STH

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Saitohin
Identifiers
Symbol(s) STH; MGC163191; MGC163193
External IDs OMIM: 607067 HomoloGene: 88448
Orthologs
Human Mouse
Entrez 246744 n/a


Refseq NM_001007532 (mRNA)
NP_001007533 (protein)		 n/a (mRNA)
n/a (protein)
Pubmed search [1] n/a

Saitohin, also known as STH, is a human gene.[1]


[edit] References

  1. ^ Entrez Gene: STH saitohin.

[edit] 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.". Nature 377 (6547 Suppl): 3–174. PMID 7566098. 
  • Conrad C, Vianna C, Freeman M, Davies P (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. PMID 12032355. 
  • 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. 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. PMID 12932819. 
  • Gao L, Tse SW, Conrad C, Andreadis A (2006). "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. 
  • 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. 
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