Kết quả tìm kiếm - Joanne Morgan

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  1. 1
    Motivational deficits after brain injury: effects of bromocriptine in 11 patients.

    Motivational deficits after brain injury: effects of bromocriptine in 11 patients. Bằng Jane H. Powell, Samir Al‐Adawi, Joanne Morgan, Richard Greenwood

    Được phát hành 1996
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    Artigo
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  2. 2
    Young Offenders’ Emotion Recognition Dysfunction Across Emotion Intensities: Explaining Variation Using Psychopathic Traits, Conduct Disorder and Offense Severity

    Young Offenders’ Emotion Recognition Dysfunction Across Emotion Intensities: Explaining Variation Using Psychopathic Traits, Conduct Disorder and Offense Severity Bằng Katharine L. Bowen, Joanne Morgan, Simon Moore, Stephanie H.M. van Goozen

    Được phát hành 2013
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    Artigo
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  3. 3
    Cardiac malformations and midline skeletal defects in mice lacking filamin A

    Cardiac malformations and midline skeletal defects in mice lacking filamin A Bằng Alan Hart, Joanne Morgan, Jürgen E. Schneider, Katrine West, Lisa McKie, Shoumo Bhattacharya, Ian J. Jackson, Sally H. Cross

    Được phát hành 2006
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    Artigo
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  4. 4
    Genetic diagnosis of familial breast cancer using clonal sequencing

    Genetic diagnosis of familial breast cancer using clonal sequencing Bằng Joanne Morgan, Ian Carr, Eamonn Sheridan, Carol Chu, Bruce E. Hayward, Nick Camm, Helen Lindsay, Chris Mattocks, Alexander F. Markham, David T. Bonthron, Graham R. Taylor

    Được phát hành 2010
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    Artigo
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  5. 5
    Next-Generation Sequencing for Simultaneous Determination of Human Papillomavirus Load, Subtype, and Associated Genomic Copy Number Changes in Tumors

    Next-Generation Sequencing for Simultaneous Determination of Human Papillomavirus Load, Subtype, and Associated Genomic Copy Number Changes in Tumors Bằng Caroline Conway, Rebecca Chalkley, A.S. High, Kenneth MacLennan, Stefano Berri, Preetha Chengot, Melissa Alsop, Philip Egan, Joanne Morgan, Graham R. Taylor, John Chester, Mehmet Şen, Pamela Rabbitts, Henry M. Wood

    Được phát hành 2012
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    Artigo
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  6. 6
    Novel ENU-induced eye mutations in the mouse: models for human eye disease

    Novel ENU-induced eye mutations in the mouse: models for human eye disease Bằng Caroline Thaung, Katrine West, Brian J. Clark, Lisa McKie, Joanne Morgan, Karen South Arnold, Patrick M. Nolan, Jo Peters, A. Jackie Hunter, Steve D. M. Brown, Ian J. Jackson, Sally H. Cross

    Được phát hành 2002
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    Artigo
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  7. 7
    Simple and Efficient Identification of Rare Recessive Pathologically Important Sequence Variants from Next Generation Exome Sequence Data

    Simple and Efficient Identification of Rare Recessive Pathologically Important Sequence Variants from Next Generation Exome Sequence Data Bằng Ian Carr, Joanne Morgan, Christopher M. Watson, Svitlana Melnik, Christine P. Diggle, Clare V. Logan, Sally M. Harrison, Graham R. Taylor, Sérgio D.J. Pena, Alexander F. Markham, Fowzan S. Alkuraya, Graeme Black, Manir Ali, David T. Bonthron

    Được phát hành 2013
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    Artigo
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  8. 8
    Complement C3 Variant and the Risk of Age-Related Macular Degeneration

    Complement C3 Variant and the Risk of Age-Related Macular Degeneration Bằng John R.W. Yates, Tiina Sepp, Baljinder K. Matharu, Jane C. Khan, Deborah A. Thurlby, Humma Shahid, David Clayton, Caroline Hayward, Joanne Morgan, Alan F. Wright, Ana Maria Armbrecht, Baljean Dhillon, Ian J. Deary, Elizabeth Redmond, Alan C. Bird, Anthony T. Moore

    Được phát hành 2007
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    Artigo
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  9. 9
    Expression quantitative trait loci in the developing human brain and their enrichment in neuropsychiatric disorders

    Expression quantitative trait loci in the developing human brain and their enrichment in neuropsychiatric disorders Bằng Heath O’Brien, Eilís Hannon, Matthew Hill, Carolina Toste, Matthew J. Robertson, Joanne Morgan, Gemma M. McLaughlin, Cathryn M. Lewis, Leonard C. Schalkwyk, Lynsey S. Hall, Antonio F. Pardiñas, Michael J. Owen, Michael O’Donovan, Jonathan Mill, Nicholas J. Bray

    Được phát hành 2018
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    Artigo
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  10. 10
    Peer-led walking programme to increase physical activity in inactive 60- to 70-year-olds: Walk with Me pilot RCT

    Peer-led walking programme to increase physical activity in inactive 60- to 70-year-olds: Walk with Me pilot RCT Bằng Mark A. Tully, Conor Cunningham, Ashlene Wright, Ilona McMullan, Julie Doherty, Debbie Collins, Catrine Tudor‐Locke, Joanne Morgan, Glenn Phair, Bob Laventure, E. Simpson, Suzanne McDonough, Evie Gardner, Frank Kee, Marie Murphy, Ashley Agus, Ruth F. Hunter, Wendy Hardeman, Margaret Cupples

    Được phát hành 2019
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    Artigo
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  11. 11
    Using next-generation sequencing for high resolution multiplex analysis of copy number variation from nanogram quantities of DNA from formalin-fixed paraffin-embedded specimens

    Using next-generation sequencing for high resolution multiplex analysis of copy number variation from nanogram quantities of DNA from formalin-fixed paraffin-embedded specimens Bằng Henry M. Wood, Ornella Belvedere, Caroline Conway, Catherine Daly, Rebecca Chalkley, Melissa Bickerdike, Claire McKinley, Phil Egan, Lisa Ross, Bruce E. Hayward, Joanne Morgan, Leslie Davidson, Ken MacLennan, Thian K. Ong, Kostas Papagiannopoulos, Ian A. Cook, David J. Adams, Graham R. Taylor, Pamela Rabbitts

    Được phát hành 2010
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    Artigo
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  12. 12
    Next generation sequencing identifies mutations in Atonal homolog 7 (ATOH7) in families with global eye developmental defects

    Next generation sequencing identifies mutations in Atonal homolog 7 (ATOH7) in families with global eye developmental defects Bằng Kamron Khan, Clare V. Logan, Martin McKibbin, Eamonn Sheridan, Nursel Elçioğlu, Özlem Yenice, David Parry, Narcís Fernández‐Fuentes, Zakia Abdelhamed, Ahmed Al-Maskari, James A. Poulter, Moin Mohamed, Ian Carr, Joanne Morgan, Hussain Jafri, Yasmin Raashid, Graham R. Taylor, Colin A. Johnson, Chris F. Inglehearn, Carmel Toomes, Manir Ali

    Được phát hành 2011
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    Artigo
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  13. 13
    Mutations in C4orf26, Encoding a Peptide with In Vitro Hydroxyapatite Crystal Nucleation and Growth Activity, Cause Amelogenesis Imperfecta

    Mutations in C4orf26, Encoding a Peptide with In Vitro Hydroxyapatite Crystal Nucleation and Growth Activity, Cause Amelogenesis Imperfecta Bằng David Parry, Steven J. Brookes, Clare V. Logan, James A. Poulter, Walid El‐Sayed, Suhaila Al‐Bahlani, Sharifa Al-Harasi, Jihad Sayed, El Mostafa Raïf, Richard F. Shore, Mayssoon Dashash, Martin Barron, Joanne Morgan, Ian Carr, Graham R. Taylor, Colin A. Johnson, Michael J. Aldred, Michael J. Dixon, J. Tim Wright, Jennifer Kirkham, Chris F. Inglehearn, Alan J. Mighell

    Được phát hành 2012
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    Artigo
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  14. 14
    De novo mutations identified by exome sequencing implicate rare missense variants in SLC6A1 in schizophrenia

    De novo mutations identified by exome sequencing implicate rare missense variants in SLC6A1 in schizophrenia Bằng Elliott Rees, Jun Han, Joanne Morgan, Noa Carrera, Valentina Escott‐Price, Andrew Pocklington, Madeleine Duffield, Lynsey S. Hall, Sophie E. Legge, Antonio F. Pardiñas, Alexander Richards, Julian Roth, Tatyana Lezheiko, Nikolay Kondratyev, Василий Глебович Каледа, В. Е. Голимбет, Mara Parellada, Javier González‐Peñas, Celso Arango, Micha Gawlik, George Kirov, James Walters, Peter Holmans, Michael O’Donovan, Michael J. Owen

    Được phát hành 2020
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    Artigo
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  15. 15
    Homozygous Mutations in PXDN Cause Congenital Cataract, Corneal Opacity, and Developmental Glaucoma

    Homozygous Mutations in PXDN Cause Congenital Cataract, Corneal Opacity, and Developmental Glaucoma Bằng Kamron Khan, Adam K Rudkin, David Parry, Kathryn P. Burdon, Martin McKibbin, Clare V. Logan, Zakia Abdelhamed, James Muecke, Narcís Fernández‐Fuentes, Kate J. Laurie, Mike Shires, Rhys A Fogarty, Ian Carr, James A. Poulter, Joanne Morgan, Moin Mohamed, Hussain Jafri, Yasmin Raashid, Ngy Meng, Horm Piseth, Carmel Toomes, Robert J. Casson, Graham R. Taylor, Michael Hammerton, Eamonn Sheridan, Colin A. Johnson, Chris F. Inglehearn, Jamie E. Craig, Manir Ali

    Được phát hành 2011
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    Artigo
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  16. 16
    Loss-of-function mutations in MICU1 cause a brain and muscle disorder linked to primary alterations in mitochondrial calcium signaling

    Loss-of-function mutations in MICU1 cause a brain and muscle disorder linked to primary alterations in mitochondrial calcium signaling Bằng Clare V. Logan, György Szabadkai, Jenny A. Sharpe, David Parry, Silvia Torelli, Anne‐Marie Childs, Marjolein Kriek, Rahul Phadke, Colin A. Johnson, Nicola Roberts, David T. Bonthron, Karen Pysden, Tamieka Whyte, Iulia Munteanu, A. Reghan Foley, Gabrielle Wheway, Katarzyna Szymańska, Subaashini Natarajan, Zakia A. Abdelhamed, Joanne Morgan, H. Roper, Gijs W.E. Santen, Erik H. Niks, W. Ludo van der Pol, Dick Lindhout, Anna Raffaello, Diego De Stefani, Johan T. den Dunnen, Yu Sun, Ieke B. Ginjaar, Caroline A. Sewry, Matthew E. Hurles, Rosario Rizzuto, Michael R. Duchen, Francesco Muntoni, Eamonn Sheridan

    Được phát hành 2013
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    Artigo
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  17. 17
    Targeted Sequencing of 10,198 Samples Confirms Abnormalities in Neuronal Activity and Implicates Voltage-Gated Sodium Channels in Schizophrenia Pathogenesis

    Targeted Sequencing of 10,198 Samples Confirms Abnormalities in Neuronal Activity and Implicates Voltage-Gated Sodium Channels in Schizophrenia Pathogenesis Bằng Elliott Rees, Noa Carrera, Joanne Morgan, Kirsty Hambridge, Valentina Escott‐Price, Andrew Pocklington, Alexander Richards, Antonio F. Pardiñas, Colm McDonald, Gary Donohoe, Derek W. Morris, Elaine Kenny, Eric Kelleher, Michael Gill, Aiden Corvin, George Kirov, James Walters, Peter Holmans, Michael J. Owen, Michael O’Donovan, Behrooz Z. Alizadeh, Thérèse van Amelsvoort, Agna A. Bartels‐Velthuis, Nico J. van Beveren, Richard Bruggeman, Wiepke Cahn, Lieuwe de Haan, Philippe Delespaul, Carin J. Meijer, Inez Myin‐Germeys, René S. Kahn, Frederike Schirmbeck, Claudia J.P. Simons, Neeltje E.M. van Haren, Jim van Os, Ruud van Winkel, Jurjen J. Luykx

    Được phát hành 2018
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    Artigo
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