نتائج البحث - Sung‐Kook Hong

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  1. 1
    FGF-dependent left–right asymmetry patterning in zebrafish is mediated by Ier2 and Fibp1

    FGF-dependent left–right asymmetry patterning in zebrafish is mediated by Ier2 and Fibp1 حسب Sung‐Kook Hong, Igor B. Dawid

    منشور في 2009
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  2. 2
    The zebrafish <i>kohtalo/trap230</i> gene is required for the development of the brain, neural crest, and pronephric kidney

    The zebrafish <i>kohtalo/trap230</i> gene is required for the development of the brain, neural crest, and pronephric kidney حسب Sung‐Kook Hong, Caroline E. Haldin, Nathan D. Lawson, Brant M. Weinstein, Igor B. Dawid, Neil A. Hukriede

    منشور في 2005
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  3. 3
    Lhx1 Is Required for Specification of the Renal Progenitor Cell Field

    Lhx1 Is Required for Specification of the Renal Progenitor Cell Field حسب M. Cecilia Cirio, Hui Zhao, Caroline E. Haldin, Chiara Cosentino, Carsten Stuckenholz, Xiongfong Chen, Sung‐Kook Hong, Igor B. Dawid, Neil A. Hukriede

    منشور في 2011
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    Artigo
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  4. 4
    An Ultraconserved Brain-Specific Enhancer Within ADGRL3 (LPHN3) Underpins Attention-Deficit/Hyperactivity Disorder Susceptibility

    An Ultraconserved Brain-Specific Enhancer Within ADGRL3 (LPHN3) Underpins Attention-Deficit/Hyperactivity Disorder Susceptibility حسب Ariel F. Martinez, Yu Abe, Sung‐Kook Hong, Kevin Molyneux, David Yarnell, Heiko Löhr, Wolfgang Driever, Maria T. Acosta, Mauricio Arcos‐Burgos, Maximilian Muenke

    منشور في 2016
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    Artigo
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  5. 5
    A CCR4-NOT Transcription Complex, Subunit 1, CNOT1, Variant Associated with Holoprosencephaly

    A CCR4-NOT Transcription Complex, Subunit 1, CNOT1, Variant Associated with Holoprosencephaly حسب Paul Kruszka, Seth Berger, Karin Weiss, Joshua L. Everson, Ariel F. Martinez, Sung‐Kook Hong, Kwame Anyane‐Yeboa, Robert J. Lipinski, Maximilian Muenke

    منشور في 2019
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    Artigo
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  6. 6
    Dominant-negative kinase domain mutations in<i>FGFR1</i>can explain the clinical severity of Hartsfield syndrome

    Dominant-negative kinase domain mutations in<i>FGFR1</i>can explain the clinical severity of Hartsfield syndrome حسب Sung‐Kook Hong, Ping Hu, Juliana Marino, Sophia B. Hufnagel, Robert J. Hopkin, Alma Toromanović, Antônio Richieri‐Costa, Lucilene Arilho Ribeiro, Paul Kruszka, Erich Roessler, Maximilian Muenke

    منشور في 2016
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    Artigo
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  7. 7
    Unique Alterations of an Ultraconserved Non-Coding Element in the 3′UTR of ZIC2 in Holoprosencephaly

    Unique Alterations of an Ultraconserved Non-Coding Element in the 3′UTR of ZIC2 in Holoprosencephaly حسب Erich Roessler, Ping Hu, Sung‐Kook Hong, Kshitij Srivastava, Blake Carrington, Raman Sood, Hanna M. Petrykowska, Laura Elnitski, Lucilene Arilho Ribeiro, Antônio Richieri‐Costa, Benjamin Feldman, Ward F. Odenwald, Maximilian Muenke

    منشور في 2012
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    Artigo
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  8. 8
    Analysis of Upstream Elements in the HuC Promoter Leads to the Establishment of Transgenic Zebrafish with Fluorescent Neurons

    Analysis of Upstream Elements in the HuC Promoter Leads to the Establishment of Transgenic Zebrafish with Fluorescent Neurons حسب Hae‐Chul Park, Cheol‐Hee Kim, Young‐Ki Bae, Sang‐Yeob Yeo, Seok-Hyung Kim, Sung‐Kook Hong, Jimann Shin, Kyeong‐Won Yoo, Masahiko Hibi, Toshio Hirano, Naomasa Miki, Ajay Chitnis, Tae‐Lin Huh

    منشور في 2000
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    Artigo
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  9. 9
    Common genetic causes of holoprosencephaly are limited to a small set of evolutionarily conserved driver genes of midline development coordinated by TGF-β, hedgehog, and FGF signaling

    Common genetic causes of holoprosencephaly are limited to a small set of evolutionarily conserved driver genes of midline development coordinated by TGF-β, hedgehog, and FGF signal... حسب Erich Roessler, Ping Hu, Juliana Marino, Sung‐Kook Hong, Rachel Hart, Seth Berger, Ariel F. Martinez, Yu Abe, Paul Kruszka, James W. Thomas, James C. Mullikin, Yupeng Wang, Wendy S.W. Wong, John E. Niederhuber, Benjamin D. Solomon, Antônio Richieri‐Costa, Lucilene Arilho Ribeiro, Maximilian Muenke

    منشور في 2018
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    Artigo
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