Fibroblasts from a female patient carrying a heterozygous variation in GTP cyclohydrolase 1 (GCH1; OMIM: 600225; HGNC: 4193; c.235_240del/p.(L79_S80del)), the rate-limiting enzyme of tetrahydrobiopterin (BH4) synthesis, were reprogrammed to iPSCs using the Cytotune®-iPS 2.0 Sendai Reprogramming Kit (Invitrogen) delivering the four reprogramming factors Oct3/4, Sox2, c-Myc and Klf4. Pluripotency of HDMC0061i-GCH1 was verified using immunohistochemistry and RT-PCR analysis. Cells differentiated spontaneously into the 3 germ layers in vitro and presented a normal karyotype. HDMC0061i-GCH1 represents the first model system to elucidate the pathomechanism underlying this rare metabolic disease and a useful tool for drug testing
AbstractWe generated an induced pluripotent stem cell (iPSC) line from a Bernard–Soulier Syndrome (B...
Skin fibroblasts were isolated from a male patient with DNAJC12 deficiency and reprogrammed to iPSCs...
Human iPSC line TSD-01-hiPSC was generated from fibroblasts of a patient with infantile Tay-Sachs di...
Fibroblasts from a female patient carrying a heterozygous variation in GTP cyclohydrolase 1 (GCH1; O...
Fibroblasts from a male patient with compound heterozygous variants in the tyrosine hydroxylase gene...
AbstractFibroblasts from a male patient with compound heterozygous variants in the tyrosine hydroxyl...
AbstractIntroductionGTP cyclohydrolase I (GTPCH) catalyses the first and rate-limiting reaction in t...
INTRODUCTION: GTP cyclohydrolase I (GTPCH) catalyses the first and rate-limiting reaction in the syn...
The hph-1 ENU-mutant mouse provides a model of tetrahydrobiopterin deficiency for studying hyperphen...
Fibroblasts of a patient with Infantile Liver Failure Syndrome 2 (OMIM #616483) due to a homozygous ...
GTP cyclohydrolase I is the first and rate-limiting enzyme for the biosynthesis of tetrahydrobiopter...
Click on the DOI link to access the article (may not be free).GTP cyclohydrolase I catalyzes the ini...
Mucopolysaccharidosis type I-Hurler (MPS1-H) is the most severe form of inherited metabolic diseases...
Primary Hyperoxaluria Type I (PH1) is a rare autosomal recessive metabolic disorder characterized by...
The human iPSC cell line, GLC-FiPS4F1 (ESi047-A), derived from dermal fibroblast from the patient wi...
AbstractWe generated an induced pluripotent stem cell (iPSC) line from a Bernard–Soulier Syndrome (B...
Skin fibroblasts were isolated from a male patient with DNAJC12 deficiency and reprogrammed to iPSCs...
Human iPSC line TSD-01-hiPSC was generated from fibroblasts of a patient with infantile Tay-Sachs di...
Fibroblasts from a female patient carrying a heterozygous variation in GTP cyclohydrolase 1 (GCH1; O...
Fibroblasts from a male patient with compound heterozygous variants in the tyrosine hydroxylase gene...
AbstractFibroblasts from a male patient with compound heterozygous variants in the tyrosine hydroxyl...
AbstractIntroductionGTP cyclohydrolase I (GTPCH) catalyses the first and rate-limiting reaction in t...
INTRODUCTION: GTP cyclohydrolase I (GTPCH) catalyses the first and rate-limiting reaction in the syn...
The hph-1 ENU-mutant mouse provides a model of tetrahydrobiopterin deficiency for studying hyperphen...
Fibroblasts of a patient with Infantile Liver Failure Syndrome 2 (OMIM #616483) due to a homozygous ...
GTP cyclohydrolase I is the first and rate-limiting enzyme for the biosynthesis of tetrahydrobiopter...
Click on the DOI link to access the article (may not be free).GTP cyclohydrolase I catalyzes the ini...
Mucopolysaccharidosis type I-Hurler (MPS1-H) is the most severe form of inherited metabolic diseases...
Primary Hyperoxaluria Type I (PH1) is a rare autosomal recessive metabolic disorder characterized by...
The human iPSC cell line, GLC-FiPS4F1 (ESi047-A), derived from dermal fibroblast from the patient wi...
AbstractWe generated an induced pluripotent stem cell (iPSC) line from a Bernard–Soulier Syndrome (B...
Skin fibroblasts were isolated from a male patient with DNAJC12 deficiency and reprogrammed to iPSCs...
Human iPSC line TSD-01-hiPSC was generated from fibroblasts of a patient with infantile Tay-Sachs di...