Parkinson's disease is a common neurogenetic degenerative disease that can be caused by a variety of genetic mutations. RAB39B gene mutations have recently been identified as a cause of Parkinson's disease. We collected skin tissue samples from a family with mutations in RAB39B for our clinical study. Additionally, we constructed patient-derived induced pluripotent stem cells (iPSCs) from the patient’s uncle using an unintegrated reprogramming plasmid transfection method to create a reliable cell model for the subsequent study of Parkinson's disease
Leucine rich repeat kinase (LRRK2) is the most prevalent genetic cause for Parkinson's disease. LRRK...
An induced pluripotent stem cell (iPSC) line was generated from a 36-year-old patient with sporadic ...
Mutations in RAB39B are a known cause of X-linked early onset Parkinson's disease. Isogenic human em...
Ras-related protein 39B (RAB39B) mutation has been reported as a potential cause of X-linked Parkins...
Mutations in the glucocerebrosidase (GBA) gene have been associated with the development of Parkinso...
The leucine-rich repeat kinase 2 (LRRK2) p.G2019S mutation is the most common genetic cause of Parki...
Parkinson's disease (PD) is a neurodegenerative disease with unknown etiology. Here we show the gene...
Mutations in the PARK2 gene, which encodes PARKIN, are the most frequent cause of autosomal recessiv...
Fibroblasts were obtained from a 76 year-old man diagnosed with Parkinson's disease (PD). The diseas...
Mutations in the PARK2 gene, which encodes PARKIN, are the most frequent cause of autosomal recessiv...
We generated a human induced pluripotent stem cell (iPSC) line from the skin fibroblasts of a 62-yea...
Skin fibroblasts were collected from a 44-year-old patient with sporadic case of Parkinson's disease...
Here, we describe the generation of an induced pluripotent stem cell (iPSC) line, from a male patien...
Mutations in PINK1 and Parkin are two of the main causes of recessive early-onset Parkinson’s diseas...
Mutations in RAB39B are a known cause of X-linked early onset Parkinson\u27s disease. Isogenic human...
Leucine rich repeat kinase (LRRK2) is the most prevalent genetic cause for Parkinson's disease. LRRK...
An induced pluripotent stem cell (iPSC) line was generated from a 36-year-old patient with sporadic ...
Mutations in RAB39B are a known cause of X-linked early onset Parkinson's disease. Isogenic human em...
Ras-related protein 39B (RAB39B) mutation has been reported as a potential cause of X-linked Parkins...
Mutations in the glucocerebrosidase (GBA) gene have been associated with the development of Parkinso...
The leucine-rich repeat kinase 2 (LRRK2) p.G2019S mutation is the most common genetic cause of Parki...
Parkinson's disease (PD) is a neurodegenerative disease with unknown etiology. Here we show the gene...
Mutations in the PARK2 gene, which encodes PARKIN, are the most frequent cause of autosomal recessiv...
Fibroblasts were obtained from a 76 year-old man diagnosed with Parkinson's disease (PD). The diseas...
Mutations in the PARK2 gene, which encodes PARKIN, are the most frequent cause of autosomal recessiv...
We generated a human induced pluripotent stem cell (iPSC) line from the skin fibroblasts of a 62-yea...
Skin fibroblasts were collected from a 44-year-old patient with sporadic case of Parkinson's disease...
Here, we describe the generation of an induced pluripotent stem cell (iPSC) line, from a male patien...
Mutations in PINK1 and Parkin are two of the main causes of recessive early-onset Parkinson’s diseas...
Mutations in RAB39B are a known cause of X-linked early onset Parkinson\u27s disease. Isogenic human...
Leucine rich repeat kinase (LRRK2) is the most prevalent genetic cause for Parkinson's disease. LRRK...
An induced pluripotent stem cell (iPSC) line was generated from a 36-year-old patient with sporadic ...
Mutations in RAB39B are a known cause of X-linked early onset Parkinson's disease. Isogenic human em...