SLC26A8: Difference between revisions

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*{{cite journal | author=Markovich D |title=Physiological roles and regulation of mammalian sulfate transporters. |journal=Physiol. Rev. |volume=81 |issue= 4 |pages= 1499-533 |year= 2001 |pmid= 11581495 |doi= }}
*{{cite journal | author=Markovich D |title=Physiological roles and regulation of mammalian sulfate transporters. |journal=Physiol. Rev. |volume=81 |issue= 4 |pages= 1499–533 |year= 2001 |pmid= 11581495 |doi= }}
*{{cite journal | author=Mäkelä S, Eklund R, Lähdetie J, ''et al.'' |title=Mutational analysis of the human SLC26A8 gene: exclusion as a candidate for male infertility due to primary spermatogenic failure. |journal=Mol. Hum. Reprod. |volume=11 |issue= 2 |pages= 129-32 |year= 2005 |pmid= 15579655 |doi= 10.1093/molehr/gah140 }}
*{{cite journal | author=Mäkelä S, Eklund R, Lähdetie J, ''et al.'' |title=Mutational analysis of the human SLC26A8 gene: exclusion as a candidate for male infertility due to primary spermatogenic failure. |journal=Mol. Hum. Reprod. |volume=11 |issue= 2 |pages= 129–32 |year= 2005 |pmid= 15579655 |doi= 10.1093/molehr/gah140 }}
*{{cite journal | author=Ota T, Suzuki Y, Nishikawa T, ''et al.'' |title=Complete sequencing and characterization of 21,243 full-length human cDNAs. |journal=Nat. Genet. |volume=36 |issue= 1 |pages= 40-5 |year= 2004 |pmid= 14702039 |doi= 10.1038/ng1285 }}
*{{cite journal | author=Ota T, Suzuki Y, Nishikawa T, ''et al.'' |title=Complete sequencing and characterization of 21,243 full-length human cDNAs. |journal=Nat. Genet. |volume=36 |issue= 1 |pages= 40–5 |year= 2004 |pmid= 14702039 |doi= 10.1038/ng1285 }}
*{{cite journal | author=Strausberg RL, Feingold EA, Grouse LH, ''et al.'' |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 }}
*{{cite journal | author=Strausberg RL, Feingold EA, Grouse LH, ''et al.'' |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 }}
*{{cite journal | author=Lohi H, Kujala M, Makela S, ''et al.'' |title=Functional characterization of three novel tissue-specific anion exchangers SLC26A7, -A8, and -A9. |journal=J. Biol. Chem. |volume=277 |issue= 16 |pages= 14246-54 |year= 2002 |pmid= 11834742 |doi= 10.1074/jbc.M111802200 }}
*{{cite journal | author=Lohi H, Kujala M, Makela S, ''et al.'' |title=Functional characterization of three novel tissue-specific anion exchangers SLC26A7, -A8, and -A9. |journal=J. Biol. Chem. |volume=277 |issue= 16 |pages= 14246–54 |year= 2002 |pmid= 11834742 |doi= 10.1074/jbc.M111802200 }}
*{{cite journal | author=Vincourt JB, Jullien D, Kossida S, ''et al.'' |title=Molecular cloning of SLC26A7, a novel member of the SLC26 sulfate/anion transporter family, from high endothelial venules and kidney. |journal=Genomics |volume=79 |issue= 2 |pages= 249-56 |year= 2002 |pmid= 11829495 |doi= 10.1006/geno.2002.6689 }}
*{{cite journal | author=Vincourt JB, Jullien D, Kossida S, ''et al.'' |title=Molecular cloning of SLC26A7, a novel member of the SLC26 sulfate/anion transporter family, from high endothelial venules and kidney. |journal=Genomics |volume=79 |issue= 2 |pages= 249–56 |year= 2002 |pmid= 11829495 |doi= 10.1006/geno.2002.6689 }}
*{{cite journal | author=Toure A, Morin L, Pineau C, ''et al.'' |title=Tat1, a novel sulfate transporter specifically expressed in human male germ cells and potentially linked to rhogtpase signaling. |journal=J. Biol. Chem. |volume=276 |issue= 23 |pages= 20309-15 |year= 2001 |pmid= 11278976 |doi= 10.1074/jbc.M011740200 }}
*{{cite journal | author=Toure A, Morin L, Pineau C, ''et al.'' |title=Tat1, a novel sulfate transporter specifically expressed in human male germ cells and potentially linked to rhogtpase signaling. |journal=J. Biol. Chem. |volume=276 |issue= 23 |pages= 20309–15 |year= 2001 |pmid= 11278976 |doi= 10.1074/jbc.M011740200 }}
*{{cite journal | author=Mocellin R, Bühlmeyer K |title=Late banding operation in children with ventricular septal defect and pulmonary arterial hypertension. |journal=European journal of cardiology |volume=3 |issue= 3 |pages= 205-11 |year= 1976 |pmid= 1183472 |doi= }}
*{{cite journal | author=Mocellin R, Bühlmeyer K |title=Late banding operation in children with ventricular septal defect and pulmonary arterial hypertension. |journal=European journal of cardiology |volume=3 |issue= 3 |pages= 205–11 |year= 1976 |pmid= 1183472 |doi= }}
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Revision as of 15:37, 15 May 2009

Template:PBB Solute carrier family 26, member 8, also known as SLC26A8, is a human gene.[1]

Template:PBB Summary

References

  1. ^ "Entrez Gene: SLC26A8 solute carrier family 26, member 8".

Further reading

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