Search Results - Oexle, Konrad
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Phenotypic and genome-wide studies on dicarbonyls: major associations to glomerular filtration rate and gamma-glutamyltransferase activity by Harrer, Philip (Author) , Inderhees, Julica (Author) , Zhao, Chen (Author) , Schormair, Barbara (Author) , Tilch, Erik (Author) , Gieger, Christian (Author) , Peters, Annette (Author) , Jöhren, Olaf (Author) , Fleming, Thomas (Author) , Nawroth, Peter Paul (Author) , Berger, Klaus (Author) , Hermesdorf, Marco (Author) , Winkelmann, Juliane (Author) , Schwaninger, Markus (Author) , Oexle, Konrad (Author) ,
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The reactive pyruvate metabolite dimethylglyoxal mediates neurological consequences of diabetes by Rhein, Sina (Author) , Costalunga, Riccardo (Author) , Inderhees, Julica (Author) , Gürtzgen, Tammo (Author) , Faupel, Teresa Christina (Author) , Shaheryar, Zaib (Author) , Arrulo Pereira, Adriana (Author) , Othman, Alaa (Author) , Begemann, Kimberly (Author) , Binder, Sonja (Author) , Stölting, Ines (Author) , Dorta, Valentina (Author) , Nawroth, Peter Paul (Author) , Fleming, Thomas (Author) , Oexle, Konrad (Author) , Prevot, Vincent (Author) , Nogueiras, Ruben (Author) , Meyhöfer, Svenja (Author) , Meyhöfer, Sebastian M. (Author) , Schwaninger, Markus (Author) ,
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3.7 Mb tandem microduplication in chromosome 5p13.1-p13.2 associated with developmental delay, macrocephaly, obesity, and lymphedema: further characterization of the dup(5p13) synd... by Oexle, Konrad (Author) , Hempel, Maja (Author) , Jauch, Anna (Author) , Meitinger, Thomas (Author) , Rivera-Brugués, Núria (Author) , Stengel-Rutkowski, Sabine (Author) , Strom, Tim (Author) ,
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Related Subjects
Autism
Blood-brain barrier
Cerebrovascular disorders
Diabetes complications
Dicarbonyl compounds
Dietary carbohydrates
Dup(5p) syndrome
Genome-wide association study
Glucose
Kidney function
Liver enzymes
Low posterior hairline
Lymphedema
Mental retardation
Molecular medicine
Obesity
Phenotypic association study