Hasil Pencarian - Ian M Smyth

  • Menampilkan 1 - 9 hasil dari 9
Perbaiki Hasil
  1. 1
    Hox10 genes function in kidney development in the differentiation and integration of the cortical stroma.

    Hox10 genes function in kidney development in the differentiation and integration of the cortical stroma. oleh Alisha R Yallowitz, Steven M Hrycaj, Kieran M Short, Ian M Smyth, Deneen M Wellik

    Diterbitkan 2011-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  2. 2
    FGF10 and the Mystery of Duodenal Atresia in Humans

    FGF10 and the Mystery of Duodenal Atresia in Humans oleh Warwick J. Teague, Warwick J. Teague, Warwick J. Teague, Warwick J. Teague, Matthew L. M. Jones, Matthew L. M. Jones, Matthew L. M. Jones, Leanne Hawkey, Ian M. Smyth, Ian M. Smyth, Ian M. Smyth, Angelique Catubig, Sebastian K. King, Sebastian K. King, Sebastian K. King, Sebastian K. King, Gulcan Sarila, Ruili Li, John M. Hutson, John M. Hutson, John M. Hutson

    Diterbitkan 2018-11-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  3. 3
    Keratin 76 is required for tight junction function and maintenance of the skin barrier.

    Keratin 76 is required for tight junction function and maintenance of the skin barrier. oleh Tia DiTommaso, Denny L Cottle, Helen B Pearson, Holger Schlüter, Pritinder Kaur, Patrick O Humbert, Ian M Smyth

    Diterbitkan 2014-10-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  4. 4
    Branching morphogenesis in the developing kidney is not impacted by nephron formation or integration

    Branching morphogenesis in the developing kidney is not impacted by nephron formation or integration oleh Kieran M Short, Alexander N Combes, Valerie Lisnyak, James G Lefevre, Lynelle K Jones, Melissa H Little, Nicholas A Hamilton, Ian M Smyth

    Diterbitkan 2018-07-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  5. 5
    Altered ureteric branching morphogenesis and nephron endowment in offspring of diabetic and insulin-treated pregnancy.

    Altered ureteric branching morphogenesis and nephron endowment in offspring of diabetic and insulin-treated pregnancy. oleh Stacey N Hokke, James A Armitage, Victor G Puelles, Kieran M Short, Lynelle Jones, Ian M Smyth, John F Bertram, Luise A Cullen-McEwen

    Diterbitkan 2013-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  6. 6
    Deletion of Aurora kinase A prevents the development of polycystic kidney disease in mice

    Deletion of Aurora kinase A prevents the development of polycystic kidney disease in mice oleh Ming Shen Tham, Denny L. Cottle, Allara K. Zylberberg, Kieran M. Short, Lynelle K. Jones, Perkin Chan, Sarah E. Conduit, Jennifer M. Dyson, Christina A. Mitchell, Ian M. Smyth

    Diterbitkan 2024-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  7. 7
    Identification of genes important for cutaneous function revealed by a large scale reverse genetic screen in the mouse.

    Identification of genes important for cutaneous function revealed by a large scale reverse genetic screen in the mouse. oleh Tia DiTommaso, Lynelle K Jones, Denny L Cottle, WTSI Mouse Genetics Program, Anna-Karin Gerdin, Valerie E Vancollie, Fiona M Watt, Ramiro Ramirez-Solis, Allan Bradley, Karen P Steel, John P Sundberg, Jacqueline K White, Ian M Smyth

    Diterbitkan 2014-10-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  8. 8
    Subtle Changes in the Levels of BCL-2 Proteins Cause Severe Craniofacial Abnormalities

    Subtle Changes in the Levels of BCL-2 Proteins Cause Severe Craniofacial Abnormalities oleh Stephanie Grabow, Andrew J. Kueh, Francine Ke, Hannah K. Vanyai, Bilal N. Sheikh, Michael A. Dengler, William Chiang, Samantha Eccles, Ian M. Smyth, Lynelle K. Jones, Frederic J. de Sauvage, Mark Scott, Lachlan Whitehead, Anne K. Voss, Andreas Strasser

    Diterbitkan 2018-09-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  9. 9
    Genome-wide ENU mutagenesis in combination with high density SNP analysis and exome sequencing provides rapid identification of novel mouse models of developmental disease.

    Genome-wide ENU mutagenesis in combination with high density SNP analysis and exome sequencing provides rapid identification of novel mouse models of developmental disease. oleh Georgina Caruana, Peter G Farlie, Adam H Hart, Stefan Bagheri-Fam, Megan J Wallace, Michael S Dobbie, Christopher T Gordon, Kerry A Miller, Belinda Whittle, Helen E Abud, Ruth M Arkell, Timothy J Cole, Vincent R Harley, Ian M Smyth, John F Bertram

    Diterbitkan 2013-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:

Alat Pencarian: