Resultats de la cerca - Matthew Edwards

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  1. 1
    Evaluation of Satisfaction of Parents With the Use of Videoconferencing for a Pediatric Genetic Consultation

    Evaluation of Satisfaction of Parents With the Use of Videoconferencing for a Pediatric Genetic Consultation per Bruce Hopper, Melissa Buckman, Matthew Edwards

    Publicat 2011
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  2. 2
    The Impact of Huntington's Disease on Family Life

    The Impact of Huntington's Disease on Family Life per Marina Vamos, John Hambridge, Matthew Edwards, John Conaghan

    Publicat 2007
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  3. 3
    Identifying students faking ADHD: Preliminary findings and strategies for detection

    Identifying students faking ADHD: Preliminary findings and strategies for detection per Andrew Harrison, Matthew Edwards, Kevin C. H. Parker

    Publicat 2007
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  4. 4
    Rapid Activation of Spleen Dendritic Cell Subsets following Lymphocytic Choriomeningitis Virus Infection of Mice: Analysis of the Involvement of Type 1 IFN

    Rapid Activation of Spleen Dendritic Cell Subsets following Lymphocytic Choriomeningitis Virus Infection of Mice: Analysis of the Involvement of Type 1 IFN per María Montoya, Matthew Edwards, Delyth M. Reid, Persephone Borrow

    Publicat 2005
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  5. 5
    Recurrence of lethal osteogenesis imperfecta due to parental mosaicism for a mutation in the COL1A2 gene of type I collagen. The mosiac parent exhibits phenotypic features of a mild form of the disease

    Recurrence of lethal osteogenesis imperfecta due to parental mosaicism for a mutation in the COL1A2 gene of type I collagen. The mosiac parent exhibits phenotypic features of a mil... per Matthew Edwards, Richard Wenstrup, Peter H. Byers, Daniel H. Cohn

    Publicat 1992
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  6. 6
    GDF5 Is a Second Locus for Multiple-Synostosis Syndrome

    GDF5 Is a Second Locus for Multiple-Synostosis Syndrome per Katherine Dawson, Petra Seeman, Eiman Sebald, Lily King, Matthew Edwards, John Williams, Stefan Mundlos, Deborah Krakow

    Publicat 2006
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  7. 7
    Indications for Corneal Transplantation in New Zealand: 1991–1999

    Indications for Corneal Transplantation in New Zealand: 1991–1999 per Matthew Edwards, Gillian M. Clover, Nigel H Brookes, David Pendergrast, Jayne Chaulk, Charles N. J. McGhee

    Publicat 2002
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  8. 8
    Atrx deficiency induces telomere dysfunction, endocrine defects, and reduced life span

    Atrx deficiency induces telomere dysfunction, endocrine defects, and reduced life span per L. Ashley Watson, Lauren A. Solomon, Jennifer Ruizhe Li, Yan Jiang, Matthew Edwards, Kazuo Shin‐ya, Frank Beier, Nathalie G. Bérubé

    Publicat 2013
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  9. 9
    The Sphingosine 1-Phosphate Receptor Agonist FTY720 Differentially Affects the Sequestration of CD4+/CD25+ T-Regulatory Cells and Enhances Their Functional Activity

    The Sphingosine 1-Phosphate Receptor Agonist FTY720 Differentially Affects the Sequestration of CD4+/CD25+ T-Regulatory Cells and Enhances Their Functional Activity per Elżbieta Sawicka, Gerald Dubois, Gábor Járai, Matthew Edwards, Matthew J. Thomas, Andy Nicholls, Rainer Albert, Catherine Newson, Volker Brinkmann, Christoph Walker

    Publicat 2005
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  10. 10
    SCAI Technical Review on Management of Chronic Venous Disease

    SCAI Technical Review on Management of Chronic Venous Disease per Robert Attaran, Matthew Edwards, Matthew C. Bunte, Yulanka Castro‐Dominguez, Eri Fukaya, Karem Harth, Pamela Kim, Scott Firestone, Emily Senerth, Rebecca L. Morgan

    Publicat 2025
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  11. 11
    Barrier Disrupting Effects of Alternaria Alternata Extract on Bronchial Epithelium from Asthmatic Donors

    Barrier Disrupting Effects of Alternaria Alternata Extract on Bronchial Epithelium from Asthmatic Donors per Marina Leino, Matthew Loxham, Cornelia Blume, Emily J. Swindle, Nivenka Jayasekera, Patrick Dennison, Betty Shamji, Matthew Edwards, Stephen T. Holgate, Peter Howarth, Donna E. Davies

    Publicat 2013
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  12. 12
    Effect of Corneal Cross-linking versus Standard Care on Keratoconus Progression in Young Patients

    Effect of Corneal Cross-linking versus Standard Care on Keratoconus Progression in Young Patients per Frank Larkin, Kashfia Chowdhury, Jennifer Burr, Mathew K. Raynor, Matthew Edwards, Stephen J. Tuft, Catey Bunce, Emilia Caverly, Caroline J Doré, Susmito Biswas, Catey Bunce, Jennifer Burr, Emilia Caverly, Kashfia Chowdhury, Caroline J Doré, Matthew Edwards, L French, Stephen B. Kaye, Anne Klepacz, Dimitra Kopsini, Frank Larkin, Mathew K. Raynor, Stephen J. Tuft, Sue Webber, Colin E. Willoughby

    Publicat 2021
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  13. 13
    EMQN: Recommendations for genetic testing in inherited cardiomyopathies and arrhythmias

    EMQN: Recommendations for genetic testing in inherited cardiomyopathies and arrhythmias per Jesse B.G. Hayesmoore, Zahurul A. Bhuiyan, Domenico Coviello, Desirée du Sart, Matthew Edwards, Maria Iascone, Deborah Morris‐Rosendahl, Katie Sheils, Marjon van Slegtenhorst, Kate Thomson

    Publicat 2023
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  14. 14
    Convergence of YAP/TAZ, TEAD and TP63 activity is associated with bronchial premalignant severity and progression

    Convergence of YAP/TAZ, TEAD and TP63 activity is associated with bronchial premalignant severity and progression per Boting Ning, Andrew Tilston-Lünel, Justice Simonetti, Julia Hicks‐Berthet, Adeline Matschulat, Roxana Pfefferkorn, Avrum Spira, Matthew Edwards, Sarah A. Mazzilli, Marc E. Lenburg, Jennifer Beane, Xaralabos Varelas

    Publicat 2023
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  15. 15
    Expression and Cellular Provenance of Thymic Stromal Lymphopoietin and Chemokines in Patients with Severe Asthma and Chronic Obstructive Pulmonary Disease

    Expression and Cellular Provenance of Thymic Stromal Lymphopoietin and Chemokines in Patients with Severe Asthma and Chronic Obstructive Pulmonary Disease per Sun Ying, Brian O’Connor, Jonathan Ratoff, Qiu Meng, Cailong Fang, David J. Cousins, Guizhen Zhang, Shuyan Gu, Zhongli Gao, Betty Shamji, Matthew Edwards, TH Lee, Christopher J. Corrigan

    Publicat 2008
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  16. 16
    Integrated genome and transcriptome analyses reveal the mechanism of genome instability in ataxia with oculomotor apraxia 2

    Integrated genome and transcriptome analyses reveal the mechanism of genome instability in ataxia with oculomotor apraxia 2 per Radhakrishnan Kanagaraj, Richard Mitter, Theodoros Kantidakis, Matthew Edwards, Anaid Benitez, Probir Chakravarty, Beiyuan Fu, Olivier J. Bécherel, Fengtang Yang, Martin F. Lavin, Amnon Koren, Aengus Stewart, Stephen C. West

    Publicat 2022
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  17. 17
    Treatment with Anti–Gremlin 1 Antibody Ameliorates Chronic Hypoxia/SU5416–Induced Pulmonary Arterial Hypertension in Mice

    Treatment with Anti–Gremlin 1 Antibody Ameliorates Chronic Hypoxia/SU5416–Induced Pulmonary Arterial Hypertension in Mice per Loredana Ciuclan, Kelly-Ann Sheppard, Liqun Dong, Daniel Sutton, Nicholas Duggan, Martin Hussey, Jenny Simmons, Nicholas W. Morrell, Gábor Járai, Matthew Edwards, Gerald Dubois, Matthew J. Thomas, Gino Van Heeke, Karen England

    Publicat 2013
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  18. 18
    Defective B cell responses in the absence of SH2D1A

    Defective B cell responses in the absence of SH2D1A per Massimo Morra, Robert A. Barrington, Ana Clara Abadía‐Molina, Susumo Okamoto, Aimée Julien, Charles Gullo, Anuj Kalsy, Matthew Edwards, Gang Chen, Rosanne Spolski, Warren J. Leonard, Brigitte T. Huber, Persephone Borrow, Christine A. Biron, Abhay R. Satoskar, Michael C. Carroll, Cox Terhorst

    Publicat 2005
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  19. 19
    CardioClassifier: disease- and gene-specific computational decision support for clinical genome interpretation

    CardioClassifier: disease- and gene-specific computational decision support for clinical genome interpretation per Nicola Whiffin, Roddy Walsh, Risha Govind, Matthew Edwards, Mian Ahmad, Xiaolei Zhang, Upasana Tayal, Rachel Buchan, William Midwinter, Alicja Wilk, Hanna Najgebauer, Catherine Francis, Sam Wilkinson, Thomas Monk, Laura Brett, Declan P. O’Regan, Sanjay Prasad, Deborah Morris‐Rosendahl, Paul J.R. Barton, Elizabeth Edwards, James S. Ware, Stuart A. Cook

    Publicat 2018
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  20. 20
    Multi-model functionalization of disease-associated PTEN missense mutations identifies multiple molecular mechanisms underlying protein dysfunction

    Multi-model functionalization of disease-associated PTEN missense mutations identifies multiple molecular mechanisms underlying protein dysfunction per Kathryn Post, Manuel Belmadani, Payel Ganguly, Fabian Meili, Riki Dingwall, Troy A. McDiarmid, Warren M. Meyers, Caitlin Herrington, Barry P. Young, Daniel B. Callaghan, Sanja Rogić, Matthew Edwards, Ana Nićiforović, Alessandro Cau, Catharine H. Rankin, Timothy P. O’Connor, Shernaz X. Bamji, Christopher Loewen, Douglas W. Allan, Paul Pavlidis, Kurt Haas

    Publicat 2020
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