Arama Sonuçları - Diana Johnson

Sonuçları Daraltın
  1. 1
    Human pregnancy safety for agents used to treat rheumatoid arthritis: adequacy of available information and strategies for developing post-marketing data.

    Human pregnancy safety for agents used to treat rheumatoid arthritis: adequacy of available information and strategies for developing post-marketing data. Yazar: Christina Chambers, Zuhre Tutuncu, Diana Johnson, Kenneth L. Jones

    Baskı/Yayın Bilgisi 2006
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  2. 2
    ANTAGONISM OF EXCITATORY AMINO ACID‐INDUCED RESPONSES AND OF SYNAPTIC EXCITATION IN THE ISOLATED SPINAL CORD OF THE FROG

    ANTAGONISM OF EXCITATORY AMINO ACID‐INDUCED RESPONSES AND OF SYNAPTIC EXCITATION IN THE ISOLATED SPINAL CORD OF THE FROG Yazar: Richard H. Evans, A. A. Francis, K Hunt, Diana Johnson Oakes, J.C. Watkins

    Baskı/Yayın Bilgisi 1979
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  3. 3
    Selective depression of excitatory amino acid induced depolarizations by magnesium ions in isolated spinal cord preparations.

    Selective depression of excitatory amino acid induced depolarizations by magnesium ions in isolated spinal cord preparations. Yazar: Brian Ault, Richard H. Evans, A. A. Francis, Diana Johnson Oakes, J.C. Watkins

    Baskı/Yayın Bilgisi 1980
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  4. 4
    Hyperglycemia in the Posttransplant Period: NODAT vs Posttransplant Diabetes Mellitus

    Hyperglycemia in the Posttransplant Period: NODAT vs Posttransplant Diabetes Mellitus Yazar: Gupta, Suruchi, Pollack, Teresa, Fulkerson, Candice, Schmidt, Kathleen, Oakes, Diana Johnson, Molitch, Mark E, Wallia, Amisha

    Baskı/Yayın Bilgisi 2018
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  5. 5
    Donor treatment with pegylated G-CSF augments the generation of IL-10-producing regulatory T cells and promotes transplantation tolerance

    Donor treatment with pegylated G-CSF augments the generation of IL-10-producing regulatory T cells and promotes transplantation tolerance Yazar: Edward S. Morris, Kelli P. A. MacDonald, Vanessa Rowe, Diana Johnson, Tatjana Banovic, Andrew D. Clouston, Geoffrey R. Hill

    Baskı/Yayın Bilgisi 2004
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  6. 6
    Outcome following high-dose methotrexate in pregnancies misdiagnosed as ectopic

    Outcome following high-dose methotrexate in pregnancies misdiagnosed as ectopic Yazar: Laila Nurmohamed, Myla E. Moretti, Tal Schechter, Adrienne Einarson, Diana Johnson, Sharon Voyer Lavigne, Aida Erebara, Gideon Koren, Yaron Finkelstein

    Baskı/Yayın Bilgisi 2011
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  7. 7
    Anterior thalamic lesions stop synaptic plasticity in retrosplenial cortex slices: expanding the pathology of diencephalic amnesia

    Anterior thalamic lesions stop synaptic plasticity in retrosplenial cortex slices: expanding the pathology of diencephalic amnesia Yazar: Derek L.F. Garden, Peter V. Massey, Douglas A. Caruana, Diana Johnson, Elizabeth C. Warburton, John P. Aggleton, Zafar I. Bashir

    Baskı/Yayın Bilgisi 2009
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  8. 8
    A novel method for detecting uniparental disomy from trio genotypes identifies a significant excess in children with developmental disorders

    A novel method for detecting uniparental disomy from trio genotypes identifies a significant excess in children with developmental disorders Yazar: Daniel A. King, Tomas Fitzgerald, Ray Miller, Natalie Canham, Jill Clayton‐Smith, Diana Johnson, Sahar Mansour, Fiona Stewart, Pradeep Vasudevan, Matthew E. Hurles

    Baskı/Yayın Bilgisi 2013
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  9. 9
    Diagnosis, natural history, and management in vascular Ehlers–Danlos syndrome

    Diagnosis, natural history, and management in vascular Ehlers–Danlos syndrome Yazar: Peter H. Byers, John W. Belmont, James H. Black, Julie De Backer, Michael Frank, Xavier Jeunemaı̂tre, Diana Johnson, Melanie Pepin, Leema Robert, Lynn Sanders, Nigel Wheeldon

    Baskı/Yayın Bilgisi 2017
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  10. 10
    Diagnosis and management of vascular Ehlers-Danlos syndrome: Experience of the UK national diagnostic service, Sheffield

    Diagnosis and management of vascular Ehlers-Danlos syndrome: Experience of the UK national diagnostic service, Sheffield Yazar: Jessica Bowen, Mónica Hernández Alava, Diana Johnson, Claire Green, Tammy Kammin, Duncan Baker, Sylvia Keigwin, Seiko Makino, Naomi Taylor, Oliver J. Watson, Nigel Wheeldon, Glenda Sobey

    Baskı/Yayın Bilgisi 2023
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  11. 11
    Mass Spectrometry-Based Direct Sequencing of tRNAs De Novo and Quantitative Mapping of Multiple RNA Modifications

    Mass Spectrometry-Based Direct Sequencing of tRNAs De Novo and Quantitative Mapping of Multiple RNA Modifications Yazar: Xiaohong Yuan, Yue Su, Diana Johnson, Michele Kirchner, Xu Dong Zhang, Sihang Xu, S. H. Jiang, Kaichun Wu, Shundi Shi, James J. Russo, Qi Chen, Shenglong Zhang

    Baskı/Yayın Bilgisi 2024
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  12. 12
    Mutations in <i>CHD7</i> in patients with CHARGE syndrome cause T–B + natural killer cell + severe combined immune deficiency and may cause Omenn-like syndrome

    Mutations in <i>CHD7</i> in patients with CHARGE syndrome cause T–B + natural killer cell + severe combined immune deficiency and may cause Omenn-like syndrome Yazar: Andrew R. Gennery, Mary Slatter, Jason Rice, Lies H. Hoefsloot, D Barge, Andrew McLean‐Tooke, Tara Montgomery, JA Goodship, Alastair D. Burt, Terry Flood, Mario Abinun, A J Cant, Diana Johnson

    Baskı/Yayın Bilgisi 2008
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  13. 13
    Glycemic Control Reduces Infections in Post–Liver Transplant Patients: Results of a Prospective, Randomized Study

    Glycemic Control Reduces Infections in Post–Liver Transplant Patients: Results of a Prospective, Randomized Study Yazar: Wallia, Amisha, Schmidt, Kathleen, Oakes, Diana Johnson, Pollack, Teresa, Welsh, Nicholas, Kling-Colson, Susan, Gupta, Suruchi, Fulkerson, Candice, Aleppo, Grazia, Parikh, Neehar, Levitsky, Josh, Norvell, J. P., Rademaker, Alfred, Molitch, Mark E.

    Baskı/Yayın Bilgisi 2016
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  14. 14
    Mutations in MEF2C from the 5q14.3q15 microdeletion syndrome region are a frequent cause of severe mental retardation and diminish MECP2 and CDKL5 expression

    Mutations in MEF2C from the 5q14.3q15 microdeletion syndrome region are a frequent cause of severe mental retardation and diminish MECP2 and CDKL5 expression Yazar: Markus Zweier, Anne Gregor, Christiane Zweier, Hartmut Engels, Heinrich Sticht, Eva Wohlleber, Emilia K. Bijlsma, Susan Holder, Martin Zenker, Eva Rossier, Ute Grasshoff, Diana Johnson, Lisa Robertson, Helen V. Firth, Cornelia Kraus, Arif B. Ekici, André Reis, Anita Rauch

    Baskı/Yayın Bilgisi 2010
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  15. 15
    Analysis of exome data for 4293 trios suggests GPI-anchor biogenesis defects are a rare cause of developmental disorders

    Analysis of exome data for 4293 trios suggests GPI-anchor biogenesis defects are a rare cause of developmental disorders Yazar: Alistair T. Pagnamenta, Yoshiko Murakami, John Taylor, Consuelo Anzilotti, Malcolm F. Howard, Venessa Miller, Diana Johnson, Shereen Tadros, Sahar Mansour, I. Karen Temple, Rachel Firth, Elisabeth Rosser, Rachel Harrison, Bronwen Kerr, Niko Popitsch, Taroh Kinoshita, Jenny C. Taylor, Usha Kini

    Baskı/Yayın Bilgisi 2017
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  16. 16
    Absence of Heterozygosity Due to Template Switching during Replicative Rearrangements

    Absence of Heterozygosity Due to Template Switching during Replicative Rearrangements Yazar: Claudia M.B. Carvalho, Rolph Pfundt, Daniel A. King, Sarah Lindsay, Luciana W. Zuccherato, Merryn Macville, Pengfei Liu, Diana Johnson, Paweł Stankiewicz, Chester Brown, Chad A. Shaw, Matthew E. Hurles, Grzegorz Ira, P. J. Hastings, Han G. Brunner, James R. Lupski

    Baskı/Yayın Bilgisi 2015
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  17. 17
    White Paper Report of the RAD-AID Conference on International Radiology for Developing Countries: Identifying Challenges, Opportunities, and Strategies for Imaging Services in the Developing World

    White Paper Report of the RAD-AID Conference on International Radiology for Developing Countries: Identifying Challenges, Opportunities, and Strategies for Imaging Services in the... Yazar: Daniel J. Mollura, Ezana M. Azene, Anna Starikovsky, Aduke Thelwell, Sarah Iosifescu, Cary Kimble, Ann Polin, Brian S. Garra, Kristen DeStigter, Brad Short, Diana Johnson, Christian S Welch, Ivy Walker, David M. White, Mehrbod S. Javadi, Matthew P. Lungren, Atif Zaheer, Barry B. Goldberg, Jonathan S. Lewin

    Baskı/Yayın Bilgisi 2010
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  18. 18
    Missense Variants in RHOBTB2 Cause a Developmental and Epileptic Encephalopathy in Humans, and Altered Levels Cause Neurological Defects in Drosophila

    Missense Variants in RHOBTB2 Cause a Developmental and Epileptic Encephalopathy in Humans, and Altered Levels Cause Neurological Defects in Drosophila Yazar: Jonas Straub, Enrico D.H. Konrad, Johanna Grüner, Annick Toutain, Levinus A. Bok, Megan T. Cho, Heather P. Crawford, Holly Dubbs, Ganka Douglas, Rebekah Jobling, Diana Johnson, Bryan L. Krock, Mohamad A. Mikati, Addie I. Nesbitt, Joost Nicolai, Meredith Phillips, Annapurna Poduri, Xilma R. Ortiz‐González, Zöe Powis, Avni Santani, Lacey Smith, Alexander P.A. Stegmann, Constance T. R. M. Stumpel, Maaike Vreeburg, Anna Fliedner, Anne Gregor, Heinrich Sticht, Christiane Zweier

    Baskı/Yayın Bilgisi 2017
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  19. 19
    The phenotypic spectrum of WWOX-related disorders: 20 additional cases of WOREE syndrome and review of the literature

    The phenotypic spectrum of WWOX-related disorders: 20 additional cases of WOREE syndrome and review of the literature Yazar: Juliette Piard, Lara Hawkes, Mathieu Milh, Laurent Villard, Renato Borgatti, Romina Romaniello, Mélanie Fradin, Yline Capri, Delphine Héron, Marie‐Christine Nouguès, Caroline Nava, Oana Tarta Arsene, Debbie Shears, John Taylor, Alistair T. Pagnamenta, Jenny C. Taylor, Yoshimi Sogawa, Diana Johnson, Helen V. Firth, Pradeep Vasudevan, Gabriela Jones, Marie-Ange Nguyen-Morel, Tiffany Busa, Agathe Roubertie, Myrthe van den Born, Elise Brischoux‐Boucher, M. Kœnig, Cyril Mignot, Usha Kini, Christophe Philippe

    Baskı/Yayın Bilgisi 2018
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  20. 20
    Pathogenicity and selective constraint on variation near splice sites

    Pathogenicity and selective constraint on variation near splice sites Yazar: Jenny Lord, Giuseppe Gallone, Patrick Short, Jeremy F. McRae, Holly Ironfield, Elizabeth Wynn, Sebastian S. Gerety, Liu He, Bronwyn Kerr, Diana Johnson, Emma McCann, Esther Kinning, Frances Flinter, I. Karen Temple, Jill Clayton‐Smith, Meriel McEntagart, Sally Ann Lynch, Shelagh Joss, Sofia Douzgou, Tabib Dabir, Virginia Clowes, Vivienne McConnell, Wayne Lam, Caroline F. Wright, David Fitzpatrick, Helen V. Firth, Jeffrey C. Barrett, Matthew E. Hurles

    Baskı/Yayın Bilgisi 2018
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