International audienceAbstract Pathogenic variants in the gene encoding the small GTPase Ras analogue in Brain 39b (RAB39B) are associated with early-onset parkinsonism. In this study we investigated the expression and localization of RAB39B (RNA and protein) in mouse brain tissue to gain a better understanding of its normal physiological function(s) and role in disease. We developed novel resources, including monoclonal antibodies directed against RAB39B and mice with Rab39b knockout, and performed real-time PCR and western blot analysis on whole brain lysates. To determine the spatial localization of Rab39b RNA and protein, we performed in-situ hybridization and immunohistochemistry on fresh frozen and fixed brain tissue. Our results show...
Rhes is one of the most interesting genes regulated by thyroid hormones that, through the inhibition...
Objective: Determine Rab GTPase expression changes in α-synucleinopathy and tauopathy disorders. B...
Abstract Hexanucleotide repeat expansion in C9orf72 is the most common genetic cause of frontotempor...
Pathogenic variants in the gene encoding the small GTPase Ras analogue in Brain 39b (RAB39B) are ass...
© 2018 Dr Yujing GaoLoss of function mutations in Ras analog in brain 39B (RAB39B) can cause Parkins...
Loss of function mutations within the vesicular trafficking protein Ras analogy in brain 39B (RAB39B...
Loss of function mutations within the vesicular trafficking protein Ras analogy in brain 39B (RAB39B...
Abstract Autosomal dominant pathogenic mutations in Leucine-rich repeat kinase 2 (LRRK2) cause Parki...
Advances in understanding the etiology of Parkinson disease have been driven by the identification o...
In patients affected by Parkinson’s disease (PD), the most common neurodegenerative movement disorde...
Intracellular vesicular trafficking is essential for neuronal development, function, and homeostasis...
Parkinson’s disease (PD) is the second most frequent neurodegenerative disease. It is characterized ...
Intracellular vesicular trafficking is essential for neuronal development, function, and homeostasis...
Advances in understanding the etiology of Parkinson disease have been driven by the identification o...
International audienceRab proteins are small molecular weight guanosine triphosphatases involved in ...
Rhes is one of the most interesting genes regulated by thyroid hormones that, through the inhibition...
Objective: Determine Rab GTPase expression changes in α-synucleinopathy and tauopathy disorders. B...
Abstract Hexanucleotide repeat expansion in C9orf72 is the most common genetic cause of frontotempor...
Pathogenic variants in the gene encoding the small GTPase Ras analogue in Brain 39b (RAB39B) are ass...
© 2018 Dr Yujing GaoLoss of function mutations in Ras analog in brain 39B (RAB39B) can cause Parkins...
Loss of function mutations within the vesicular trafficking protein Ras analogy in brain 39B (RAB39B...
Loss of function mutations within the vesicular trafficking protein Ras analogy in brain 39B (RAB39B...
Abstract Autosomal dominant pathogenic mutations in Leucine-rich repeat kinase 2 (LRRK2) cause Parki...
Advances in understanding the etiology of Parkinson disease have been driven by the identification o...
In patients affected by Parkinson’s disease (PD), the most common neurodegenerative movement disorde...
Intracellular vesicular trafficking is essential for neuronal development, function, and homeostasis...
Parkinson’s disease (PD) is the second most frequent neurodegenerative disease. It is characterized ...
Intracellular vesicular trafficking is essential for neuronal development, function, and homeostasis...
Advances in understanding the etiology of Parkinson disease have been driven by the identification o...
International audienceRab proteins are small molecular weight guanosine triphosphatases involved in ...
Rhes is one of the most interesting genes regulated by thyroid hormones that, through the inhibition...
Objective: Determine Rab GTPase expression changes in α-synucleinopathy and tauopathy disorders. B...
Abstract Hexanucleotide repeat expansion in C9orf72 is the most common genetic cause of frontotempor...