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Journal of Inherited Metabolic Disease|July 8, 2018
Induced pluripotent stem cells (iPSCs) as model to study inherited defects of neurotransmission in inborn errors of metabolismSabine Jung-Klawitter, Thomas Opladen
Cells|August 14, 2019
Analysis of Catecholamines and Pterins in Inborn Errors of Monoamine Neurotransmitter Metabolism-From Past to FutureSabine Jung-Klawitter, Oya Kuseyri Hübschmann
Neuropediatrics|October 30, 2018
Inherited Disorders of Neurotransmitters: Classification and Practical Approaches for Diagnosis and TreatmentHeiko Brennenstuhl, Sabine Jung-Klawitter, Birgit Assmann, et al.
Stem Cell Research|April 12, 2017
Generation of an iPSC line from a patient with GTP cyclohydrolase 1 (GCH1) deficiency: HDMC0061i-GCH1Sabine Jung-Klawitter, Juliane Ebersold, Gudrun Göhring, et al.
Stem Cell Research|September 17, 2025
iPSC line DHMCi019-A is generated from a patient with hereditary nephrotic syndrome harboring compound heterozygous NPHS2 variantsMansoureh Tabatabaeifar, Robert Matthes, Karin Burau, et al.
Stem Cell Research|September 20, 2025
iPSC line DHMCi010-A is derived from a hereditary nephrotic syndrome patient with an autosomal recessive NPHS2 mutationRobert Matthes, Mansoureh Tabatabaeifar, Karin Burau, et al.
Stem Cell Research|March 23, 2019
Generation of 2 iPSC clones from a patient with DNAJC12 deficiency: DHMCi003-A and DHMCi003-BSabine Jung-Klawitter, Selina Wächter, Maike Hagedorn, et al.
Stem Cell Research|December 10, 2016
Generation of an iPSC line from a patient with tyrosine hydroxylase (TH) deficiency: TH-1 iPSCSabine Jung-Klawitter, Nenad Blau, Attila Sebe, et al.
Stem Cell Research|October 23, 2021
Generation of an induced pluripotent stem cell line (DHMCi007-A) from a patient with autosomal recessive polycystic kidney disease (ARPKD) carrying a homozygous missense mutation in the fibrocystin-encoding PKHD1 geneMansoureh Tabatabaeifar, Theresa Leonie Fluhr, Hanna Syring, et al.
Stem Cell Research|October 25, 2021
Generation of an induced pluripotent stem cell line (DHMCi006-A) from a patient with autosomal recessive polycystic kidney disease (ARPKD) carrying a compound heterozygous missense mutation in the fibrocystin encoding PKHD1 geneTheresa Leonie Fluhr, Mansoureh Tabatabaeifar, Hanna Syring, et al.
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