(Q24317547)

Lipopolysaccharide induced TNF factor

GOA release 2020-03-11

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GOA release 2020-03-11

author name string

Andrew J Shirk

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Susan K Anderson

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Sayed H Hashemi

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Phillip F Chance

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Craig L Bennett

Journal of Neuroscience Research

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language of work or name

English

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publication date

1 October 2005

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published in

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volume

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issue

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page(s)

43-50

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cites work

SIMPLE mutation in demyelinating neuropathy and distribution in sciatic nerve

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Identification of protein-protein interactions using in vivo cross-linking and mass spectrometry

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PMP22 accumulation in aggresomes: implications for CMT1A pathology

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Aggresome formation in neuropathy models based on peripheral myelin protein 22 mutations

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Recessive, but not dominant, mutations in peripheral myelin protein 22 gene show unique patterns of aggregation and intracellular trafficking.

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WWOX binds the specific proline-rich ligand PPXY: identification of candidate interacting proteins

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Identification of multiple proteins expressed in murine embryos as binding partners for the WW domains of the ubiquitin-protein ligase Nedd4

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TSG101 interaction with HRS mediates endosomal trafficking and receptor down-regulation

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Cell cycle-dependent subcellular localization of the TSG101 protein and mitotic and nuclear abnormalities associated with TSG101 deficiency

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The C2 domain of the ubiquitin protein ligase Nedd4 mediates Ca2+-dependent plasma membrane localization

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Mycobacterium bovis Bacillus Calmette-Guerin and its cell wall complex induce a novel lysosomal membrane protein, SIMPLE, that bridges the missing link between lipopolysaccharide and p53-inducible gene, LITAF(PIG7), and estrogen-inducible gene, EET-1

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Vps27 recruits ESCRT machinery to endosomes during MVB sorting

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Mapping of Charcot-Marie-Tooth disease type 1C to chromosome 16p identifies a novel locus for demyelinating neuropathies

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Localization of the Rsp5p ubiquitin-protein ligase at multiple sites within the endocytic pathway

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Signals for sorting of transmembrane proteins to endosomes and lysosomes

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Analysis of the DNA duplication 17p11.2 in Charcot-Marie-Tooth neuropathy type 1 pedigrees: additional evidence for a third autosomal CMT1 locus

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Mutation of a putative protein degradation gene LITAF/SIMPLE in Charcot-Marie-Tooth disease 1C.

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Upregulation of the endosomal-lysosomal pathway in the trembler-J neuropathy.

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Neurons promote the translocation of peripheral myelin protein 22 into myelin

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New chemical crosslinking methods for the identification of transient protein-protein interactions with multiprotein complexes.

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Identifiers

DOI

10.1002/JNR.20628

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Consolidated OpenCitations Corpus – April 2017

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Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

16118794

1 reference

Consolidated OpenCitations Corpus – April 2017