SERPINI1: Difference between revisions

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*{{cite journal  |author1=Barker-Carlson K |author2=Lawrence DA |author3=Schwartz BS |title=Acyl-enzyme complexes between tissue-type plasminogen activator and neuroserpin are short-lived in vitro. |journal=J. Biol. Chem. |volume=277 |issue= 49 |pages= 46852–7 |year= 2003 |pmid= 12228252 |doi= 10.1074/jbc.M207740200 }}
*{{cite journal  |author1=Barker-Carlson K |author2=Lawrence DA |author3=Schwartz BS |title=Acyl-enzyme complexes between tissue-type plasminogen activator and neuroserpin are short-lived in vitro. |journal=J. Biol. Chem. |volume=277 |issue= 49 |pages= 46852–7 |year= 2003 |pmid= 12228252 |doi= 10.1074/jbc.M207740200 }}
*{{cite journal  |vauthors=Parmar PK, Coates LC, Pearson JF, etal |title=Neuroserpin regulates neurite outgrowth in nerve growth factor-treated PC12 cells. |journal=J. Neurochem. |volume=82 |issue= 6 |pages= 1406–15 |year= 2002 |pmid= 12354288 |doi=10.1046/j.1471-4159.2002.01100.x  }}
*{{cite journal  |vauthors=Parmar PK, Coates LC, Pearson JF, etal |title=Neuroserpin regulates neurite outgrowth in nerve growth factor-treated PC12 cells. |journal=J. Neurochem. |volume=82 |issue= 6 |pages= 1406–15 |year= 2002 |pmid= 12354288 |doi=10.1046/j.1471-4159.2002.01100.x  }}
*{{cite journal  |vauthors=Strausberg RL, Feingold EA, Grouse LH, etal |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899  | pmc=139241 }}
*{{cite journal  |vauthors=Strausberg RL, Feingold EA, Grouse LH, etal |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899  | pmc=139241 |bibcode=2002PNAS...9916899M }}
*{{cite journal  |author1=Miranda E |author2=Römisch K |author3=Lomas DA |title=Mutants of neuroserpin that cause dementia accumulate as polymers within the endoplasmic reticulum. |journal=J. Biol. Chem. |volume=279 |issue= 27 |pages= 28283–91 |year= 2004 |pmid= 15090543 |doi= 10.1074/jbc.M313166200 }}
*{{cite journal  |author1=Miranda E |author2=Römisch K |author3=Lomas DA |title=Mutants of neuroserpin that cause dementia accumulate as polymers within the endoplasmic reticulum. |journal=J. Biol. Chem. |volume=279 |issue= 27 |pages= 28283–91 |year= 2004 |pmid= 15090543 |doi= 10.1074/jbc.M313166200 }}
*{{cite journal  |vauthors=Teesalu T, Kulla A, Simisker A, etal |title=Tissue plasminogen activator and neuroserpin are widely expressed in the human central nervous system. |journal=Thromb. Haemost. |volume=92 |issue= 2 |pages= 358–68 |year= 2005 |pmid= 15269833 |doi= 10.1267/THRO04080358 }}
*{{cite journal  |vauthors=Teesalu T, Kulla A, Simisker A, etal |title=Tissue plasminogen activator and neuroserpin are widely expressed in the human central nervous system. |journal=Thromb. Haemost. |volume=92 |issue= 2 |pages= 358–68 |year= 2005 |pmid= 15269833 |doi= 10.1267/THRO04080358 }}
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*{{cite journal  |vauthors=Gerhard DS, Wagner L, Feingold EA, etal |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121–7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504  | pmc=528928 }}
*{{cite journal  |vauthors=Gerhard DS, Wagner L, Feingold EA, etal |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121–7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504  | pmc=528928 }}
*{{cite journal  |author1=Onda M |author2=Belorgey D |author3=Sharp LK |author4=Lomas DA |title=Latent S49P neuroserpin forms polymers in the dementia familial encephalopathy with neuroserpin inclusion bodies. |journal=J. Biol. Chem. |volume=280 |issue= 14 |pages= 13735–41 |year= 2005 |pmid= 15664988 |doi= 10.1074/jbc.M413282200 }}
*{{cite journal  |author1=Onda M |author2=Belorgey D |author3=Sharp LK |author4=Lomas DA |title=Latent S49P neuroserpin forms polymers in the dementia familial encephalopathy with neuroserpin inclusion bodies. |journal=J. Biol. Chem. |volume=280 |issue= 14 |pages= 13735–41 |year= 2005 |pmid= 15664988 |doi= 10.1074/jbc.M413282200 }}
*{{cite journal  |vauthors=Rual JF, Venkatesan K, Hao T, etal |title=Towards a proteome-scale map of the human protein-protein interaction network. |journal=Nature |volume=437 |issue= 7062 |pages= 1173–8 |year= 2005 |pmid= 16189514 |doi= 10.1038/nature04209 }}
*{{cite journal  |vauthors=Rual JF, Venkatesan K, Hao T, etal |title=Towards a proteome-scale map of the human protein-protein interaction network. |journal=Nature |volume=437 |issue= 7062 |pages= 1173–8 |year= 2005 |pmid= 16189514 |doi= 10.1038/nature04209 |bibcode=2005Natur.437.1173R }}
*{{cite journal  |vauthors=Kinghorn KJ, Crowther DC, Sharp LK, etal |title=Neuroserpin binds Abeta and is a neuroprotective component of amyloid plaques in Alzheimer disease. |journal=J. Biol. Chem. |volume=281 |issue= 39 |pages= 29268–77 |year= 2006 |pmid= 16849336 |doi= 10.1074/jbc.M600690200 }}
*{{cite journal  |vauthors=Kinghorn KJ, Crowther DC, Sharp LK, etal |title=Neuroserpin binds Abeta and is a neuroprotective component of amyloid plaques in Alzheimer disease. |journal=J. Biol. Chem. |volume=281 |issue= 39 |pages= 29268–77 |year= 2006 |pmid= 16849336 |doi= 10.1074/jbc.M600690200 }}
*{{cite journal  |vauthors=Chen PY, Chang WS, Chou RH, etal |title=Two non-homologous brain diseases-related genes, SERPINI1 and PDCD10, are tightly linked by an asymmetric bidirectional promoter in an evolutionarily conserved manner. |journal=BMC Mol. Biol. |volume=8 |issue=  |pages= 2 |year= 2007 |pmid= 17212813 |doi= 10.1186/1471-2199-8-2  | pmc=1796892 }}
*{{cite journal  |vauthors=Chen PY, Chang WS, Chou RH, etal |title=Two non-homologous brain diseases-related genes, SERPINI1 and PDCD10, are tightly linked by an asymmetric bidirectional promoter in an evolutionarily conserved manner. |journal=BMC Mol. Biol. |volume=8 |issue=  |pages= 2 |year= 2007 |pmid= 17212813 |doi= 10.1186/1471-2199-8-2  | pmc=1796892 }}

Latest revision as of 04:32, 26 June 2018

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Identifiers
Aliases
External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

n/a

n/a

RefSeq (protein)

n/a

n/a

Location (UCSC)n/an/a
PubMed searchn/an/a
Wikidata
View/Edit Human

Neuroserpin is a protein that in humans is encoded by the SERPINI1 gene.[1]

It is associated with Familial encephalopathy with neuroserpin inclusion bodies.

Serine protease inhibitors of the serpin superfamily are involved in many cellular processes. Neuroserpin was first identified as a protein secreted from the axons of dorsal root ganglion neurons (Stoeckli et al., 1989). It is expressed in the late stages of neurogenesis during the process of synapse formation.[supplied by OMIM][1]

Interactions

SERPINI1 has been shown to interact with Tissue plasminogen activator.[2]

References

  1. 1.0 1.1 "Entrez Gene: SERPINI1 serpin peptidase inhibitor, clade I (neuroserpin), member 1".
  2. Parmar, Parmjeet K; Coates Leigh C; Pearson John F; Hill Rena M; Birch Nigel P (September 2002). "Neuroserpin regulates neurite outgrowth in nerve growth factor-treated PC12 cells". J. Neurochem. England. 82 (6): 1406–15. doi:10.1046/j.1471-4159.2002.01100.x. ISSN 0022-3042. PMID 12354288.

Further reading

External links

  • The MEROPS online database for peptidases and their inhibitors: I04.025