, Marialuisa Quadri, Barbara Garavaglia, Katja Lohmann, Peter Bauer, Niccolò E. Mencacci, Steven Lubbe, Christine Klein, Aida M. Bertoli‐Avella, Vincenzo Bonifati

    Publicat 2020
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  8. 8
    LRP10 genetic variants in familial Parkinson's disease and dementia with Lewy bodies: a genome-wide linkage and sequencing study

    LRP10 genetic variants in familial Parkinson's disease and dementia with Lewy bodies: a genome-wide linkage and sequencing study per Marialuisa Quadri, Wim Mandemakers, Martyna M. Grochowska, Roy Masius, Hanneke Geut, Edito Fabrizio, Guido J. Breedveld, Demy J.S. Kuipers, Michelle Minneboo, Leonie J.M. Vergouw, Ana Carreras Mascaro, Ekaterina Yonova-Doing, Erik Simons, Tianna Zhao, Alessio Di Fonzo, Hsiu‐Chen Chang, Piero Parchi, Marta Melis, Leonor Correia Guedes, Chiara Criscuolo, Astrid Thomas, Rutger W. W. Brouwer, Daphne Heijsman, Angela Ingrassia, Giovanna Calandra‐Buonaura, Janneke P.A Rood, Sabina Capellari, Annemieke J.M. Rozemüller, Marianna Sarchioto, Hsin Fen Chien, Nicola Vanacore, Simone Olgiati, Yah-Huei Wu-Chou, Tu‐Hsueh Yeh, Agnita J.W. Boon, Susanne E. Hoogers, Mehrnaz Ghazvini, Arne IJpma, Wilfred F. J. van IJcken, Marco Onofrj, Paolo Barone, David Nicholl, Andreas Puschmann, Michele De Mari, Anneke J.A. Kievit, Egberto Reis Barbosa, Giuseppe De Michele, Daniëlle Majoor‐Krakauer, John C. van Swieten, Frank Jan de Jong, Joaquim J. Ferreira, Giovanni Cossu, Chin‐Song Lu, G. Meco, Pietro Cortelli, Wilma D.J. van de Berg, Vincenzo Bonifati, Vincenzo Bonifati, Marialuisa Quadri, Wim Mandemakers, Anneke J.A. Kievit, Agnita J.W. Boon, Janneke P.A Rood, Leonie J.M. Vergouw, Frank Jan de Jong, John C. van Swieten, Francesco Mattace‐Raso, Klaus L. Leenders, Joaquim J. Ferreira, Leonor Correia Guedes, Andreas Puschmann, Emil Ygland, Christer Nilsson, Hsin Fen Chien, Egberto Reis Barbosa, Laura Bannach Jardim, Carlos Roberto de Mello Rieder, Hsiu‐Chen Chang, Chin‐Song Lu, Yah-Huei Wu-Chou, Tu‐Hsueh Yeh, Leonardo Lopiano, Cristina Tassorelli, C. Pacchetti, Giulio Riboldazzi, Giorgio Bono, Cristoforo Comi, Alessandro Padovani, Barbara Borroni, Francesco Raudino, E. Fincati, Michèle Tinazzi, A. Bonizzato, C Ferracci, A. Dalla Libera, Giovanni Abbruzzese, Pietro Cortelli, Sabina Capellari, Roberto Marconi, Marco Guidi

    Publicat 2018
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  9. 9
    A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4

    A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4 per Terri H. Beaty, Jeffrey C. Murray, Mary L. Marazita, Ronald G. Munger, Ingo Ruczinski, Jacqueline B. Hetmanski, Kung Yee Liang, Tao Wu, Tanda Murray, M. Daniele Fallin, Richard Redett, Gerald V. Raymond, Holger Schwender, Sheng Chih Jin, Margaret E. Cooper, Martine Dunnwald, M. Adela Mansilla, Elizabeth J. Leslie, Stephen Bullard, Andrew C. Lidral, Lina M. Moreno, Renato Menezes, Alexandre R. Vieira, Aline Petrin, Allen J. Wilcox, Rolv T. Lie, Ethylin Wang Jabs, Yah Huei Wu‐Chou, Philip K. Chen, Hong Wang, Xiaoqian Ye, Shangzhi Huang, Vincent Yeow, Samuel S. Chong, Sun Ha Jee, Bing Shi, Kaare Christensen, Mads Melbye, Kimberly F. Doheny, Elizabeth Pugh, Hua Ling, Eduardo E. Castilla, Andrew E. Czeizel, Lian Ma, L. Leigh Field, Lawrence C. Brody, Faith Pangilinan, James L. Mills, Anne M. Molloy, Peadar N. Kirke, John M. Scott, Mauricio Arcos‐Burgos, Alan F. Scott

    Publicat 2010
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  10. 10
    Erratum: A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4

    Erratum: A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4 per Terri H. Beaty, Jeffrey C. Murray, Mary L. Marazita, Ronald G. Munger, Ingo Ruczinski Jacqueline B Hetmanski, Kung Yee Liang, Tao Wu, Tanda Murray, M. Daniele Fallin, Richard Redett, Gerald V. Raymond, Holger Schwender, Shin C Jin, Margaret E. Cooper, Martine Dunnwald, M. Adela Mansilla, Elizabeth J. Leslie, Stephen Bullard, Andrew C. Lidral, Lina M. Moreno, Renato Menezes, Alexandre R. Vieira, Aline Petrin, Allen J. Wilcox, Rolv T. Lie, Ethylin Wang Jabs, Yah Huei Wu‐Chou, Philip K. Chen, Hong Wang, Xiaoqian Ye, Shangzhi Huang, Vincent Yeow, Samuel S. Chong, Sun Ha Jee, Bing Shi, Kaare Christensen, Mads Melbye, Kimberly F. Doheny, Elizabeth Pugh, Hua Ling, Eduardo E. Castilla, Andrew E. Czeizel, Lian Ma, L. Leigh Field, Lawrence C. Brody, Faith Pangilinan, James L. Mills, Anne M. Molloy, Peadar N. Kirke, James M Scott, Mauricio Arcos‐Burgos, Alan F. Scott

    Publicat 2010
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