检索结果 - Darren Fowler

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  1. 1
    Insulin-like growth factor binding protein-1 (IGFBP-1): a multifunctional role in the human female reproductive tract

    Insulin-like growth factor binding protein-1 (IGFBP-1): a multifunctional role in the human female reproductive tract 由 Darren Fowler

    出版 2000
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    Revisão
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  2. 2
    N‐methyl‐D‐aspartate receptor antibody production from germinal center reactions: Therapeutic implications

    N‐methyl‐D‐aspartate receptor antibody production from germinal center reactions: Therapeutic implications 由 Mateusz Makuch, R. Wilson, Adam Al‐Diwani, James Varley, Anne‐Kathrin Kienzler, Jennifer Taylor, Antonio Berretta, Darren Fowler, Belinda Lennox, Maria Isabel Leite, Patrick Waters, Sarosh R. Irani

    出版 2018
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    Artigo
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  3. 3
    Spatiotemporal analysis of human intestinal development at single-cell resolution

    Spatiotemporal analysis of human intestinal development at single-cell resolution 由 David Fawkner-Corbett, Agne Antanaviciute, Kaushal Parikh, Marta Jagielowicz, Ana Sousa Gerós, Tarun Gupta, Neil Ashley, Doran Khamis, Darren Fowler, Edward Morrissey, Chris Cunningham, P. V. Johnson, Hashem Koohy, Alison Simmons

    出版 2021
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    Artigo
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  4. 4
    Cervical lymph nodes and ovarian teratomas as germinal centres in NMDA receptor-antibody encephalitis

    Cervical lymph nodes and ovarian teratomas as germinal centres in NMDA receptor-antibody encephalitis 由 Adam Al‐Diwani, Jakob Theorell, Valentina Damato, Joshua A. Bull, Nicholas McGlashan, Edward Green, Anne‐Kathrin Kienzler, Ruby Harrison, Tasneem Hassanali, Leticia Campo, Molly Browne, Alistair Easton, Hooman Soleymani majd, Keiko Tenaka, Raffaele Iorio, Russell C. Dale, Paul J. Harrison, John Geddes, Digby Quested, David Sharp, Soon‐Tae Lee, David W. Nauen, Mateusz Makuch, Belinda Lennox, Darren Fowler, Fintan Sheerin, Patrick Waters, Maria Isabel Leite, Adam E. Handel, Sarosh R. Irani

    出版 2022
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    Artigo
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  5. 5
    EXOSC3 mutations in pontocerebellar hypoplasia type 1: novel mutations and genotype-phenotype correlations

    EXOSC3 mutations in pontocerebellar hypoplasia type 1: novel mutations and genotype-phenotype correlations 由 Veerle Rc Eggens, P. G. Barth, Jikke-Mien F. Niermeijer, Jonathan Berg, Niklas Darín, Abhijit Dixit, Joël Fluss, Nicola Foulds, Darren Fowler, Tibor Hortobágyi, Thomas S. Jacques, Mary D. King, Periklis Makrythanasis, Adrienn Máté, James A. R. Nicoll, Declan O’Rourke, Sue Price, Andrew N. Williams, Louise C. Wilson, Mohnish Suri, László Sztriha, Marit B Dijns-de Wissel, Mia T van Meegen, Fred van Ruissen, Eleonora Aronica, Dirk Troost, Charles B.L.M. Majoie, Henk A. Marquering, Bwee Tien Poll‐The, Frank Baas

    出版 2014
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    Artigo
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  6. 6
    The impact of inversions across 33,924 families with rare disease from a national genome sequencing project

    The impact of inversions across 33,924 families with rare disease from a national genome sequencing project 由 Alistair T. Pagnamenta, Jing Yu, Susan Walker, Alexandra Noble, Jenny Lord, Prasun Dutta, Mona Hashim, Carlos Camps, Hannah Green, Smrithi Devaiah, Lina Nashef, Jason Parr, Carl Fratter, Rana Hussein, Sarah Lindsay, Fiona Lalloo, Benito Banos‐Pinero, David M. Evans, Lucy Mallin, Adrian J. Waite, Julie Evans, Andrew G. Newman, Zoe Allen, Cristina Perez‐Becerril, Gavin Ryan, Rachel Hart, John‐Stephen Taylor, Tina Bedenham, Emma Clement, Ed Blair, Eleanor Hay, Francesca Forzano, Jenny Higgs, Natalie Canham, Anirban Majumdar, Meriel McEntagart, Nayana Lahiri, Helen Stewart, Sarah Smithson, Eduardo Calpena, Adam Jackson, Siddharth Banka, Hannah Titheradge, Ruth McGowan, Julia Rankin, Charles Shaw‐Smith, D. Gareth Evans, George J. Burghel, Miriam J. Smith, Emily E. Anderson, Rajesh Madhu, Helen V. Firth, Sian Ellard, Paul Brennan, Claire Anderson, Doug Taupin, Mark T. Rogers, Jackie A. Cook, Miranda Durkie, James E. East, Darren Fowler, Louise C. Wilson, Rebecca Igbokwe, Alice Gardham, Ian Tomlinson, Diana Baralle, Holm H. Uhlig, Jenny C. Taylor

    出版 2024
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    Artigo
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