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Regulation of Endosomal Trafficking by Rab7 and Its Effectors in Neurons: Clues from Charcot-Marie-Tooth 2B Disease.
Mulligan RJ, Winckler B. Mulligan RJ, et al. Biomolecules. 2023 Sep 16;13(9):1399. doi: 10.3390/biom13091399. Biomolecules. 2023. PMID: 37759799 Free PMC article. Review.
The spatiotemporal regulation of endosomal receptor trafficking is particularly challenging in neurons because of their enormous size, their distinct intracellular domains with unique requirements (dendrites vs. axons), and their long lifespans as postmitotic, differentiated cell …
The spatiotemporal regulation of endosomal receptor trafficking is particularly challenging in neurons because of their enormous size, their …
Hereditary sensory neuropathies.
Houlden H, Blake J, Reilly MM. Houlden H, et al. Curr Opin Neurol. 2004 Oct;17(5):569-77. doi: 10.1097/00019052-200410000-00007. Curr Opin Neurol. 2004. PMID: 15367861 Review.
Certain forms of hereditary sensory and autonomic neuropathy, especially hereditary sensory and autonomic neuropathy type I, which has minimal autonomic involvement and is more accurately termed hereditary sensory neuropathy type I, can present in a very similar fas …
Certain forms of hereditary sensory and autonomic neuropathy, especially hereditary sensory and autonomic neuropathy type I, which ha …
Dynamin 2 in Charcot-Marie-Tooth disease.
Tanabe K, Takei K. Tanabe K, et al. Acta Med Okayama. 2012;66(3):183-90. doi: 10.18926/AMO/48557. Acta Med Okayama. 2012. PMID: 22729098 Free article. Review.
Charcot-Marie-Tooth disease (CMT) is an inherited neuronal disorder, and is induced by mutations of various genes associated with intracellular membrane traffic and cytoskeleton. A large GTPase, dynamin, which is known as a fission protein for endocyti
Charcot-Marie-Tooth disease (CMT) is an inherited neuronal disorder, and is induced by mutations of various gene
Charcot Marie Tooth 2B Peripheral Sensory Neuropathy: How Rab7 Mutations Impact NGF Signaling?
Liu H, Wu C. Liu H, et al. Int J Mol Sci. 2017 Feb 4;18(2):324. doi: 10.3390/ijms18020324. Int J Mol Sci. 2017. PMID: 28165391 Free PMC article. Review.
Charcot-Marie-Tooth 2B peripheral sensory neuropathy (CMT2B) is a debilitating autosomal dominant hereditary sensory neuropathy. ...We argue that better models (rodent animals and human neurons) of CMT2B are needed to precisely define the disease
Charcot-Marie-Tooth 2B peripheral sensory neuropathy (CMT2B) is a debilitating autosomal dominant hereditary sen
Rab7 may be a novel therapeutic target for neurologic diseases as a key regulator in autophagy.
Wen H, Zhan L, Chen S, Long L, Xu E. Wen H, et al. J Neurosci Res. 2017 Oct;95(10):1993-2004. doi: 10.1002/jnr.24034. Epub 2017 Feb 10. J Neurosci Res. 2017. PMID: 28186670 Review.
Rab7-mediated macroautophagy is closely associated with various pathological processes of several neurologic diseases, such as Parkinson's disease, Huntington's disease, Alzheimer's disease, Charcot-Marie-Tooth type 2B di
Rab7-mediated macroautophagy is closely associated with various pathological processes of several neurologic diseases, such as Parkinson's …
Rab7 and the CMT2B disease.
Cogli L, Piro F, Bucci C. Cogli L, et al. Biochem Soc Trans. 2009 Oct;37(Pt 5):1027-31. doi: 10.1042/BST0371027. Biochem Soc Trans. 2009. PMID: 19754445 Review.
The CMT2B (Charcot-Marie-Tooth type 2B) disease is an autosomal dominant axonal neuropathy. Sensory loss, distal muscle weakness and wasting, frequent foot ulcers and amputations of the toes due to frequent infections characterize this ne …
The CMT2B (Charcot-Marie-Tooth type 2B) disease is an autosomal dominant axonal neuropathy. Sensor …
Autosomal dominant inherited neuropathies with prominent sensory loss and mutilations: a review.
Auer-Grumbach M, De Jonghe P, Verhoeven K, Timmerman V, Wagner K, Hartung HP, Nicholson GA. Auer-Grumbach M, et al. Arch Neurol. 2003 Mar;60(3):329-34. doi: 10.1001/archneur.60.3.329. Arch Neurol. 2003. PMID: 12633143 Review.
Molecular genetic studies of autosomal dominant inherited neuropathies with prominent sensory loss and ulceromutilating features have assigned the genetic loci for HMSN type 2B (Charcot-Marie-Tooth syndrome type 2B) and HSN type
Molecular genetic studies of autosomal dominant inherited neuropathies with prominent sensory loss and ulceromutilating features have assign …