File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1016/j.neuint.2012.06.014
- Scopus: eid_2-s2.0-84867494020
- PMID: 22749857
- WOS: WOS:000310946100014
- Find via
Supplementary
- Citations:
- Appears in Collections:
Article: Scaffold protein Homer 1: Implications for neurological diseases
Title | Scaffold protein Homer 1: Implications for neurological diseases |
---|---|
Authors | |
Keywords | Addiction Fragile X syndrome Homer protein Metabotropic glutamate receptor Neuropathic pain Postsynaptic density Schizophrenia Transient receptor potential channel Traumatic brain injury X-linked mental retardation |
Issue Date | 2012 |
Citation | Neurochemistry International, 2012, v. 61, n. 5, p. 731-738 How to Cite? |
Abstract | Homer proteins are commonly known as scaffold proteins at postsynaptic density. Homer 1 is a widely studied member of the Homer protein family, comprising both synaptic structure and mediating postsynaptic signaling transduction. Both an immediate-early gene encoding a Homer 1 variant and a constitutively expressed Homer 1 variant regulate receptor clustering and trafficking, intracellular calcium homeostasis, and intracellular molecule complex formation. Substantial preclinical investigations have implicated that each of these Homer 1 variants are associated with the etiology of many neurological diseases, such as pain, mental retardation syndromes, Alzheimer's disease, schizophrenia, drug-induced addiction, and traumatic brain injury. © 2012 Elsevier Ltd. All rights reserved. |
Persistent Identifier | http://hdl.handle.net/10722/325249 |
ISSN | 2023 Impact Factor: 4.4 2023 SCImago Journal Rankings: 1.049 |
ISI Accession Number ID |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Luo, Peng | - |
dc.contributor.author | Li, Xia | - |
dc.contributor.author | Fei, Zhou | - |
dc.contributor.author | Poon, Waisang | - |
dc.date.accessioned | 2023-02-27T07:30:57Z | - |
dc.date.available | 2023-02-27T07:30:57Z | - |
dc.date.issued | 2012 | - |
dc.identifier.citation | Neurochemistry International, 2012, v. 61, n. 5, p. 731-738 | - |
dc.identifier.issn | 0197-0186 | - |
dc.identifier.uri | http://hdl.handle.net/10722/325249 | - |
dc.description.abstract | Homer proteins are commonly known as scaffold proteins at postsynaptic density. Homer 1 is a widely studied member of the Homer protein family, comprising both synaptic structure and mediating postsynaptic signaling transduction. Both an immediate-early gene encoding a Homer 1 variant and a constitutively expressed Homer 1 variant regulate receptor clustering and trafficking, intracellular calcium homeostasis, and intracellular molecule complex formation. Substantial preclinical investigations have implicated that each of these Homer 1 variants are associated with the etiology of many neurological diseases, such as pain, mental retardation syndromes, Alzheimer's disease, schizophrenia, drug-induced addiction, and traumatic brain injury. © 2012 Elsevier Ltd. All rights reserved. | - |
dc.language | eng | - |
dc.relation.ispartof | Neurochemistry International | - |
dc.subject | Addiction | - |
dc.subject | Fragile X syndrome | - |
dc.subject | Homer protein | - |
dc.subject | Metabotropic glutamate receptor | - |
dc.subject | Neuropathic pain | - |
dc.subject | Postsynaptic density | - |
dc.subject | Schizophrenia | - |
dc.subject | Transient receptor potential channel | - |
dc.subject | Traumatic brain injury | - |
dc.subject | X-linked mental retardation | - |
dc.title | Scaffold protein Homer 1: Implications for neurological diseases | - |
dc.type | Article | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1016/j.neuint.2012.06.014 | - |
dc.identifier.pmid | 22749857 | - |
dc.identifier.scopus | eid_2-s2.0-84867494020 | - |
dc.identifier.volume | 61 | - |
dc.identifier.issue | 5 | - |
dc.identifier.spage | 731 | - |
dc.identifier.epage | 738 | - |
dc.identifier.eissn | 1872-9754 | - |
dc.identifier.isi | WOS:000310946100014 | - |