Torthaí cuardaigh - Kathryn Robson

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  1. 1
    Global prevalence of putative haemochromatosis mutations.

    Global prevalence of putative haemochromatosis mutations. de réir Alison T. Merryweather‐Clarke, J. J. Pointon, Jeremy D. Shearman, Kathryn Robson

    Foilsithe / Cruthaithe 1997
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  2. 2
    Polysome immunoprecipitation of phenylalanine hydroxylase mRNA from rat liver and cloning of its cDNA.

    Polysome immunoprecipitation of phenylalanine hydroxylase mRNA from rat liver and cloning of its cDNA. de réir Kathryn Robson, T.S. Chandra, Ross T. A. MacGillivray, Savio L.C. Woo

    Foilsithe / Cruthaithe 1982
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  3. 3
    Construction and identification of mouse amelogenin cDNA clones.

    Construction and identification of mouse amelogenin cDNA clones. de réir ML Snead, M Zeichner‐David, T.S. Chandra, Kathryn Robson, S L Woo, H.C. Slavkin

    Foilsithe / Cruthaithe 1983
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  4. 4
    TRAP Is Necessary for Gliding Motility and Infectivity of Plasmodium Sporozoites

    TRAP Is Necessary for Gliding Motility and Infectivity of Plasmodium Sporozoites de réir Ali A. Sultan, Vandana Thathy, Ute Frevert, Kathryn Robson, Andrea Crisanti, Victor Nussenzweig, Ruth S. Nussenzweig, Robert Ménard

    Foilsithe / Cruthaithe 1997
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  5. 5
    GT to AT transition at a splice donor site causes skipping of the preceding exon in Phenylketonuria

    GT to AT transition at a splice donor site causes skipping of the preceding exon in Phenylketonuria de réir Joshua Marvit, Anthony G. DiLella, Kelly A. Brayton, Fred D. Ledley, Kathryn Robson, S.L.C. Woo

    Foilsithe / Cruthaithe 1987
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  6. 6
    The A-domain and the thrombospondin-related motif of Plasmodium falciparum TRAP are implicated in the invasion process of mosquito salivary glands

    The A-domain and the thrombospondin-related motif of Plasmodium falciparum TRAP are implicated in the invasion process of mosquito salivary glands de réir Kai Wengelnik, Roberta Spaccapelo, Silvia Naitza, Kathryn Robson, Chris J. Janse, Francesco Bistoni, Andrew P. Waters, Andrea Crisanti

    Foilsithe / Cruthaithe 1999
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  7. 7
    A valine deletion of ferroportin 1: a common mutation in hemochromatosis type 4?

    A valine deletion of ferroportin 1: a common mutation in hemochromatosis type 4? de réir Antonella Roetto, Alison T. Merryweather‐Clarke, Filomena Daraio, Karen Livesey, Jennifer J. Pointon, Giuliana Barbabietola, Antonio Piga, P H Mackie, Kathryn Robson, Clara Camaschella

    Foilsithe / Cruthaithe 2002
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  8. 8
    In vitro functional analysis of human ferroportin (FPN) and hemochromatosis-associated FPN mutations

    In vitro functional analysis of human ferroportin (FPN) and hemochromatosis-associated FPN mutations de réir Lisa Schimanski, Hal Drakesmith, Alison T. Merryweather‐Clarke, Vip Viprakasit, Jon P. Edwards, Emma Sweetland, Judy Bastin, Diana Cowley, Yingyong Chinthammitr, Kathryn Robson, Alain Townsend

    Foilsithe / Cruthaithe 2005
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  9. 9
    Resistance to hepcidin is conferred by hemochromatosis-associated mutations of ferroportin

    Resistance to hepcidin is conferred by hemochromatosis-associated mutations of ferroportin de réir Hal Drakesmith, Lisa Schimanski, Emma Ormerod, Alison T. Merryweather‐Clarke, Vip Viprakasit, Jon P. Edwards, Emma Sweetland, Judy Bastin, Diana Cowley, Yingyong Chinthammitr, Kathryn Robson, Alain Townsend

    Foilsithe / Cruthaithe 2005
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  10. 10
    A Neolithic expansion, but strong genetic structure, in the independent history of New Guinea

    A Neolithic expansion, but strong genetic structure, in the independent history of New Guinea de réir Anders Bergström, Stephen Oppenheimer, Alexander J. Mentzer, Kathryn Auckland, Kathryn Robson, Robert Attenborough, Michael P. Alpers, George Koki, William Pomat, Peter Siba, Yali Xue, Manjinder S. Sandhu, Chris Tyler‐Smith

    Foilsithe / Cruthaithe 2017
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  11. 11
    Multicentric Origin of Hemochromatosis Gene (HFE) Mutations

    Multicentric Origin of Hemochromatosis Gene (HFE) Mutations de réir Jacques Rochette, J. J. Pointon, Christopher A. Fisher, Giathra Perera, Mahinda Arambepola, D. S. Kodikara Arichchi, S. De Silva, J.L. Vandwalle, Jean‐Pierre Monti, Julie M. Old, Alison T. Merryweather‐Clarke, D. J. Weatherall, Kathryn Robson

    Foilsithe / Cruthaithe 1999
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  12. 12
    Global gene expression analysis of human erythroid progenitors

    Global gene expression analysis of human erythroid progenitors de réir Alison T. Merryweather‐Clarke, Ann Atzberger, Shamit Soneji, Nicki Gray, Kevin Clark, Craig Waugh, Simon J. McGowan, Stephen Taylor, Asoke K. Nandi, W. G. Wood, David J. Roberts, Douglas R. Higgs, Veronica J. Buckle, Kathryn Robson

    Foilsithe / Cruthaithe 2011
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  13. 13
    Mutations in the β-Tubulin Gene TUBB5 Cause Microcephaly with Structural Brain Abnormalities

    Mutations in the β-Tubulin Gene TUBB5 Cause Microcephaly with Structural Brain Abnormalities de réir Martin W. Breuss, Julian Ik‐Tsen Heng, Karine Poirier, Guoling Tian, Xavier H. Jaglin, Zhengdong Qu, Andreas Braun, Thomas Gstrein, Linh Ngo, Matilda Haas, Nadia Bahi‐Buisson, Marie‐Laure Moutard, Sandrine Passemard, Alain Verloès, Pierre Gressèns, Yunli Xie, Kathryn Robson, Deepa Selvi Rani, Kumarasamy Thangaraj, Tim Clausen, Jamel Chelly, Nicholas J. Cowan, David A. Keays

    Foilsithe / Cruthaithe 2012
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  14. 14
    Association between a common immunoglobulin heavy chain allele and rheumatic heart disease risk in Oceania

    Association between a common immunoglobulin heavy chain allele and rheumatic heart disease risk in Oceania de réir Tom Parks, Mariana Mirabel, Joseph Kado, Kathryn Auckland, Jarosław Nowak, Anna Rautanen, Alexander J. Mentzer, Éloi Marijon, Xavier Jouven, Mai Ling Perman, Tuliana Cua, John Kauwe, John Allen, Henry M. Taylor, Kathryn Robson, Charlotte M. Deane, Andrew C. Steer, Adrian V. S. Hill, Lori Allen, M. David Allen, Corinne Braunstein, Samantha Colquhoun, Aurélia Jewine, Maureen Ah Kee, R. Uday Kumar, Martin Wj, Reapi L. Mataika, Marie Nadra, Shahin Nadu, Take Naseri, Baptiste Noël, Nathalie Simon, Brenton Ward

    Foilsithe / Cruthaithe 2017
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  15. 15
    A loss-of-function <i>IFNAR1</i> allele in Polynesia underlies severe viral diseases in homozygotes

    A loss-of-function <i>IFNAR1</i> allele in Polynesia underlies severe viral diseases in homozygotes de réir Paul Bastard, Kuang‐Chih Hsiao, Qian Zhang, Jérémy Choin, Emma Best, Jie Chen, Adrian Gervais, Lucy Bizien, Marie Materna, Christine Harmant, Maguelonne Roux, Nicola L. Hawley, Daniel E. Weeks, Stephen T. McGarvey, Karla Sandoval, Carmina Barberena-Jonas, Consuelo D. Quinto-Cortés, Erika Hagelberg, Alexander J. Mentzer, Kathryn Robson, Boubacar Coulibaly, Yoann Seeleuthner, Benedetta Bigio, Zhi Li, Gilles Uzé, Sandra Pellegrini, Lazaro Lorenzo, Zineb Sbihi, Sylvain Latour, Marianne Besnard, Tiphaine Adam de Beaumais, Evelyne Jacqz‐Aigrain, Vivien Béziat, Ranjan Deka, Litara Esera Tulifau, Satupaitea Viali, Muagututi‘a Sefuiva Reupena, Take Naseri, Peter McNaughton, Vanessa Sarkozy, Jane Peake, Annaliesse Blincoe, Sarah Primhak, Simon Stables, Kate Gibson, See‐Tarn Woon, Kylie M. Drake, Adrian V. S. Hill, Cheng-Yee Chan, Richard King, Rohan Ameratunga, Iotefa Teiti, Maïté Aubry, Van‐Mai Cao‐Lormeau, Stuart G. Tangye, Shen‐Ying Zhang, Emmanuelle Jouanguy, Paul Gray, Laurent Abel, Andrés Moreno‐Estrada, Ryan L. Minster, Lluı́s Quintana-Murci, Andrew Wood, Jean‐Laurent Casanova

    Foilsithe / Cruthaithe 2022
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  16. 16
    Factors influencing success of clinical genome sequencing across a broad spectrum of disorders

    Factors influencing success of clinical genome sequencing across a broad spectrum of disorders de réir Jenny C. Taylor, Hilary C. Martin, Stefano Lise, John Broxholme, Jean‐Baptiste Cazier, Andy Rimmer, Alexander Kanapin, Gerton Lunter, Simon Fiddy, Chris Allan, A.R. Aricescu, Moustafa Attar, Christian Babbs, Jennifer Becq, David Beeson, Celeste Bento, P Bignell, Edward Blair, Veronica J. Buckle, Katherine R. Bull, Ondřej Cais, Holger Cario, Helen Chapel, Richard R. Copley, Richard J. Cornall, Jude Craft, Karin Dahan, Emma E. Davenport, Calliope A. Dendrou, Olivier Devuyst, Aimée L Fenwick, Jonathan Flint, Lars Fugger, Rodney D. Gilbert, Anne Goriely, Angie Green, Ingo H. Greger, Russell Grocock, Anja V. Gruszczyk, Robert Hastings, Edouard Hatton, Douglas R. Higgs, Adrian V. S. Hill, Chris Holmes, Malcolm F. Howard, Linda Hughes, Peter Humburg, David H. Johnson, Fredrik Karpe, Zoya Kingsbury, Usha Kini, Julian C. Knight, Jonathan Krohn, Sarah Lamble, Craig B. Langman, Lorne Lonie, Joshua Luck, Davis J. McCarthy, Simon J. McGowan, Mary Frances McMullin, Kerry A. Miller, Lisa Murray, Andrea H. Németh, M. Andrew Nesbit, David Nutt, Elizabeth Ormondroyd, Annette Oturai, Alistair T. Pagnamenta, Smita Y. Patel, Melanie J. Percy, Nayia Petousi, Paolo Piazza, Siân E. Piret, Guadalupe Polanco‐Echeverry, Niko Popitsch, Fiona Powrie, Christopher W. Pugh, Lynn Quek, Peter A. Robbins, Kathryn Robson, Alexandra Russo, Natasha Sahgal, Pauline A. van Schouwenburg, Anna Schuh, Earl D. Silverman, Alison Simmons, Per Soelberg Sørensen, Elizabeth Sweeney, John Taylor, Rajesh V. Thakker, Ian Tomlinson, Amy Trebes, Stephen R.F. Twigg, Holm H. Uhlig, Paresh Vyas, Tim J. Vyse, Steven A. Wall, Hugh Watkins, Michael P. Whyte, Lorna Witty

    Foilsithe / Cruthaithe 2015
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