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RAB39B encodes a member of the Rab family of proteins. Zusätzlich bieten wir Ihnen RAB39B Antikörper (42) und viele weitere Produktgruppen zu diesem Protein an.
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X-linked juvenile parkinsonism could be caused by a RAB39B mutation, and basal ganglia calcification may be a novel clinical feature of RAB39B-related parkinsonism.
RAB39B mutations are not a common cause of Parkinson's disease or dementia with Lewy bodies in Caucasian population
RAB39B mutations are not a common cause of early-onset or familial PD in our Taiwanese population.
RAB39B mutations are a rare finding in Parkinson disease patients
RAB39B is an essential regulator of vesicular-trafficking in clinically typical Parkinson's disease
RAB39B selectively regulates GluA2 (zeige GRIA2 Proteine) trafficking to determine synaptic AMPAR composition
The loss of RAB39B results in dysregulation of alpha-synuclein homeostasis and a spectrum of neuropathological features that implicate RAB39B in the pathogenesis of Parkinson disease and potentially other neurodegenerative disorders.
increased dosage of RAB39B causes a disturbed neuronal development leading to cognitive impairment
Data indicate that myosin Va (zeige MYO5A Proteine) interacted with multiple new Rab (zeige HRB Proteine) subfamilies including Rab6 (zeige RAB6A Proteine), Rab14 (zeige RAB14 Proteine) and Rab39B.
These results demonstrate developmental and functional neuronal alteration as a consequence of downregulation of RAB39B and emphasize the critical role of vesicular trafficking in the development of neurons and human intellectual abilities.
This gene encodes a member of the Rab family of proteins. Rab proteins are small GTPases that are involved in vesicular trafficking.
RAB39B, member RAS oncogene family
, ras-related protein Rab-39B-like
, ras-related protein Rab-39B