検索結果 - Anne Seawright

  • 検索結果 1 - 9 結果 / 9
結果の絞り込み
  1. 1
    Conserved elements in Pax6 intron 7 involved in (auto)regulation and alternative transcription

    Conserved elements in Pax6 intron 7 involved in (auto)regulation and alternative transcription 著者: Dirk A. Kleinjan, Anne Seawright, Andrew J. Childs, Veronica van Heyningen

    出版事項 2003
    全文の入手
    Artigo
    お気に入りに追加
    保存先:
  2. 2
    Aniridia-associated translocations, DNase hypersensitivity, sequence comparison and transgenic analysis redefine the functional domain of PAX6

    Aniridia-associated translocations, DNase hypersensitivity, sequence comparison and transgenic analysis redefine the functional domain of PAX6 著者: Dirk A. Kleinjan, Anne Seawright, Andreas Schedl, Roy A. Quinlan, Sarah Danes, Veronica van Heyningen

    出版事項 2001
    全文の入手 全文の入手
    Artigo
    お気に入りに追加
    保存先:
  3. 3
    Role for the Wilms tumor gene in genital development?

    Role for the Wilms tumor gene in genital development? 著者: Veronica van Heyningen, Wendy A. Bickmore, Anne Seawright, Judy Fletcher, John Maule, G. Fekete, Manfred Gessler, G.A.P. Bruns, Marc Jeanpierre, Claudine Junien

    出版事項 1990
    全文の入手
    Artigo
    お気に入りに追加
    保存先:
  4. 4
    Long-range downstream enhancers are essential for Pax6 expression

    Long-range downstream enhancers are essential for Pax6 expression 著者: Dirk A. Kleinjan, Anne Seawright, Sébastien Mella, Catherine B. Carr, David A. Tyas, T. Ian Simpson, John O. Mason, David J. Price, Veronica van Heyningen

    出版事項 2006
    全文の入手
    Artigo
    お気に入りに追加
    保存先:
  5. 5
    HRAS1-selected chromosome transfer generates markers that colocalize aniridia- and genitourinary dysplasia-associated translocation breakpoints and the Wilms tumor gene within band 11p13.

    HRAS1-selected chromosome transfer generates markers that colocalize aniridia- and genitourinary dysplasia-associated translocation breakpoints and the Wilms tumor gene within band... 著者: David J. Porteous, Wendy A. Bickmore, S. Christie, Patricia A. Boyd, Gwen Cranston, Judy Fletcher, John R. Gosden, Derek Rout, Anne Seawright, K. O. J. Simola

    出版事項 1987
    全文の入手
    Artigo
    お気に入りに追加
    保存先:
  6. 6
    Molecular analysis of chromosome 11 deletions in aniridia-Wilms tumor syndrome.

    Molecular analysis of chromosome 11 deletions in aniridia-Wilms tumor syndrome. 著者: Veronica van Heyningen, Patricia A. Boyd, Anne Seawright, Judy Fletcher, Judy Fantes, K.E. Buckton, G. Spowart, David J. Porteous, Robert E. Hill, M. S. NEWTON

    出版事項 1985
    全文の入手
    Artigo
    お気に入りに追加
    保存先:
  7. 7
    Subfunctionalization of Duplicated Zebrafish pax6 Genes by cis-Regulatory Divergence

    Subfunctionalization of Duplicated Zebrafish pax6 Genes by cis-Regulatory Divergence 著者: Dirk A. Kleinjan, Ruth M Bancewicz, Philippe Gautier, Ralf Dahm, Helia B. Schönthaler, Giuseppe Damante, Anne Seawright, Ann Hever, Patricia L. Yeyati, Veronica van Heyningen, Pedro M. Coutinho

    出版事項 2008
    全文の入手 全文の入手
    Artigo
    お気に入りに追加
    保存先:
  8. 8
    A Restricted Repertoire of De Novo Mutations in ITPR1 Cause Gillespie Syndrome with Evidence for Dominant-Negative Effect

    A Restricted Repertoire of De Novo Mutations in ITPR1 Cause Gillespie Syndrome with Evidence for Dominant-Negative Effect 著者: Meriel McEntagart, Kathleen A. Williamson, Jacqueline K. Rainger, Ann P. Wheeler, Anne Seawright, Elfride De Baere, Hannah Verdin, L. Therese Bergendahl, Alan J. Quigley, Joe Rainger, Abhijit Dixit, Ajoy Sarkar, Eduardo Laso, Rocío Sánchez‐Carpintero, Jesús Barrio‐Barrio, Pierre Bitoun, Trine Prescott, Ruth Riise, Shane McKee, Jackie Cook, Lisa McKie, Berten Ceulemans, Françoise Meire, I. Karen Temple, Fabienne Prieur, Jonathan Williams, Penny Clouston, Andrea H. Németh, Siddharth Banka, Hemant Bengani, Mark T. Handley, Elisabeth Freyer, Allyson Ross, Veronica van Heyningen, Joseph A. Marsh, Frances Elmslie, David Fitzpatrick

    出版事項 2016
    全文の入手
    Artigo
    お気に入りに追加
    保存先:
  9. 9
    Monoallelic and Biallelic Mutations in MAB21L2 Cause a Spectrum of Major Eye Malformations

    Monoallelic and Biallelic Mutations in MAB21L2 Cause a Spectrum of Major Eye Malformations 著者: Joe Rainger, Davut Pehli̇van, Stefan Johansson, Hemant Bengani, Luis Sánchez‐Pulido, Kathleen A. Williamson, Mehmet Türe, Heather Barker, Karen Rosendahl, Jürgen W. Spranger, Denise Horn, Alison Meynert, James Floyd, Trine Prescott, Carl A. Anderson, Jacqueline K. Rainger, Ender Karaca, Claudia Gonzaga‐Jauregui, Shalini N. Jhangiani, Donna M. Muzny, Anne Seawright, Dinesh C. Soares, Mira Kharbanda, Victoria Murday, Andrew J. Finch, Richard A. Gibbs, Veronica van Heyningen, Martin S. Taylor, Tahsin Yakut, Per M. Knappskog, Matthew E. Hurles, Chris P. Ponting, James R. Lupski, Gunnar Houge, David Fitzpatrick, Matthew E. Hurles, David Fitzpatrick, Saeed Al-Turki, Carl A. Anderson, Inês Barroso, Philip L. Beales, Jamie Bentham, Shoumo Bhattacharya, Keren Carss, Krishna Chatterjee, Sebhattin Cirak, Catherine Cosgrove, Allan Daly, Jamie Floyd, Chris Franklin, Marta Futema, Steve E. Humphries, Shane McCarthy, Hannah M. Mitchison, Francesco Muntoni, Alexandros Onoufriadis, Victoria Parker, Felicity Payne, Vincent Plagnol, Lucy Raymond, David B. Savage, Peter Scambler, Miriam Schmidts, Robert K. Semple, Eva Serra, Jim Stalker, Margriet van Kogelenberg, Parthiban Vijayarangakannan, Klaudia Walter, G Black Wood

    出版事項 2014
    全文の入手
    Artigo
    お気に入りに追加
    保存先:

検索ツール: