Resultados da pesquisa - Miho Ishida

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  1. 1
    The role of imprinted genes in humans

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

    Publicado em 2012
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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 Por Satomi Nadanaka, Miho Ishida, Masami Ikegami, Hiroshi Kitagawa

    Publicado em 2008
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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 Por Toru Uyama, Miho Ishida, Tomomi Izumikawa, Edward Trybala, Frank Tufaro, Tomas Bergström, Kazuyuki Sugahara, Hiroshi Kitagawa

    Publicado em 2006
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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 Por 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

    Publicado em 2013
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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 Por 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

    Publicado em 2025
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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 Por 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

    Publicado em 2015
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  7. 7
    Genetic Analyses in Small-for-Gestational-Age Newborns

    Genetic Analyses in Small-for-Gestational-Age Newborns Por 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

    Publicado em 2018
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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 Por 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

    Publicado em 2016
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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 Por 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

    Publicado em 2014
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