Ngā hua rapu - Miho Ishida

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  1. 1
    The role of imprinted genes in humans

    The role of imprinted genes in humans mā Miho Ishida, Gudrun E. Moore

    I whakaputaina 2012
    Whiwhi kuputuhi katoa
    Revisão
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  2. 2
    Chondroitin 4-O-Sulfotransferase-1 Modulates Wnt-3a Signaling through Control of E Disaccharide Expression of Chondroitin Sulfate

    Chondroitin 4-O-Sulfotransferase-1 Modulates Wnt-3a Signaling through Control of E Disaccharide Expression of Chondroitin Sulfate mā Satomi Nadanaka, Miho Ishida, Masami Ikegami, Hiroshi Kitagawa

    I whakaputaina 2008
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  3. 3
    Chondroitin 4-O-Sulfotransferase-1 Regulates E Disaccharide Expression of Chondroitin Sulfate Required for Herpes Simplex Virus Infectivity

    Chondroitin 4-O-Sulfotransferase-1 Regulates E Disaccharide Expression of Chondroitin Sulfate Required for Herpes Simplex Virus Infectivity mā Toru Uyama, Miho Ishida, Tomomi Izumikawa, Edward Trybala, Frank Tufaro, Tomas Bergström, Kazuyuki Sugahara, Hiroshi Kitagawa

    I whakaputaina 2006
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  4. 4
    Multiple Congenital Melanocytic Nevi and Neurocutaneous Melanosis Are Caused by Postzygotic Mutations in Codon 61 of NRAS

    Multiple Congenital Melanocytic Nevi and Neurocutaneous Melanosis Are Caused by Postzygotic Mutations in Codon 61 of NRAS mā Veronica A. Kinsler, Anna Thomas, Miho Ishida, Neil Bulstrode, Sam Loughlin, Sandra Hing, Jane Chalker, Kathryn J. McKenzie, Sayeda Abu‐Amero, Olga Slater, Estelle Chanudet, Rodger Palmer, Deborah Morrogh, Philip Stanier, Eugene Healy, Neil J. Sebire, Gudrun E. Moore

    I whakaputaina 2013
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  5. 5
    The transcriptomic landscape of monosomy X (45,X) during early human fetal and placental development

    The transcriptomic landscape of monosomy X (45,X) during early human fetal and placental development mā Jenifer P. Suntharalingham, Ignacio del Valle, Federica Buonocore, Sinead McGlacken‐Byrne, Tony Brooks, Olumide Ogunbiyi, Danielle Liptrot, Nathan Dunton, Gaganjit K. Madhan, Kate B. Metcalfe, Lydia Nel, Abigail R. Marshall, Miho Ishida, Neil J. Sebire, Gudrun E. Moore, Berta Crespo, Nita Solanky, Gerard S. Conway, John C. Achermann

    I whakaputaina 2025
    Whiwhi kuputuhi katoa
    Artigo
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  6. 6
    The role and interaction of imprinted genes in human fetal growth

    The role and interaction of imprinted genes in human fetal growth mā Gudrun E. Moore, Miho Ishida, Charalambos Demetriou, Lara Al-Olabi, Lydia J. Leon, Anna Thomas, Sayeda Abu‐Amero, Jennifer M. Frost, Jaime L. Stafford, Chaoqun Yao, Andrew Duncan, Rachel Baigel, Marina Brimioulle, Isabel Iglesias‐Platas, Sophia Apostolidou, Reena Aggarwal, John C. Whittaker, Argyro Syngelaki, K. H. Nicolaides, Lesley Regan, David Monk, Philip Stanier

    I whakaputaina 2015
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Revisão
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  7. 7
    Genetic Analyses in Small-for-Gestational-Age Newborns

    Genetic Analyses in Small-for-Gestational-Age Newborns mā Susanne E. Stalman, Nita Solanky, Miho Ishida, Cristina Alemán-Charlet, Sayeda Abu‐Amero, Mariëlle Alders, Lucas Alvizi, William Baird, Charalambos Demetriou, Peter Henneman, Chela James, Lia Knegt, Lydia J. Leon, Marcel M.A.M. Mannens, Adi N Mul, Nicole A Nibbering, Emma Peskett, Faisal I. Rezwan, Carrie Ris‐Stalpers, Joris van der Post, Gerdine A. Kamp, Frans B. Plötz, Jan M. Wit, Philip Stanier, Gudrun E. Moore, Raoul C. M. Hennekam

    I whakaputaina 2018
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  8. 8
    Sequencing the GRHL3 Coding Region Reveals Rare Truncating Mutations and a Common Susceptibility Variant for Nonsyndromic Cleft Palate

    Sequencing the GRHL3 Coding Region Reveals Rare Truncating Mutations and a Common Susceptibility Variant for Nonsyndromic Cleft Palate mā Elisabeth Mangold, Anne C. Böhmer, Nina Ishorst, Ann‐Kathrin Hoebel, Pınar Gültepe, Hannah Schuenke, Johanna Klamt, Andrea Hofmann, Lina Gölz, Ruth Raff, Peter Teßmann, Stefanie Nowak, Heiko Reutter, Alexander Hemprich, Thomas Kreusch, Franz‐Josef Kramer, Bert Braumann, Rudolf H. Reich, Gül Schmidt, Andreas Jäger, Rudolf Reiter, Sibylle Brosch, Janis Stavusis, Miho Ishida, Rimante Seselgyte, Gudrun E. Moore, Markus M. Nöthen, Guntram Borck, Khalid Aldhorae, Baiba Lāce, Philip Stanier, Michael Knapp, Kerstin U. Ludwig

    I whakaputaina 2016
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  9. 9
    Mutations in SNX14 Cause a Distinctive Autosomal-Recessive Cerebellar Ataxia and Intellectual Disability Syndrome

    Mutations in SNX14 Cause a Distinctive Autosomal-Recessive Cerebellar Ataxia and Intellectual Disability Syndrome mā Anna Thomas, Hywel Williams, Núria Setó‐Salvia, Chiara Bacchelli, Dagan Jenkins, Mary E. O’Sullivan, Konstantinos Mengrelis, Miho Ishida, Louise Ocaka, Estelle Chanudet, Chela James, Francesco Lescai, Glenn Anderson, Deborah Morrogh, Mina Ryten, Andrew Duncan, Yun Jin Pai, Jorge Saraiva, Fabiana Ramos, Bernadette Farren, Dawn E. Saunders, Bertrand Vernay, Paul Gissen, Anna Straatmaan-Iwanowska, Frank Baas, Nicholas Wood, Joshua Hersheson, Henry Houlden, Jane A. Hurst, Richard H. Scott, Maria Bitner‐Glindzicz, Gudrun E. Moore, Sérgio B. Sousa, Philip Stanier

    I whakaputaina 2014
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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