Výsledky vyhledávání - Andrew J. Rimmer

  • Zobrazuji výsledky 1 - 9 z 9
Upřesnit hledání
  1. 1
    Whole-Exome Sequencing Studies of Nonfunctioning Pituitary Adenomas

    Whole-Exome Sequencing Studies of Nonfunctioning Pituitary Adenomas Autor Paul Newey, M. Andrew Nesbit, Andrew J. Rimmer, Rosie Head, Caroline M. Gorvin, Moustafa Attar, Lorna Gregory, John Wass, David Buck, Niki Karavitaki, Ashley Grossman, Gil McVean, Olaf Ansorge, Rajesh V. Thakker

    Vydáno 2013
    Získat plný text Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  2. 2
    Whole-Exome Sequencing Studies of Nonhereditary (Sporadic) Parathyroid Adenomas

    Whole-Exome Sequencing Studies of Nonhereditary (Sporadic) Parathyroid Adenomas Autor Paul Newey, M. Andrew Nesbit, Andrew J. Rimmer, Moustafa Attar, R. A. Head, Paul T. Christie, Caroline M. Gorvin, Michael Stechman, Lorna Gregory, Radu Mihai, Greg Sadler, Gil McVean, David Buck, Rajesh V. Thakker

    Vydáno 2012
    Získat plný text Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  3. 3
    Mutations in AP2S1 cause familial hypocalciuric hypercalcemia type 3

    Mutations in AP2S1 cause familial hypocalciuric hypercalcemia type 3 Autor M. Andrew Nesbit, Fadil Hannan, Sarah Howles, Adam J. Reed, Treena Cranston, Clare Thakker, Lorna Gregory, Andrew J. Rimmer, Nigel Rust, Una Graham, Patrick J. Morrison, Steven Hunter, Michael P. Whyte, Gil McVean, David Buck, Rajesh V. Thakker

    Vydáno 2012
    Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  4. 4
    Unlocking the Bottleneck in Forward Genetics Using Whole-Genome Sequencing and Identity by Descent to Isolate Causative Mutations

    Unlocking the Bottleneck in Forward Genetics Using Whole-Genome Sequencing and Identity by Descent to Isolate Causative Mutations Autor Katherine R. Bull, Andrew J. Rimmer, Owen M. Siggs, Lisa A. Miosge, Carla M. Roots, Anselm Enders, Edward M. Bertram, Tanya L. Crockford, Belinda Whittle, Paul Potter, Michelle M. Simon, Ann‐Marie Mallon, Steve D. M. Brown, Bruce Beutler, Christopher C. Goodnow, Gerton Lunter, Richard J. Cornall

    Vydáno 2013
    Získat plný text Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  5. 5
    B cell survival, surface BCR and BAFFR expression, CD74 metabolism, and CD8− dendritic cells require the intramembrane endopeptidase SPPL2A

    B cell survival, surface BCR and BAFFR expression, CD74 metabolism, and CD8− dendritic cells require the intramembrane endopeptidase SPPL2A Autor H Bergmann, Mehmet Yabas, Alanna Short, Lisa A. Miosge, Nadine Barthel, Charis E. Teh, Carla M. Roots, Katherine R. Bull, Yogesh Jeelall, Keisuke Horikawa, Belinda Whittle, Bhavani Balakishnan, Geoff Sjollema, Edward M. Bertram, Fabienne Mackay, Andrew J. Rimmer, Richard J. Cornall, Matthew A. Field, T. Daniel Andrews, Christopher C. Goodnow, Anselm Enders

    Vydáno 2012
    Získat plný text Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  6. 6
    Evolutionary dynamics of <i>Staphylococcus aureus</i> during progression from carriage to disease

    Evolutionary dynamics of <i>Staphylococcus aureus</i> during progression from carriage to disease Autor Bernadette C. Young, Tanya Golubchik, Elizabeth M. Batty, Rowena Fung, Hanna Larner-Svensson, Antonina A. Votintseva, Ruth R. Miller, Heather Godwin, Kyle Knox, Richard G. Everitt, Zamin Iqbal, Andrew J. Rimmer, Madeleine Cule, Camilla L. C. Ip, Xavier Didelot, Rosalind M. Harding, Peter Donnelly, Tim Peto, Derrick W. Crook, Rory Bowden, Daniel J. Wilson

    Vydáno 2012
    Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  7. 7
    A point mutation in the ion conduction pore of AMPA receptor GRIA3 causes dramatically perturbed sleep patterns as well as intellectual disability

    A point mutation in the ion conduction pore of AMPA receptor GRIA3 causes dramatically perturbed sleep patterns as well as intellectual disability Autor Benjamin Davies, Laurence A. Brown, Ondřej Cais, Jake F. Watson, Amber J. Clayton, Veronica T. Chang, Daniel Biggs, Christopher Preece, Polinka Hernandez-Pliego, Jon P. Krohn, Amarjit Bhomra, Stephen R.F. Twigg, Andrew J. Rimmer, Alexander Kanapin, Arjune Sen, Zenobia Zaiwalla, Gil McVean, F. Foster, Peter Donnelly, Jenny C. Taylor, Edward Blair, David Nutt, A.R. Aricescu, Ingo H. Greger, Stuart N. Peirson, Jonathan Flint, Hilary C. Martin

    Vydáno 2017
    Získat plný text Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  8. 8
    Recessive Mutations in SPTBN2 Implicate β-III Spectrin in Both Cognitive and Motor Development

    Recessive Mutations in SPTBN2 Implicate β-III Spectrin in Both Cognitive and Motor Development Autor Stefano Lise, Yvonne L. Clarkson, Emma Perkins, Alexandra Kwasniewska, Elham Sadighi Akha, Ricardo Parolin Schnekenberg, Daumante Šuminaite, Jilly Hope, Ian Baker, Lorna Gregory, Angie Green, Chris Allan, Sarah Lamble, Sandeep Jayawant, Gerardine Quaghebeur, M. Zameel Cader, Sarah Hughes, Richard Armstrong, Alexander Kanapin, Andrew J. Rimmer, Gerton Lunter, Iain Mathieson, Jean‐Baptiste Cazier, David Buck, Jenny C. Taylor, David Bentley, Gil McVean, Peter Donnelly, Samantha J.L. Knight, M. T. Jackson, Jiannis Ragoussis, Andrea H. Németh

    Vydáno 2012
    Získat plný text Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  9. 9
    Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancer

    Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancer Autor Elise Ruark, Katie Snape, Peter Humburg, Chey Loveday, Ilirjana Bajrami, Rachel Brough, Daniel Nava Rodrigues, Anthony Renwick, Sheila Seal, Emma Ramsay, Silvana Del Vecchio Duarte, Manuel A. Rivas, Margaret Warren-Perry, Anna Zachariou, Adriana Campion‐Flora, Sandra Hanks, Anne R. Murray, Naser Ansari‐Pour, Jenny Douglas, Lorna Gregory, Andrew J. Rimmer, Neil Walker, Tsun-Po Yang, Julian Adlard, Julian Barwell, Jonathan Berg, Angela F. Brady, Carole Brewer, Glen Brice, Cyril Chapman, Jackie Cook, Rosemarie Davidson, Alan Donaldson, Fiona Douglas, Diana Eccles, D. Gareth Evans, Lynn Greenhalgh, Alex Henderson, Louise Izatt, Ajith Kumar, Fiona Lalloo, Zosia Miedzybrodzka, Patrick J. Morrison, Joan Paterson, Mary Porteous, Mark T. Rogers, Susan Shanley, Lisa Walker, Martin Gore, Richard S. Houlston, Matthew A. Brown, Mark J. Caufield, Panos Deloukas, Mark I. McCarthy, John A. Todd, Clare Turnbull, Jorge S. Reis‐Filho, Alan Ashworth, Antonis C. Antoniou, Christopher J. Lord, Peter Donnelly, Nazneen Rahman

    Vydáno 2012
    Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:

Vyhledávací nástroje: