(Q46633766)

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Prenylation-defective human connexin32 mutants are normally localized and function equivalently to wild-type connexin32 in myelinating Schwann cells.

scientific article published in August 2005

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16079393%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

Prenylation-defective human connexin32 mutants are normally localized and function equivalently to wild-type connexin32 in myelinating Schwann cells (English)

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16079393%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

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Steven S. Scherer

4

object named as

Steven S Scherer

1 reference

Europe PubMed Central

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5 January 2020

author name string

Yan Huang

1

1 reference

Europe PubMed Central

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5 January 2020

Erich E Sirkowski

2

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16079393%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

John T Stickney

3

1 reference

Europe PubMed Central

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5 January 2020

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publication date

1 August 2005

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5 January 2020

Journal of Neuroscience

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16079393%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

25

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Europe PubMed Central

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5 January 2020

31

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16079393%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

7111-7120

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16079393%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

Altered formation of hemichannels and gap junction channels caused by C-terminal connexin-32 mutations.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Studies in transgenic mice indicate a loss of connexin32 function in X-linked Charcot-Marie-Tooth disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The prostacyclin receptor is isoprenylated. Isoprenylation is required for efficient receptor-effector coupling.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A unique mutation in connexin32 associated with severe, early onset CMTX in a heterozygous female

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Myelinating Schwann cells determine the internodal localization of Kv1.1, Kv1.2, Kvbeta2, and Caspr.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in connexin 32: the molecular and biophysical bases for the X-linked form of Charcot-Marie-Tooth disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-Linked Charcot-Marie-Tooth disease with a new mutation (Thr191Ala) in the connexin32

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Functional alterations in gap junction channels formed by mutant forms of connexin 32: evidence for loss of function as a pathogenic mechanism in the X-linked form of Charcot-Marie-Tooth disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structural and functional diversity of connexin genes in the mouse and human genome

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Connexin29 is uniquely distributed within myelinating glial cells of the central and peripheral nervous systems.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Connexin29 expression, immunocytochemistry and freeze-fracture replica immunogold labelling (FRIL) in sciatic nerve

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nogo-A expressed in Schwann cells impairs axonal regeneration after peripheral nerve injury

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diverse trafficking abnormalities of connexin32 mutants causing CMTX

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tamoxifen-inducible glia-specific Cre mice for somatic mutagenesis in oligodendrocytes and Schwann cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

G protein beta gamma subunits synthesized in Sf9 cells. Functional characterization and the significance of prenylation of gamma

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Specific localization and timing in neuronal signal transduction mediated by protein-lipid interactions.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pathogenesis of X-linked Charcot-Marie-Tooth disease: differential effects of two mutations in connexin 32

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Testing antivirals against hepatitis delta virus: farnesyl transferase inhibitors

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Connexin32-containing gap junctions in Schwann cells at the internodal zone of partial myelin compaction and in Schmidt-Lanterman incisures

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutational analysis of PMP22, MPZ, GJB1, EGR2 and NEFL in Korean Charcot-Marie-Tooth neuropathy patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transgenic expression of human connexin32 in myelinating Schwann cells prevents demyelination in connexin32-null mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Severe neuropathy with leaky connexin32 hemichannels.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tight junctions in Schwann cells of peripheral myelinated axons: a lesson from claudin-19-deficient mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of a prenylation site in delta virus large antigen

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isoprenoid addition to Ras protein is the critical modification for its membrane association and transforming activity

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The myelin-associated glycoproteins: membrane disposition, evidence of a novel disulfide linkage between immunoglobulin-like domains, and posttranslational palmitylation.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Farnesol modification of Kirsten-ras exon 4B protein is essential for transformation

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked dominant hereditary motor and sensory neuropathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Co-localization of the myelin-associated glycoprotein and the microfilament components, F-actin and spectrin, in Schwann cells of myelinated nerve fibres

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

All ras proteins are polyisoprenylated but only some are palmitoylated

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Motoneurons of the rat sciatic nerve

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Factors affecting the efficiency of introducing foreign DNA into mice by microinjecting eggs

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A rhodopsin gene mutation responsible for autosomal dominant retinitis pigmentosa results in a protein that is defective in localization to the photoreceptor outer segment

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deficient geranylgeranylation of Ram/Rab27 in choroideremia.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Efficient Interaction with a Receptor Requires a Specific Type of Prenyl Group on the G Protein γ Subunit

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Use of alternate promoters for tissue-specific expression of the gene coding for connexin32

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multisubunit assembly of an integral plasma membrane channel protein, gap junction connexin43, occurs after exit from the ER.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel E-cadherin-mediated adhesion in peripheral nerve: Schwann cell architecture is stabilized by autotypic adherens junctions

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lipid modifications of G proteins

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isoprenylated proteins in myelin.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Connexin mutations in X-linked Charcot-Marie-Tooth disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Benzodiazepine peptidomimetics: potent inhibitors of Ras farnesylation in animal cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The effect of posttranslational modifications on the interaction of Ras2 with adenylyl cyclase

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Connexin32 is a myelin-related protein in the PNS and CNS

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Connections with connexins: the molecular basis of direct intercellular signaling

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Synthesis and assembly of human beta 1 gap junctions in BHK cells by DNA transfection with the human beta 1 cDNA.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Correlation between connexin 32 gene mutations and clinical phenotype in X-linked dominant Charcot-Marie-Tooth neuropathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Defective propagation of signals generated by sympathetic nerve stimulation in the liver of connexin32-deficient mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Protein prenylation: molecular mechanisms and functional consequences

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The human connexin32 gene is transcribed from two tissue-specific promoters

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Altered connexin expression after peripheral nerve injury

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A second alternative transcript of the gap junction gene connexin32 is expressed in murine Schwann cells and modulated in injured sciatic nerve

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Connexin32 in oligodendrocytes and association with myelinated fibers in mouse and rat brain.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structural abnormalities and deficient maintenance of peripheral nerve myelin in mice lacking the gap junction protein connexin 32

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Charcot-Marie-Tooth disease type 1A with 17p11.2 duplication. Clinical and electrophysiological phenotype study and factors influencing disease severity in 119 cases.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Changes in permeability caused by connexin 32 mutations underlie X-linked Charcot-Marie-Tooth disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel mutation (C201R) in the transmembrane domain of connexin 32 in severe X-linked Charcot-Marie-Tooth disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The first de novo mutation of the connexin 32 gene associated with X linked Charcot-Marie-Tooth disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spectrum of mutations in Finnish patients with Charcot-Marie-Tooth disease and related neuropathies

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Connexin32-null mice develop demyelinating peripheral neuropathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Functional gap junctions in the schwann cell myelin sheath

1 reference

https://pubmed.ncbi.nlm.nih.gov/16079393

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1523/JNEUROSCI.1319-05.2005

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16079393%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16079393%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16079393%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

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