Autosomal recessive osteopetrosis (ARO) is a genetic bone disease that can be caused by mutations in the CLCN7 gene preventing osteoclast-mediated bone resorption. We generated a human induced pluripotent stem cell (hiPSC) line, BIHi002-A, from peripheral blood mononuclear cells of an ARO patient carrying the CLCN7 mutations c.875G>A and c.1208G>A using Sendai viral vectors. The pluripotent identity of the BIHi002-A line was confirmed by their expression of typical markers for undifferentiated hiPSCs, their capacity to differentiate into cells of the three germ layers and by PluriTest analysis. The BIHi002-A line provides a tool for disease modelling and therapy development
Hypomyelinating Leukodystrophy 22 (HLD22) is caused by a stoploss mutation in CLDN11. To study the m...
Fibrodysplasia ossificans progressiva (FOP) is a rare autosomal dominant disorder of progressive oss...
We report the generation of human induced pluripotent stem cells (hiPSCs) from dermal fibroblasts of...
Pathogenic sequence variants in the Sorting Nexin 10 (SNX10) gene have been associated with autosoma...
Autosomal recessive osteopetrosis (ARO) is a rare inherited disorder leading to increased bone densi...
Autosomal recessive osteopetrosis is a human bone disease mainly caused by TCIRG1 gene mutations tha...
BACKGROUND: Infantile malignant osteopetrosis (IMO) is an autosomal recessive disorder characterized...
We generated human induced pluripotent stem cells (hiPSCs) from dermal fibroblasts of a 40 years old...
Die autosomal-rezessive Osteopetrose (ARO) ist eine schwere, erblich bedingte Knochenerkrankung, die...
More than 500 rare genetic bone disorders have been described, but for many of them only limited tre...
More than 500 rare genetic bone disorders have been described, but for many of them only limited tre...
Background Autosomal recessive osteopetrosis is a genetically and phenotypically heterogeneous disea...
Human recessive osteopetrosis (ARO) represents a group of diseases in which, due to a defect in oste...
The human induced pluripotent stem cell (hiPSC) line RP1-FiPS4F1 generated from the patient with aut...
Autosomal recessive osteopetrosis is a human bone disease mainly caused by TCIRG1 gene mutations tha...
Hypomyelinating Leukodystrophy 22 (HLD22) is caused by a stoploss mutation in CLDN11. To study the m...
Fibrodysplasia ossificans progressiva (FOP) is a rare autosomal dominant disorder of progressive oss...
We report the generation of human induced pluripotent stem cells (hiPSCs) from dermal fibroblasts of...
Pathogenic sequence variants in the Sorting Nexin 10 (SNX10) gene have been associated with autosoma...
Autosomal recessive osteopetrosis (ARO) is a rare inherited disorder leading to increased bone densi...
Autosomal recessive osteopetrosis is a human bone disease mainly caused by TCIRG1 gene mutations tha...
BACKGROUND: Infantile malignant osteopetrosis (IMO) is an autosomal recessive disorder characterized...
We generated human induced pluripotent stem cells (hiPSCs) from dermal fibroblasts of a 40 years old...
Die autosomal-rezessive Osteopetrose (ARO) ist eine schwere, erblich bedingte Knochenerkrankung, die...
More than 500 rare genetic bone disorders have been described, but for many of them only limited tre...
More than 500 rare genetic bone disorders have been described, but for many of them only limited tre...
Background Autosomal recessive osteopetrosis is a genetically and phenotypically heterogeneous disea...
Human recessive osteopetrosis (ARO) represents a group of diseases in which, due to a defect in oste...
The human induced pluripotent stem cell (hiPSC) line RP1-FiPS4F1 generated from the patient with aut...
Autosomal recessive osteopetrosis is a human bone disease mainly caused by TCIRG1 gene mutations tha...
Hypomyelinating Leukodystrophy 22 (HLD22) is caused by a stoploss mutation in CLDN11. To study the m...
Fibrodysplasia ossificans progressiva (FOP) is a rare autosomal dominant disorder of progressive oss...
We report the generation of human induced pluripotent stem cells (hiPSCs) from dermal fibroblasts of...