Articles with "rab39b" as a keyword



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RAB39B Deficiency Impairs Learning and Memory Partially Through Compromising Autophagy

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Published in 2020 at "Frontiers in Cell and Developmental Biology"

DOI: 10.3389/fcell.2020.598622

Abstract: RAB39B is located on the X chromosome and encodes the RAB39B protein that belongs to the RAB family. Mutations in RAB39B are known to be associated with X-linked intellectual disability (XLID), Parkinson’s disease, and autism.… read more here.

Keywords: deficiency impairs; rab39b deficiency; rab39b; learning memory ... See more keywords
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Loss of RAB39B does not alter MPTP-induced Parkinson’s disease-like phenotypes in mice

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Published in 2023 at "Frontiers in Aging Neuroscience"

DOI: 10.3389/fnagi.2023.1087823

Abstract: Parkinson’s disease (PD) is a common neurodegenerative movement disorder with undetermined etiology. A major pathological hallmark of PD is the progressive degeneration of dopaminergic neurons in the substantia nigra. Loss-of-function mutations in the RAB39B gene,… read more here.

Keywords: mptp induced; parkinson disease; loss; rab39b ... See more keywords
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RAB39B as a Chemosensitivity-Related Biomarker for Diffuse Large B-Cell Lymphoma

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Published in 2022 at "Frontiers in Pharmacology"

DOI: 10.3389/fphar.2022.931501

Abstract: Background: Diffuse large B-cell lymphoma (DLBCL) is the most common aggressive lymphoma with an increased tendency to relapse or refractoriness. RAB39B, a member of the Ras-oncogene superfamily, is associated with a variety of tumors. Nevertheless,… read more here.

Keywords: cell; lymphoma; dlbcl; rab39b expression ... See more keywords