检索结果 - Ulrich Broeckel

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  1. 1
    Pediatric inflammatory bowel disease: Clinical and molecular genetics

    Pediatric inflammatory bowel disease: Clinical and molecular genetics 由 Vincent Biank, Ulrich Broeckel, Subra Kugathasan

    出版 2007
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  2. 2
    Left-ventricular dysfunction

    Left-ventricular dysfunction 由 Heribert Schunkert, Ulrich Broeckel, Hans W. Hense, Ulrich Keil, G. Riegger

    出版 1998
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  3. 3
    Comprehensive evaluation of AmpliSeq transcriptome, a novel targeted whole transcriptome RNA sequencing methodology for global gene expression analysis

    Comprehensive evaluation of AmpliSeq transcriptome, a novel targeted whole transcriptome RNA sequencing methodology for global gene expression analysis 由 Wenli Li, Amy Turner, Praful Aggarwal, Andrea Matter, Erin Storvick, Donna K. Arnett, Ulrich Broeckel

    出版 2015
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  4. 4
    An Autoinflammatory Disease Due to Homozygous Deletion of the<i>IL1RN</i>Locus

    An Autoinflammatory Disease Due to Homozygous Deletion of the<i>IL1RN</i>Locus 由 Sreelatha T. Reddy, Shuang Jia, Rhonda Geoffrey, Rachel Lorier, Mariko Suchi, Ulrich Broeckel, Martin J. Hessner, James Verbsky

    出版 2009
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  5. 5
    Clinical, Genetic and Environmental Factors Associated with Congenital Vertebral Malformations

    Clinical, Genetic and Environmental Factors Associated with Congenital Vertebral Malformations 由 Philip F. Giampietro, Cathy Raggio, Robert D. Blank, Catherine A. McCarty, Ulrich Broeckel, Michael A. Pickart

    出版 2012
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  6. 6
    The associations of body size and body composition with left ventricular mass: impacts for indexation in adults

    The associations of body size and body composition with left ventricular mass: impacts for indexation in adults 由 Hans‐Werner Hense, Birgit Gneiting, M Muscholl, Ulrich Broeckel, Bernhard Kuch, Angela Doering, Günter A.J. Riegger, Heribert Schunkert

    出版 1998
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  7. 7
    Whole‐genome copy number variation analysis in anophthalmia and microphthalmia

    Whole‐genome copy number variation analysis in anophthalmia and microphthalmia 由 KF Schilter, Linda M. Reis, Adele Schneider, TM Bardakjian, Omar Abdul‐Rahman, BA Kozel, HH Zimmerman, Ulrich Broeckel, EV Semina

    出版 2013
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  8. 8
    Prevalence of left ventricular diastolic dysfunction in the community Results from a Doppler echocardiographic-based survey of a population sample

    Prevalence of left ventricular diastolic dysfunction in the community Results from a Doppler echocardiographic-based survey of a population sample 由 Marcus Fischer, Andrea Baessler, Hense Hw, Christian Hengstenberg, M Muscholl, Stephan Holmer, Angela Döring, Ulrich Broeckel, G. Riegger, Heribert Schunkert

    出版 2003
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  9. 9
    RNA Expression Profiling of Human iPSC-Derived Cardiomyocytes in a Cardiac Hypertrophy Model

    RNA Expression Profiling of Human iPSC-Derived Cardiomyocytes in a Cardiac Hypertrophy Model 由 Praful Aggarwal, Amy Turner, Andrea Matter, Steven Kattman, Alexander J. Stoddard, Rachel Lorier, Bradley Jay Swanson, Donna K. Arnett, Ulrich Broeckel

    出版 2014
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  10. 10
    Lack of Association Between a Polymorphism of the Aldosterone Synthase Gene and Left Ventricular Structure

    Lack of Association Between a Polymorphism of the Aldosterone Synthase Gene and Left Ventricular Structure 由 Heribert Schunkert, Christian Hengstenberg, Stephan Holmer, Ulrich Broeckel, Andreas Luchner, M Muscholl, Susanne Kürzinger, Angela Döring, Hans‐Werner Hense, Günter A.J. Riegger

    出版 1999
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  11. 11
    Distinct Heritable Patterns of Angiographic Coronary Artery Disease in Families With Myocardial Infarction

    Distinct Heritable Patterns of Angiographic Coronary Artery Disease in Families With Myocardial Infarction 由 Marcus Fischer, Ulrich Broeckel, Stephan Holmer, Andrea Baessler, Christian Hengstenberg, Bjoern Mayer, Jeanette Erdmann, G. Klein, G. Riegger, Howard J. Jacob, Heribert Schunkert

    出版 2005
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  12. 12
    Comparative Phenotypic and CARD15 Mutational Analysis Among African American, Hispanic, and White Children with Crohnʼs Disease

    Comparative Phenotypic and CARD15 Mutational Analysis Among African American, Hispanic, and White Children with Crohnʼs Disease 由 Subra Kugathasan, Anthony M. Loizides, Umesh Babusukumar, Erin McGuire, Tao Wang, Pleasant Hooper, Justin Nebel, Galina Kofman, Richard J. Noel, Ulrich Broeckel, Vasundhara Tolia

    出版 2005
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  13. 13
    Localization of a Small Genomic Region Associated with Elevated ACE

    Localization of a Small Genomic Region Associated with Elevated ACE 由 Xiaofeng Zhu, Colin A. McKenzie, Terrence Forrester, Deborah A. Nickerson, Ulrich Broeckel, Heribert Schunkert, Angela Doering, Howard J. Jacob, Stephen S. Rich, Mark J. Rieder

    出版 2000
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  14. 14
    Updated <i>DPYD</i><scp>HapB3</scp> haplotype structure and implications for pharmacogenomic testing

    Updated <i>DPYD</i><scp>HapB3</scp> haplotype structure and implications for pharmacogenomic testing 由 Amy Turner, Cyrine E. Haidar, Wenjian Yang, Erin C. Boone, Steven M. Offer, Philip E. Empey, Andrew Haddad, Saba Tahir, Gunter Scharer, Ulrich Broeckel, Andrea Gaedigk

    出版 2023
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  15. 15
    Preemptive Clinical Pharmacogenetics Implementation: Current Programs in Five US Medical Centers

    Preemptive Clinical Pharmacogenetics Implementation: Current Programs in Five US Medical Centers 由 Henry M. Dunnenberger, Kristine R. Crews, James M. Hoffman, Kelly E. Caudle, Ulrich Broeckel, Scott C. Howard, Robert J. Hunkler, Teri E. Klein, William E. Evans, Mary V. Relling

    出版 2014
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  16. 16
    Age‐ and Genotype‐Dependent Variability in the Protein Abundance and Activity of Six Major Uridine Diphosphate‐Glucuronosyltransferases in Human Liver

    Age‐ and Genotype‐Dependent Variability in the Protein Abundance and Activity of Six Major Uridine Diphosphate‐Glucuronosyltransferases in Human Liver 由 Deepak Kumar Bhatt, Aanchal Mehrotra, Andrea Gaedigk, Revathi Chapa, Abdul Basit, Haeyoung Zhang, Prachi Choudhari, Mikael Boberg, Robin E. Pearce, Roger Gaedigk, Ulrich Broeckel, J. Steven Leeder, Bhagwat Prasad

    出版 2018
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  17. 17
    Characterization of Reference Materials for Genetic Testing of CYP2D6 Alleles

    Characterization of Reference Materials for Genetic Testing of CYP2D6 Alleles 由 Andrea Gaedigk, Amy Turner, Robin E. Everts, Stuart A. Scott, Praful Aggarwal, Ulrich Broeckel, Gwendolyn A. McMillin, Roberta Melis, Erin C. Boone, Victoria M. Pratt, Lisa V. Kalman

    出版 2019
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  18. 18
    PITX2 and FOXC1 spectrum of mutations in ocular syndromes

    PITX2 and FOXC1 spectrum of mutations in ocular syndromes 由 Linda M. Reis, Rebecca C. Tyler, Bethany A. Kloss, Kala F. Schilter, Alex V. Levin, R. Brian Lowry, Petra Zwijnenburg, Eliza Stroh, Ulrich Broeckel, Jeffrey C. Murray, Elena V. Semina

    出版 2012
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  19. 19
    Loss-of-function thrombospondin-1 mutations in familial pulmonary hypertension

    Loss-of-function thrombospondin-1 mutations in familial pulmonary hypertension 由 James P. Maloney, Robert S. Stearman, Todd Bull, David W. Calabrese, Megan L. Tripp-Addison, Marilee J. Wick, Ulrich Broeckel, Ivan M. Robbins, Lisa Wheeler, Joy D. Cogan, James E. Loyd

    出版 2011
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  20. 20
    PLCγ-dependent mTOR signalling controls IL-7-mediated early B cell development

    PLCγ-dependent mTOR signalling controls IL-7-mediated early B cell development 由 Mei Yu, Yuhong Chen, Hu Zeng, Yongwei Zheng, Guoping Fu, Wen Zhu, Ulrich Broeckel, Praful Aggarwal, Amy Turner, Geoffrey Neale, Cliff Guy, Nan Zhu, Hongbo Chi, Renren Wen, Demin Wang

    出版 2017
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