Skin fibroblasts were isolated from a male patient with DNAJC12 deficiency and reprogrammed to iPSCs using the Cytotune®-iPS 2.0 Sendai Reprogramming Kit (Invitrogen). Two clones, DHMCi003-A and DHMCi003-B, were characterized for expression of pluripotency marker genes (Oct4, Nanog, Lin28, SSEA-4, TRA-1-60) and differentiated into all three germ layers using embryoid body (EB) formation. Karyotype of both clones was normal and presence of the homozygous mutation in the DNAJC12 gene was verified by PCR and Sanger sequencing. Both clones represent a useful tool to study the pathomechanisms underlying the deficiency
Peripheral blood was collected from a 7-year-old male patient with an X-linked recessive mutation of...
Heterozygous variants in the KCNQ3 gene cause epileptic and/or developmental disorders of varying se...
We produced an iPSC line from a patient with Joubert syndrome carrying the homozygous c.787dupC vari...
Fibroblasts of a patient with Infantile Liver Failure Syndrome 2 (OMIM #616483) due to a homozygous ...
GNB5 loss-of-function pathogenic variants cause IDDCA, a rare autosomal recessive human genetic dise...
A human iPSC line was generated from exfoliated renal epithelial (ERE) cells of a patient affected w...
The INK4 locus is considered as a hot-spot region for the complex genetic disorders, including cance...
<p>A subset of iPSC clones were characterized for pluripotency. The experiments demonstrated in this...
Four human iPSC cell lines (one Jervell and Lange-Nielsen Syndrome, one Long QT Syndrome-type 1 and ...
We report the generation of three isogenic iPSC clones (UNIBSi007-A, UNIBSi007-B, and UNIBSi007-C) o...
Limb-girdle muscular dystrophies (LGMDs) are a large group of heterogenous genetic diseases characte...
We present generation of iPSCs from CD34+ cells isolated from peripheral blood, collected during aph...
We report the generation of human induced pluripotent stem cells (hiPSCs) from dermal fibroblasts of...
Skin fibroblasts from a patient with neurodevelopmental and speech delay, anxiety disorder, macrocep...
Fibroblasts from a female patient carrying a heterozygous variation in GTP cyclohydrolase 1 (GCH1; O...
Peripheral blood was collected from a 7-year-old male patient with an X-linked recessive mutation of...
Heterozygous variants in the KCNQ3 gene cause epileptic and/or developmental disorders of varying se...
We produced an iPSC line from a patient with Joubert syndrome carrying the homozygous c.787dupC vari...
Fibroblasts of a patient with Infantile Liver Failure Syndrome 2 (OMIM #616483) due to a homozygous ...
GNB5 loss-of-function pathogenic variants cause IDDCA, a rare autosomal recessive human genetic dise...
A human iPSC line was generated from exfoliated renal epithelial (ERE) cells of a patient affected w...
The INK4 locus is considered as a hot-spot region for the complex genetic disorders, including cance...
<p>A subset of iPSC clones were characterized for pluripotency. The experiments demonstrated in this...
Four human iPSC cell lines (one Jervell and Lange-Nielsen Syndrome, one Long QT Syndrome-type 1 and ...
We report the generation of three isogenic iPSC clones (UNIBSi007-A, UNIBSi007-B, and UNIBSi007-C) o...
Limb-girdle muscular dystrophies (LGMDs) are a large group of heterogenous genetic diseases characte...
We present generation of iPSCs from CD34+ cells isolated from peripheral blood, collected during aph...
We report the generation of human induced pluripotent stem cells (hiPSCs) from dermal fibroblasts of...
Skin fibroblasts from a patient with neurodevelopmental and speech delay, anxiety disorder, macrocep...
Fibroblasts from a female patient carrying a heterozygous variation in GTP cyclohydrolase 1 (GCH1; O...
Peripheral blood was collected from a 7-year-old male patient with an X-linked recessive mutation of...
Heterozygous variants in the KCNQ3 gene cause epileptic and/or developmental disorders of varying se...
We produced an iPSC line from a patient with Joubert syndrome carrying the homozygous c.787dupC vari...