STH (gene): Difference between revisions
Jump to navigation
Jump to search
m Bot: HTTP→HTTPS |
imported>JCW-CleanerBot m →Further reading: task, replaced: Neuro-degenerative diseases → Neuro-Degenerative Diseases using AWB |
||
Line 1: | Line 1: | ||
{{Underlinked|date= | {{Underlinked|date=March 2018}} | ||
{{Infobox_gene}} | {{Infobox_gene}} | ||
'''Saitohin''' is a [[protein]] that in humans is encoded by the ''STH'' [[gene]].<ref name="pmid12032355">{{cite journal | vauthors = Conrad C, Vianna C, Freeman M, Davies P | title = A polymorphic gene nested within an intron of the tau gene: implications for Alzheimer's disease | journal = Proc Natl Acad Sci U S A | volume = 99 | issue = 11 | pages = 7751–6 |date=May 2002 | pmid = 12032355 | pmc = 124341 | doi = 10.1073/pnas.112194599 }}</ref><ref name="pmid16186110">{{cite journal | vauthors = Gao L, Tse SW, Conrad C, Andreadis A | title = Saitohin, which is nested in the tau locus and confers allele-specific susceptibility to several neurodegenerative diseases, interacts with peroxiredoxin 6 | journal = J Biol Chem | volume = 280 | issue = 47 | pages = 39268–72 |date=Nov 2005 | pmid = 16186110 | pmc = | doi = 10.1074/jbc.M506116200 }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: STH saitohin| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=246744| accessdate = }}</ref> | '''Saitohin''' is a [[protein]] that in humans is encoded by the ''STH'' [[gene]].<ref name="pmid12032355">{{cite journal | vauthors = Conrad C, Vianna C, Freeman M, Davies P | title = A polymorphic gene nested within an intron of the tau gene: implications for Alzheimer's disease | journal = Proc Natl Acad Sci U S A | volume = 99 | issue = 11 | pages = 7751–6 |date=May 2002 | pmid = 12032355 | pmc = 124341 | doi = 10.1073/pnas.112194599 }}</ref><ref name="pmid16186110">{{cite journal | vauthors = Gao L, Tse SW, Conrad C, Andreadis A | title = Saitohin, which is nested in the tau locus and confers allele-specific susceptibility to several neurodegenerative diseases, interacts with peroxiredoxin 6 | journal = J Biol Chem | volume = 280 | issue = 47 | pages = 39268–72 |date=Nov 2005 | pmid = 16186110 | pmc = | doi = 10.1074/jbc.M506116200 }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: STH saitohin| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=246744| accessdate = }}</ref> | ||
Line 19: | Line 19: | ||
*{{cite journal |vauthors=Cook L, Brayne CE, Easton D, etal |title=No evidence for an association between Saitohin Q7R polymorphism and Alzheimer's disease. |journal=Ann. Neurol. |volume=52 |issue= 5 |pages= 690–1 |year= 2002 |pmid= 12402275 |doi= 10.1002/ana.10362 }} | *{{cite journal |vauthors=Cook L, Brayne CE, Easton D, etal |title=No evidence for an association between Saitohin Q7R polymorphism and Alzheimer's disease. |journal=Ann. Neurol. |volume=52 |issue= 5 |pages= 690–1 |year= 2002 |pmid= 12402275 |doi= 10.1002/ana.10362 }} | ||
*{{cite journal |vauthors=Verpillat P, Ricard S, Hannequin D, etal |title=Is the saitohin gene involved in neurodegenerative diseases? |journal=Ann. Neurol. |volume=52 |issue= 6 |pages= 829–32 |year= 2002 |pmid= 12447938 |doi= 10.1002/ana.10384 }} | *{{cite journal |vauthors=Verpillat P, Ricard S, Hannequin D, etal |title=Is the saitohin gene involved in neurodegenerative diseases? |journal=Ann. Neurol. |volume=52 |issue= 6 |pages= 829–32 |year= 2002 |pmid= 12447938 |doi= 10.1002/ana.10384 }} | ||
*{{cite journal |vauthors=Zekanowski C, Pepłońska B, Styczyńska M, etal |title=Mutation screening of the MAPT and STH genes in Polish patients with clinically diagnosed frontotemporal dementia. |journal=Dementia and | *{{cite journal |vauthors=Zekanowski C, Pepłońska B, Styczyńska M, etal |title=Mutation screening of the MAPT and STH genes in Polish patients with clinically diagnosed frontotemporal dementia. |journal=Dementia and Geriatric Cognitive Disorders |volume=16 |issue= 3 |pages= 126–31 |year= 2003 |pmid= 12826737 |doi= 10.1159/000070999 }} | ||
*{{cite journal |vauthors=Combarros O, Rodero L, Infante J, etal |title=Age-dependent association between the Q7R polymorphism in the Saitohin gene and sporadic Alzheimer's disease. |journal=Dementia and | *{{cite journal |vauthors=Combarros O, Rodero L, Infante J, etal |title=Age-dependent association between the Q7R polymorphism in the Saitohin gene and sporadic Alzheimer's disease. |journal=Dementia and Geriatric Cognitive Disorders |volume=16 |issue= 3 |pages= 132–5 |year= 2003 |pmid= 12826738 |doi= 10.1159/000071000 }} | ||
*{{cite journal |vauthors=de Silva R, Hope A, Pittman A, etal |title=Strong association of the Saitohin gene Q7 variant with progressive supranuclear palsy. |journal=Neurology |volume=61 |issue= 3 |pages= 407–9 |year= 2004 |pmid= 12913211 |doi= 10.1212/01.wnl.0000073140.25533.90}} | *{{cite journal |vauthors=de Silva R, Hope A, Pittman A, etal |title=Strong association of the Saitohin gene Q7 variant with progressive supranuclear palsy. |journal=Neurology |volume=61 |issue= 3 |pages= 407–9 |year= 2004 |pmid= 12913211 |doi= 10.1212/01.wnl.0000073140.25533.90}} | ||
*{{cite journal |vauthors=Pepłońska B, Zekanowski C, Religa D, etal |title=Strong association between Saitohin gene polymorphism and tau haplotype in the Polish population. |journal=Neurosci. Lett. |volume=348 |issue= 3 |pages= 163–6 |year= 2003 |pmid= 12932819 |doi=10.1016/S0304-3940(03)00788-2 }} | *{{cite journal |vauthors=Pepłońska B, Zekanowski C, Religa D, etal |title=Strong association between Saitohin gene polymorphism and tau haplotype in the Polish population. |journal=Neurosci. Lett. |volume=348 |issue= 3 |pages= 163–6 |year= 2003 |pmid= 12932819 |doi=10.1016/S0304-3940(03)00788-2 }} | ||
*{{cite journal |vauthors=Johansson A, Zetterberg H, Håkansson A, etal |title=TAU haplotype and the Saitohin Q7R gene polymorphism do not influence CSF Tau in Alzheimer's disease and are not associated with frontotemporal dementia or Parkinson's disease. |journal=Neuro- | *{{cite journal |vauthors=Johansson A, Zetterberg H, Håkansson A, etal |title=TAU haplotype and the Saitohin Q7R gene polymorphism do not influence CSF Tau in Alzheimer's disease and are not associated with frontotemporal dementia or Parkinson's disease. |journal=Neuro-Degenerative Diseases |volume=2 |issue= 1 |pages= 28–35 |year= 2006 |pmid= 16909000 |doi= 10.1159/000086428 }} | ||
}} | }} | ||
{{refend}} | {{refend}} |
Latest revision as of 03:53, 3 April 2018
This article needs more links to other articles to help integrate it into the encyclopedia. (March 2018) (Learn how and when to remove this template message) |
VALUE_ERROR (nil) | |||||||
---|---|---|---|---|---|---|---|
Identifiers | |||||||
Aliases | |||||||
External IDs | GeneCards: [1] | ||||||
Orthologs | |||||||
Species | Human | Mouse | |||||
Entrez |
|
| |||||
Ensembl |
|
| |||||
UniProt |
|
| |||||
RefSeq (mRNA) |
|
| |||||
RefSeq (protein) |
|
| |||||
Location (UCSC) | n/a | n/a | |||||
PubMed search | n/a | n/a | |||||
Wikidata | |||||||
|
Saitohin is a protein that in humans is encoded by the STH gene.[1][2][3]
References
- ↑ Conrad C, Vianna C, Freeman M, Davies P (May 2002). "A polymorphic gene nested within an intron of the tau gene: implications for Alzheimer's disease". Proc Natl Acad Sci U S A. 99 (11): 7751–6. doi:10.1073/pnas.112194599. PMC 124341. PMID 12032355.
- ↑ Gao L, Tse SW, Conrad C, Andreadis A (Nov 2005). "Saitohin, which is nested in the tau locus and confers allele-specific susceptibility to several neurodegenerative diseases, interacts with peroxiredoxin 6". J Biol Chem. 280 (47): 39268–72. doi:10.1074/jbc.M506116200. PMID 16186110.
- ↑ "Entrez Gene: STH saitohin".
Further reading
- Adams MD, Kerlavage AR, Fleischmann RD, et al. (1995). "Initial assessment of human gene diversity and expression patterns based upon 83 million nucleotides of cDNA sequence" (PDF). Nature. 377 (6547 Suppl): 3–174. PMID 7566098.
- Cook L, Brayne CE, Easton D, et al. (2002). "No evidence for an association between Saitohin Q7R polymorphism and Alzheimer's disease". Ann. Neurol. 52 (5): 690–1. doi:10.1002/ana.10362. PMID 12402275.
- Verpillat P, Ricard S, Hannequin D, et al. (2002). "Is the saitohin gene involved in neurodegenerative diseases?". Ann. Neurol. 52 (6): 829–32. doi:10.1002/ana.10384. PMID 12447938.
- Zekanowski C, Pepłońska B, Styczyńska M, et al. (2003). "Mutation screening of the MAPT and STH genes in Polish patients with clinically diagnosed frontotemporal dementia". Dementia and Geriatric Cognitive Disorders. 16 (3): 126–31. doi:10.1159/000070999. PMID 12826737.
- Combarros O, Rodero L, Infante J, et al. (2003). "Age-dependent association between the Q7R polymorphism in the Saitohin gene and sporadic Alzheimer's disease". Dementia and Geriatric Cognitive Disorders. 16 (3): 132–5. doi:10.1159/000071000. PMID 12826738.
- de Silva R, Hope A, Pittman A, et al. (2004). "Strong association of the Saitohin gene Q7 variant with progressive supranuclear palsy". Neurology. 61 (3): 407–9. doi:10.1212/01.wnl.0000073140.25533.90. PMID 12913211.
- Pepłońska B, Zekanowski C, Religa D, et al. (2003). "Strong association between Saitohin gene polymorphism and tau haplotype in the Polish population". Neurosci. Lett. 348 (3): 163–6. doi:10.1016/S0304-3940(03)00788-2. PMID 12932819.
- Johansson A, Zetterberg H, Håkansson A, et al. (2006). "TAU haplotype and the Saitohin Q7R gene polymorphism do not influence CSF Tau in Alzheimer's disease and are not associated with frontotemporal dementia or Parkinson's disease". Neuro-Degenerative Diseases. 2 (1): 28–35. doi:10.1159/000086428. PMID 16909000.
This protein-related article is a stub. You can help Wikipedia by expanding it. |
Categories:
- Pages with broken file links
- Articles with too few wikilinks from March 2018
- Articles with invalid date parameter in template
- All articles with too few wikilinks
- Articles covered by WikiProject Wikify from March 2018
- All articles covered by WikiProject Wikify
- Genes on human chromosome
- All stub articles
- Protein stubs