Jansen, Alexander C.
616  Ergebnisse:
Personensuche X
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4

Heterogeneous clinical phenotypes and cerebral malformation..:

Vandervore, Laura V ; Schot, Rachel ; Kasteleijn, Esmee...
https://research.rug.nl/en/publications/00b35166-d08e-4bbb-a3f7-1a54850d4541.  , 2019
 
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7

Structural Variations in Chlorosomes from Wild-Type and a b..:

Guenther, Lisa M ; Loehner, Alexander ; Reiher, Carolin...
https://research.rug.nl/en/publications/70035ed1-93cd-4394-beb5-b7c5ec3e069d.  , 2018
 
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8

CCDC115 Deficiency Causes a Disorder of Golgi Homeostasis w..:

Jansen, Jos C ; Cirak, Sebahattin ; van Scherpenzeel, Monique...
Jansen , J C , Cirak , S , van Scherpenzeel , M , Timal , S , Reunert , J , Rust , S , Perez , B , Vicogne , D , Krawitz , P , Wada , Y , Ashikov , A , Perez-Cerda , C , Medrano , C , Arnoldy , A , Hoischen , A , Huijben , K , Steenbergen , G , Quelhas , D , Diogo , L , Rymen , D , Jaeken , J , Guffon , N , Cheillan , D , van den Heuvel , L P , Maeda , Y , Kaiser , O , Schara , U , Gerner , P , van den Boogert , M A W , Holleboom , A G , Nassogne , M-C , Sokal , E , Salomon , J , van den Bogaart , G , Drenth , J P H , Huynen , M A , Veltman , J A , Wevers , R A , Morava , E , Matthijs , G , Foulquier , F , Marquardt , T & Lefeber , D J 2016 , ' CCDC115 Deficiency Causes a Disorder of Golgi Homeostasis with Abnormal Protein Glycosylation ' , American Journal of Human Genetics , vol. 98 , no. 2 , pp. 310-321 . https://doi.org/10.1016/j.ajhg.2015.12.010.  , 2016
 
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9

TMEM199 Deficiency Is a Disorder of Golgi Homeostasis Chara..:

Jansen, Jos C ; Timal, Sharita ; van Scherpenzeel, Monique...
Jansen , J C , Timal , S , van Scherpenzeel , M , Michelakakis , H , Vicogne , D , Ashikov , A , Moraitou , M , Hoischen , A , Huijben , K , Steenbergen , G , van den Boogert , M A W , Porta , F , Calvo , P L , Mavrikou , M , Cenacchi , G , van den Bogaart , G , Salomon , J , Holleboom , A G , Rodenburg , R J , Drenth , J P H , Huynen , M A , Wevers , R A , Morava , E , Foulquier , F , Veltman , J A & Lefeber , D J 2016 , ' TMEM199 Deficiency Is a Disorder of Golgi Homeostasis Characterized by Elevated Aminotransferases, Alkaline Phosphatase, and Cholesterol and Abnormal Glycosylation ' , American Journal of Human Genetics , vol. 98 , no. 2 , pp. 322-330 . https://doi.org/10.1016/j.ajhg.2015.12.011.  , 2016
 
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Systematic identification of trans eQTLs as putative driver..:

Westra, Harm-Jan ; Peters, Marjolein J ; Esko, Tonu...
https://research.rug.nl/en/publications/9be58926-f59b-4b9a-9abc-0296fe6595e4.  , 2013
 
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13

The dynamic architecture of the metabolic switch in Strepto..:

Nieselt, Kay ; Battke, Florian ; Herbig, Alexander...
https://research.rug.nl/en/publications/46541ca5-e4a5-47cf-981d-3c92484bd94b.  , 2010
 
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