The ASS1 gene encodes argininosuccinate synthetase-1, a cytosolic enzyme with a critical role in the urea cycle. Mutations are found in all ASS1 exons and cause the autosomal recessive disorder citrullinemia. Using CRISPR/Cas9-editing, we established the WAe001-A-13 cell line, which was heterozygous for an ASS1 mutation, from the human embryonic stem cell line H1. The WAe001-A-13 cell line maintained the pluripotent phenotype, the ability to differentiate into all three germ layers and a normal karyotype
Since the first reported generation of induced pluripotent stem cells (hiPSCs) from human somatic ce...
Arrhythmogenic Cardiomyopathy (ACM) is a rare genetic cardiac disease predominantly associated with ...
AbstractThe gene of ATP-binding cassette subfamily C member 8 (Abcc8) is cytogenetically located at ...
Urea cycle disorders are incurable enzymopathies that affect nitrogen metabolism and typically lead ...
Urea cycle disorders are incurable enzymopathies that affect nitrogen metabolism and typically lead ...
Glycogen debranching enzyme (GDE) plays a critical role in glycogenolysis. Mutations in the GDE gene...
p53 is a tumor suppressor gene involved mainly in the regulation of the G1/S cell cycle phase, DNA r...
Here, we generated a monoallelic mutation in the TLE3 (Transducin Like Enhancer of Split 3) gene usi...
Abstract: As one of the most essential genome guardians, p53 and its mutants have been suggested ass...
Fibroblasts isolated from a skin biopsy of a healthy 46-year-old female were infected with Sendai vi...
The human GLI3 protein has a dual function as a transcriptional activator or repressor of hedgehog s...
GNB5 loss-of-function pathogenic variants cause IDDCA, a rare autosomal recessive human genetic dise...
The human SMO protein encoded by the smoothened (SMO) gene acts as a positive mediator for Hedgehog ...
AbstractHere, we generated a monoallelic mutation in the TLE3 (Transducin Like Enhancer of Split 3) ...
The human induced pluripotent stem cell (hiPSC) line RP1-FiPS4F1 generated from the patient with aut...
Since the first reported generation of induced pluripotent stem cells (hiPSCs) from human somatic ce...
Arrhythmogenic Cardiomyopathy (ACM) is a rare genetic cardiac disease predominantly associated with ...
AbstractThe gene of ATP-binding cassette subfamily C member 8 (Abcc8) is cytogenetically located at ...
Urea cycle disorders are incurable enzymopathies that affect nitrogen metabolism and typically lead ...
Urea cycle disorders are incurable enzymopathies that affect nitrogen metabolism and typically lead ...
Glycogen debranching enzyme (GDE) plays a critical role in glycogenolysis. Mutations in the GDE gene...
p53 is a tumor suppressor gene involved mainly in the regulation of the G1/S cell cycle phase, DNA r...
Here, we generated a monoallelic mutation in the TLE3 (Transducin Like Enhancer of Split 3) gene usi...
Abstract: As one of the most essential genome guardians, p53 and its mutants have been suggested ass...
Fibroblasts isolated from a skin biopsy of a healthy 46-year-old female were infected with Sendai vi...
The human GLI3 protein has a dual function as a transcriptional activator or repressor of hedgehog s...
GNB5 loss-of-function pathogenic variants cause IDDCA, a rare autosomal recessive human genetic dise...
The human SMO protein encoded by the smoothened (SMO) gene acts as a positive mediator for Hedgehog ...
AbstractHere, we generated a monoallelic mutation in the TLE3 (Transducin Like Enhancer of Split 3) ...
The human induced pluripotent stem cell (hiPSC) line RP1-FiPS4F1 generated from the patient with aut...
Since the first reported generation of induced pluripotent stem cells (hiPSCs) from human somatic ce...
Arrhythmogenic Cardiomyopathy (ACM) is a rare genetic cardiac disease predominantly associated with ...
AbstractThe gene of ATP-binding cassette subfamily C member 8 (Abcc8) is cytogenetically located at ...