Alpha-tocopherol transfer protein: Difference between revisions

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{{Infobox_gene}}
'''Alpha-tocopherol transfer protein''' is a [[protein]] that in humans is encoded by the ''TTPA'' [[gene]].<ref name="pmid7719340">{{cite journal | vauthors = Ouahchi K, Arita M, Kayden H, Hentati F, Ben Hamida M, Sokol R, Arai H, Inoue K, Mandel JL, Koenig M | title = Ataxia with isolated vitamin E deficiency is caused by mutations in the alpha-tocopherol transfer protein | journal = Nat Genet | volume = 9 | issue = 2 | pages = 141–5 |date=May 1995 | pmid = 7719340 | pmc =  | doi = 10.1038/ng0295-141 }}</ref><ref name="pmid7887897">{{cite journal | vauthors = Arita M, Sato Y, Miyata A, Tanabe T, Takahashi E, Kayden HJ, Arai H, Inoue K | title = Human alpha-tocopherol transfer protein: cDNA cloning, expression and chromosomal localization | journal = Biochem J | volume = 306 | issue =  2| pages = 437–43 |date=Apr 1995 | pmid = 7887897 | pmc = 1136538 | doi = }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: TTPA tocopherol (alpha) transfer protein (ataxia (Friedreich-like) with vitamin E deficiency)| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=7274| accessdate = }}</ref>
'''Alpha-tocopherol transfer protein''' is a [[protein]] that in humans is encoded by the ''TTPA'' [[gene]].<ref name=Ouahchi1995>{{cite journal | vauthors = Ouahchi K, Arita M, Kayden H, Hentati F, Ben Hamida M, Sokol R, Arai H, Inoue K, Mandel JL, Koenig M | title = Ataxia with isolated vitamin E deficiency is caused by mutations in the alpha-tocopherol transfer protein | journal = Nat Genet | volume = 9 | issue = 2 | pages = 141–145 |date=1995 | pmid = 7719340 | pmc =  | doi = 10.1038/ng0295-141}}</ref><ref name=Arita1995>{{cite journal | vauthors = Arita M, Sato Y, Miyata A, Tanabe T, Takahashi E, Kayden HJ, Arai H, Inoue K | title = Human alpha-tocopherol transfer protein: cDNA cloning, expression and chromosomal localization | journal = Biochem J | volume = 306 | issue =  2| pages = 437–443 |date=1995 | pmid = 7887897 | pmc = 1136538 | doi =}}</ref><ref name=EntrezGene>{{cite web | title = Entrez Gene: TTPA tocopherol (alpha) transfer protein (ataxia (Friedreich-like) with vitamin E deficiency)| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=7274| accessdate =}}</ref>


==See also==
==See also==

Revision as of 16:24, 30 August 2018

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

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RefSeq (protein)

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

Alpha-tocopherol transfer protein is a protein that in humans is encoded by the TTPA gene.[1][2][3]

See also

References

  1. Ouahchi K, Arita M, Kayden H, Hentati F, Ben Hamida M, Sokol R, Arai H, Inoue K, Mandel JL, Koenig M (1995). "Ataxia with isolated vitamin E deficiency is caused by mutations in the alpha-tocopherol transfer protein". Nat Genet. 9 (2): 141–145. doi:10.1038/ng0295-141. PMID 7719340.
  2. Arita M, Sato Y, Miyata A, Tanabe T, Takahashi E, Kayden HJ, Arai H, Inoue K (1995). "Human alpha-tocopherol transfer protein: cDNA cloning, expression and chromosomal localization". Biochem J. 306 (2): 437–443. PMC 1136538. PMID 7887897.
  3. "Entrez Gene: TTPA tocopherol (alpha) transfer protein (ataxia (Friedreich-like) with vitamin E deficiency)".

Further reading

External links