Výsledky vyhledávání - Kathryn Robson
- Zobrazuji výsledky 1 - 16 z 16
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The A-domain and the thrombospondin-related motif of Plasmodium falciparum TRAP are implicated in the invasion process of mosquito salivary glands Autor Kai Wengelnik, Roberta Spaccapelo, Silvia Naitza, Kathryn Robson, Chris J. Janse, Francesco Bistoni, Andrew P. Waters, Andrea Crisanti
Vydáno 1999Artigo -
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A valine deletion of ferroportin 1: a common mutation in hemochromatosis type 4? Autor Antonella Roetto, Alison T. Merryweather‐Clarke, Filomena Daraio, Karen Livesey, Jennifer J. Pointon, Giuliana Barbabietola, Antonio Piga, P H Mackie, Kathryn Robson, Clara Camaschella
Vydáno 2002Carta -
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In vitro functional analysis of human ferroportin (FPN) and hemochromatosis-associated FPN mutations Autor 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
Vydáno 2005Artigo -
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Resistance to hepcidin is conferred by hemochromatosis-associated mutations of ferroportin Autor 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
Vydáno 2005Artigo -
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A Neolithic expansion, but strong genetic structure, in the independent history of New Guinea Autor 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
Vydáno 2017Artigo -
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Multicentric Origin of Hemochromatosis Gene (HFE) Mutations Autor 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
Vydáno 1999Artigo -
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Global gene expression analysis of human erythroid progenitors Autor 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
Vydáno 2011Artigo -
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Mutations in the β-Tubulin Gene TUBB5 Cause Microcephaly with Structural Brain Abnormalities Autor 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
Vydáno 2012Artigo -
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Association between a common immunoglobulin heavy chain allele and rheumatic heart disease risk in Oceania Autor 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
Vydáno 2017Artigo -
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A loss-of-function <i>IFNAR1</i> allele in Polynesia underlies severe viral diseases in homozygotes Autor 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
Vydáno 2022Artigo -
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Factors influencing success of clinical genome sequencing across a broad spectrum of disorders Autor 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
Vydáno 2015Artigo
Vyhledávací nástroje:
Související témata
Biology
Gene
Genetics
Mutation
Allele
Cell biology
Hemochromatosis
Immunology
Medicine
Molecular biology
Amino acid
Biochemistry
Complementary DNA
Ferroportin
Haplotype
Hepcidin
Hereditary hemochromatosis
Internal medicine
Anemia
Chemistry
Computational biology
Evolutionary biology
Ferritin
Founder effect
Genome
Genotype
Gliding motility
Inflammation
Malaria
Missense mutation