Αποτελέσματα αναζήτησης - Cleo C. van Diemen

Περιορισμός αποτελεσμάτων
  1. 1
    A next-generation sequencing method for gene doping detection that distinguishes low levels of plasmid DNA against a background of genomic DNA

    A next-generation sequencing method for gene doping detection that distinguishes low levels of plasmid DNA against a background of genomic DNA από Eddy N. de Boer, Petra E. van der Wouden, Lennart Johansson, Cleo C. van Diemen, Hidde J. Haisma

    Έκδοση 2019
    Λήψη πλήρους κειμένου Λήψη πλήρους κειμένου
    Artigo
    Προσθήκη στα αγαπημένα
    Αποθηκεύτηκε σε:
  2. 2
    Restricted IgA Repertoire in Both B-1 and B-2 Cell-Derived Gut Plasmablasts

    Restricted IgA Repertoire in Both B-1 and B-2 Cell-Derived Gut Plasmablasts από Maaike Stoel, Han-Qing Jiang, Cleo C. van Diemen, Judy C. A. M. Bun, Peter M. Dammers, M. Christine Thurnheer, Frans G. M. Kroese, John J. Cebra, Nicolaas A. Bos

    Έκδοση 2005
    Λήψη πλήρους κειμένου Λήψη πλήρους κειμένου
    Artigo
    Προσθήκη στα αγαπημένα
    Αποθηκεύτηκε σε:
  3. 3
    Occupational exposure to pesticides is associated with differential DNA methylation

    Occupational exposure to pesticides is associated with differential DNA methylation από Diana A. van der Plaat, Kim de Jong, Maaike de Vries, Cleo C. van Diemen, Ivana Nedeljković, Najaf Amin, Hans Kromhout, Roel Vermeulen, Dirkje S. Postma, Cornelia M. van Duijn, H. Marike Boezen, Judith M. Vonk

    Έκδοση 2018
    Λήψη πλήρους κειμένου Λήψη πλήρους κειμένου
    Artigo
    Προσθήκη στα αγαπημένα
    Αποθηκεύτηκε σε:
  4. 4
    From blood to lung tissue: effect of cigarette smoke on DNA methylation and lung function

    From blood to lung tissue: effect of cigarette smoke on DNA methylation and lung function από Maaike de Vries, Diana A. van der Plaat, Ivana Nedeljković, Rikst Nynke Verkaik‐Schakel, Wierd Kooistra, Najaf Amin, Cornelia M. van Duijn, Corry‐Anke Brandsma, Cleo C. van Diemen, Judith M. Vonk, H. Marike Boezen

    Έκδοση 2018
    Λήψη πλήρους κειμένου Λήψη πλήρους κειμένου
    Artigo
    Προσθήκη στα αγαπημένα
    Αποθηκεύτηκε σε:
  5. 5
    GAVIN: Gene-Aware Variant INterpretation for medical sequencing

    GAVIN: Gene-Aware Variant INterpretation for medical sequencing από K. Joeri van der Velde, Eddy N. de Boer, Cleo C. van Diemen, Birgit Sikkema‐Raddatz, Kristin M. Abbott, Alain Knopperts, Lude Franke, Rolf H. Sijmons, Tom J. de Koning, Cisca Wijmenga, Richard J. Sinke, Morris A. Swertz

    Έκδοση 2017
    Λήψη πλήρους κειμένου Λήψη πλήρους κειμένου
    Artigo
    Προσθήκη στα αγαπημένα
    Αποθηκεύτηκε σε:
  6. 6
    <i>MEFV</i>mutations affecting pyrin amino acid 577 cause autosomal dominant autoinflammatory disease

    <i>MEFV</i>mutations affecting pyrin amino acid 577 cause autosomal dominant autoinflammatory disease από Monique Stoffels, Agata Szperl, Anna Simon, Mihai G. Netea, Theo S. Plantinga, Marcel van Deuren, Sylvia Kamphuis, Helen J. Lachmann, Edwin Cuppen, Wigard P. Kloosterman, Joost Frenkel, Cleo C. van Diemen, Cisca Wijmenga, Mariëlle van Gijn, Jos W.M. van der Meer

    Έκδοση 2013
    Λήψη πλήρους κειμένου
    Artigo
    Προσθήκη στα αγαπημένα
    Αποθηκεύτηκε σε:
  7. 7
    A prospective study on rapid exome sequencing as a diagnostic test for multiple congenital anomalies on fetal ultrasound

    A prospective study on rapid exome sequencing as a diagnostic test for multiple congenital anomalies on fetal ultrasound από Nicole Corsten‐Janssen, Katelijne Bouman, Janouk C. D. Diphoorn, Arjen J. Scheper, R. Kinds, Julia el Mecky, Hanna Breet, Joanne Verheij, Ron F. Suijkerbuijk, L. Duin, G. T. R. Manten, Irene M. van Langen, Rolf H. Sijmons, Birgit Sikkema‐Raddatz, Helga Westers, Cleo C. van Diemen

    Έκδοση 2020
    Λήψη πλήρους κειμένου Λήψη πλήρους κειμένου
    Artigo
    Προσθήκη στα αγαπημένα
    Αποθηκεύτηκε σε:
  8. 8
    Genome-wide association study on the FEV 1 /FVC ratio in never-smokers identifies HHIP and FAM13A

    Genome-wide association study on the FEV 1 /FVC ratio in never-smokers identifies HHIP and FAM13A από Diana A. van der Plaat, Kim de Jong, Lies Lahousse, Alen Faiz, Judith M. Vonk, Cleo C. van Diemen, Ivana Nedeljković, Najaf Amin, Guy Brusselle, Albert Hofman, Corry‐Anke Brandsma, Yohan Bossé, Don D. Sin, David C. Nickle, Cornelia M. van Duijn, Dirkje S. Postma, H. Marike Boezen

    Έκδοση 2016
    Λήψη πλήρους κειμένου
    Revisão
    Προσθήκη στα αγαπημένα
    Αποθηκεύτηκε σε:
  9. 9
    Genetic Analysis of Innate Immunity in Crohn's Disease and Ulcerative Colitis Identifies Two Susceptibility Loci Harboring CARD9 and IL18RAP

    Genetic Analysis of Innate Immunity in Crohn's Disease and Ulcerative Colitis Identifies Two Susceptibility Loci Harboring CARD9 and IL18RAP από Alexandra Zhernakova, Eleonora A. Festen, Lude Franke, Gosia Trynka, Cleo C. van Diemen, Alienke J. Monsuur, Marianna R. Bevova, Rian M. Nijmeijer, Ruben van ‘t Slot, Roel Heijmans, H. Marike Boezen, David A. van Heel, Adriaan A. van Bodegraven, Pieter Stokkers, Cisca Wijmenga, J. Bart A. Crusius, Rinse K. Weersma

    Έκδοση 2008
    Λήψη πλήρους κειμένου Λήψη πλήρους κειμένου
    Artigo
    Προσθήκη στα αγαπημένα
    Αποθηκεύτηκε σε:
  10. 10
    CAPICE: a computational method for Consequence-Agnostic Pathogenicity Interpretation of Clinical Exome variations

    CAPICE: a computational method for Consequence-Agnostic Pathogenicity Interpretation of Clinical Exome variations από Shuang� Li, K. Joeri van der Velde, Dick de Ridder, Aalt D. J. van Dijk, Dimitrios Soudis, Leslie R. Zwerwer, Patrick Deelen, Dennis Hendriksen, Bart Charbon, Mariëlle van Gijn, Kristin M. Abbott, Birgit Sikkema‐Raddatz, Cleo C. van Diemen, Wilhelmina S. Kerstjens‐Frederikse, Richard J. Sinke, Morris A. Swertz

    Έκδοση 2020
    Λήψη πλήρους κειμένου Λήψη πλήρους κειμένου
    Artigo
    Προσθήκη στα αγαπημένα
    Αποθηκεύτηκε σε:
  11. 11
    Nanopore Long-Read Sequencing as a First-Tier Diagnostic Test to Detect Repeat Expansions in Neurological Disorders

    Nanopore Long-Read Sequencing as a First-Tier Diagnostic Test to Detect Repeat Expansions in Neurological Disorders από Eddy N. de Boer, Arjen J. Scheper, Dennis Hendriksen, Bart Charbon, Gerben van der Vries, Annelies M. ten Berge, P.M. Grootscholten, Henny H. Lemmink, Jan D.H. Jongbloed, Laura Bosscher, N. Knoers, Morris A. Swertz, Birgit Sikkema‐Raddatz, Dorieke J. Dijkstra, Lennart Johansson, Cleo C. van Diemen

    Έκδοση 2025
    Λήψη πλήρους κειμένου
    Artigo
    Προσθήκη στα αγαπημένα
    Αποθηκεύτηκε σε:
  12. 12
    The emerging landscape of dynamic DNA methylation in early childhood

    The emerging landscape of dynamic DNA methylation in early childhood από Cheng‐Jian Xu, Marc Jan Bonder, Cilla Söderhäll, Mariona Bustamante, Nour Baïz, Ulrike Gehring, Soesma A. Jankipersadsing, Pieter van der Vlies, Cleo C. van Diemen, Bianca van Rijkom, J. Just, Inger Kull, Juha Kere, Josep M. Antó, Jean Bousquet, Alexandra Zhernakova, Cisca Wijmenga, Isabella Annesi‐Maesano, Jordi Sunyer, Erik Melén, Yang Li, Dirkje S. Postma, Gerard H. Koppelman

    Έκδοση 2017
    Λήψη πλήρους κειμένου
    Artigo
    Προσθήκη στα αγαπημένα
    Αποθηκεύτηκε σε:
  13. 13
    Functional genomics identifies type I interferon pathway as central for host defense against Candida albicans

    Functional genomics identifies type I interferon pathway as central for host defense against Candida albicans από Sanne P. Smeekens, Aylwin Ng, Vinod Kumar, Melissa D. Johnson, Theo S. Plantinga, Cleo C. van Diemen, Peer Arts, Eugène T.P. Verwiel, Mark S. Gresnigt, Karin Fransén, Suzanne van Sommeren, Marije Oosting, Shih‐Chin Cheng, Leo A. B. Joosten, Alexander Hoischen, Bart Jan Kullberg, William K. Scott, John R. Perfect, J.W.M. van der Meer, Cisca Wijmenga, Mihai G. Netea, Ramnik J. Xavier

    Έκδοση 2013
    Λήψη πλήρους κειμένου Λήψη πλήρους κειμένου
    Artigo
    Προσθήκη στα αγαπημένα
    Αποθηκεύτηκε σε:
  14. 14
    Identification of <i>PCDH1</i> as a Novel Susceptibility Gene for Bronchial Hyperresponsiveness

    Identification of <i>PCDH1</i> as a Novel Susceptibility Gene for Bronchial Hyperresponsiveness από Gerard H. Koppelman, Deborah A. Meyers, Timothy D. Howard, Shun Zheng, Greg Hawkins, Elizabeth J. Ampleford, Jianfeng Xu, Henk Koning, Marcel Bruinenberg, Ilja M. Nolte, Cleo C. van Diemen, H. Marike Boezen, Wim Timens, Paul A. Whittaker, O. Colin Stine, Sheila J. Barton, John W. Holloway, Stephen T. Holgate, Penelope E. Graves, Fernando D. Martínez, Antoon J. van Oosterhout, Eugene R. Bleecker, Dirkje S. Postma

    Έκδοση 2009
    Λήψη πλήρους κειμένου
    Artigo
    Προσθήκη στα αγαπημένα
    Αποθηκεύτηκε σε:
  15. 15
    Rapid Targeted Genomics in Critically Ill Newborns

    Rapid Targeted Genomics in Critically Ill Newborns από Cleo C. van Diemen, Wilhelmina S. Kerstjens‐Frederikse, Klasien A. Bergman, Tom J. de Koning, Birgit Sikkema‐Raddatz, Joeri K. van der Velde, Kristin M. Abbott, Johanna C. Herkert, Katharina Löhner, Patrick Rump, Martine T. Meems-Veldhuis, Pieter B. Neerincx, Jan D.H. Jongbloed, Conny M.A. van Ravenswaaij‐Arts, Morris A. Swertz, Richard J. Sinke, Irene M. van Langen, Cisca Wijmenga

    Έκδοση 2017
    Λήψη πλήρους κειμένου
    Artigo
    Προσθήκη στα αγαπημένα
    Αποθηκεύτηκε σε:
  16. 16
    Improving coeliac disease risk prediction by testing non-HLA variants additional to HLA variants

    Improving coeliac disease risk prediction by testing non-HLA variants additional to HLA variants από Jihane Romanos, Anna Rosén, Vinod Kumar, Gosia Trynka, Lude Franke, Agata Szperl, Javier Gutierrez‐Achury, Cleo C. van Diemen, Roan Kanninga, Soesma A. Jankipersadsing, Andrea K. Steck, Georges Eisenbarth, David A. van Heel, Božena Cukrowská, Valentina Bruno, Maria Cristina Mazzilli, Concepción Núñez, José Ramón Bilbao, M. L. Mearin, Donatella Barisani, Marian Rewers, Jill M. Norris, Anneli Ivarsson, H. Marieke Boezen, Edwin Liu, Cisca Wijmenga

    Έκδοση 2013
    Λήψη πλήρους κειμένου Λήψη πλήρους κειμένου
    Artigo
    Προσθήκη στα αγαπημένα
    Αποθηκεύτηκε σε:
  17. 17
    Exome sequencing and network analysis identifies shared mechanisms underlying spinocerebellar ataxia

    Exome sequencing and network analysis identifies shared mechanisms underlying spinocerebellar ataxia από Esther Nibbeling, Anna Duarri, Corien C. Verschuuren‐Bemelmans, Michiel R. Fokkens, Juha Karjalainen, Cleo J. L. M. Smeets, Jelkje J. de Boer-Bergsma, Gerben van der Vries, Dennis Dooijes, Giovana Bampi, Cleo C. van Diemen, E. R. Brunt, Elly F. Ippel, Berry Kremer, Monique H.M. Vlak, Noam Adir, Cisca Wijmenga, Bart P.C. van de Warrenburg, Lude Franke, Richard J. Sinke, Dineke S. Verbeek

    Έκδοση 2017
    Λήψη πλήρους κειμένου Λήψη πλήρους κειμένου
    Artigo
    Προσθήκη στα αγαπημένα
    Αποθηκεύτηκε σε:
  18. 18
    Common and different genetic background for rheumatoid arthritis and coeliac disease

    Common and different genetic background for rheumatoid arthritis and coeliac disease από Marieke J. H. Coenen, Gosia Trynka, Sandra Heskamp, Barbara Franke, Cleo C. van Diemen, Joanna Smolonska, Miek van Leeuwen, Elisabeth Brouwer, Marike Boezen, Dirkje S. Postma, Mathieu Platteel, Pieter Zanen, Jan-Willem W.J. Lammers, Harry J.M. Groen, Willem P.T.M. Mali, Chris J. Mulder, Greetje J. Tack, Wieke H.M. Verbeek, Victorien M. Wolters, Roderick H.J. Houwen, M. Luisa Mearin, David A. van Heel, Timothy R. D. J. Radstake, Piet L. C. M. van Riel, Cisca Wijmenga, Pilar Barrera, Alexandra Zhernakova

    Έκδοση 2009
    Λήψη πλήρους κειμένου
    Artigo
    Προσθήκη στα αγαπημένα
    Αποθηκεύτηκε σε:
  19. 19
    Improving the diagnostic yield of exome- sequencing by predicting gene–phenotype associations using large-scale gene expression analysis

    Improving the diagnostic yield of exome- sequencing by predicting gene–phenotype associations using large-scale gene expression analysis από Patrick Deelen, Sipko van Dam, Johanna C. Herkert, Juha Karjalainen, Harm Brugge, Kristin M. Abbott, Cleo C. van Diemen, Paul A. van der Zwaag, Erica H. Gerkes, Evelien Zonneveld‐Huijssoon, Jelkje J. de Boer-Bergsma, Pytrik Folkertsma, Tessa E. Gillett, K. Joeri van der Velde, Roan Kanninga, Peter C. van den Akker, Sabrina Z. Jan, Edgar T. Hoorntje, Wouter P. te Rijdt, Yvonne J. Vos, Jan D.H. Jongbloed, Conny M.A. van Ravenswaaij‐Arts, Richard J. Sinke, Birgit Sikkema‐Raddatz, Wilhelmina S. Kerstjens‐Frederikse, Morris A. Swertz, Lude Franke

    Έκδοση 2019
    Λήψη πλήρους κειμένου Λήψη πλήρους κειμένου
    Artigo
    Προσθήκη στα αγαπημένα
    Αποθηκεύτηκε σε:
  20. 20
    Common Variants in the Type 2 Diabetes KCNQ1 Gene Are Associated with Impairments in Insulin Secretion During Hyperglycaemic Glucose Clamp

    Common Variants in the Type 2 Diabetes KCNQ1 Gene Are Associated with Impairments in Insulin Secretion During Hyperglycaemic Glucose Clamp από Jana V. van Vliet‐Ostaptchouk, Timon W. van Haeften, Gijs W.D. Landman, Erwin Reiling, Nanne Kleefstra, Henk J.G. Bilo, Olaf H. Klungel, Anthonius de Boer, Cleo C. van Diemen, Cisca Wijmenga, H. Marike Boezen, Joost Dekker, Esther van ‘t Riet, Giel Nijpels, Laura M.C. Welschen, Hata Zavrelova, Elinda J. Bruin, Clara C. Elbers, Florianne Bauer, N. Charlotte Onland‐Moret, Yvonne T. van der Schouw, Diederick E. Grobbee, Annemieke M. W. Spijkerman, Daphne L. van der A, Annemarie M. Simonis-Bik, Elisabeth M. W. Eekhoff, Michaëla Diamant, Mark H.H. Kramer, Dorret I. Boomsma, Eco J. C. de Geus, Gonneke Willemsen, P. Eline Slagboom, Marten H. Hofker, Leen M. ’t Hart

    Έκδοση 2012
    Λήψη πλήρους κειμένου Λήψη πλήρους κειμένου
    Artigo
    Προσθήκη στα αγαπημένα
    Αποθηκεύτηκε σε:

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