SLC22A18: Difference between revisions

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m [Pu372]Add: author2, author3, display-authors, last4, first4, last5, first5, last6, first6, last7, first7, last8, first8, last9, first9. Tweak: author, title. Combined duplicate references.
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{{PBB_Summary
{{PBB_Summary
| section_title =
| section_title =
| summary_text = This gene is one of several tumor-suppressing subtransferable fragments located in the imprinted gene domain of 11p15.5, an important tumor-suppressor gene region. Alterations in this region have been associated with the Beckwith-Wiedemann syndrome, Wilms tumor, rhabdomyosarcoma, adrenocortical carcinoma, and lung, ovarian, and breast cancer. This gene may play a role in malignancies and disease that involve this region as well as the transport of chloroquine- and quinidine-related compounds in the kidney. Two alternative transcripts encoding the same isoform have been described.<ref name="entrez">{{cite web | title = Entrez Gene: SLC22A18 solute carrier family 22 (organic cation transporter), member 18| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=5002| accessdate = }}</ref>
| summary_text = This gene is one of several tumor-suppressing subtransferable fragments located in the imprinted gene domain of 11p15.5, an important tumor-suppressor gene region. Alterations in this region have been associated with the Beckwith-Wiedemann syndrome, Wilms tumor, rhabdomyosarcoma, adrenocortical carcinoma, and lung, ovarian, and breast cancer. This gene may play a role in malignancies and disease that involve this region as well as the transport of chloroquine- and quinidine-related compounds in the kidney. Two alternative transcripts encoding the same isoform have been described.<ref name="entrez" />
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| citations =
| citations =
*{{cite journal | author=Akiyama S |title=[Mechanisms of drug resistance and reversal of the resistance] |journal=Hum. Cell |volume=14 |issue= 4 |pages= 257–60 |year= 2002 |pmid= 11925925 |doi= }}
*{{cite journal | author=Akiyama S |title=[Mechanisms of drug resistance and reversal of the resistance] |journal=Hum. Cell |volume=14 |issue= 4 |pages= 257–60 |year= 2002 |pmid= 11925925 |doi= }}
*{{cite journal | author=Cooper PR, Smilinich NJ, Day CD, ''et al.'' |title=Divergently transcribed overlapping genes expressed in liver and kidney and located in the 11p15.5 imprinted domain. |journal=Genomics |volume=49 |issue= 1 |pages= 38–51 |year= 1998 |pmid= 9570947 |doi= 10.1006/geno.1998.5221 }}
*{{cite journal | author=Cooper PR |title=Divergently transcribed overlapping genes expressed in liver and kidney and located in the 11p15.5 imprinted domain |journal=Genomics |volume=49 |issue= 1 |pages= 38–51 |year= 1998 |pmid= 9570947 |doi= 10.1006/geno.1998.5221 | author2=Smilinich NJ | author3=Day CD | display-authors=3 | last4=Nowak | first4=NJ | last5=Reid | first5=LH | last6=Pearsall | first6=RS | last7=Reece | first7=M | last8=Prawitt | first8=D | last9=Landers | first9=J }}
*{{cite journal | author=Reece M, Prawitt D, Landers J, ''et al.'' |title=Functional characterization of ORCTL2--an organic cation transporter expressed in the renal proximal tubules. |journal=FEBS Lett. |volume=433 |issue= 3 |pages= 245–50 |year= 1998 |pmid= 9744804 |doi=10.1016/S0014-5793(98)00907-7 }}
*{{cite journal | author=Reece M |title=Functional characterization of ORCTL2--an organic cation transporter expressed in the renal proximal tubules |journal=FEBS Lett. |volume=433 |issue= 3 |pages= 245–50 |year= 1998 |pmid= 9744804 |doi=10.1016/S0014-5793(98)00907-7 | author2=Prawitt D | author3=Landers J | display-authors=3 | last4=Kast | first4=C | last5=Gros | first5=P | last6=Housman | first6=D | last7=Zabel | first7=BU | last8=Pelletier | first8=J }}
*{{cite journal | author=Lee MP, Reeves C, Schmitt A, ''et al.'' |title=Somatic mutation of TSSC5, a novel imprinted gene from human chromosome 11p15.5. |journal=Cancer Res. |volume=58 |issue= 18 |pages= 4155–9 |year= 1998 |pmid= 9751628 |doi= }}
*{{cite journal | author=Lee MP |title=Somatic mutation of TSSC5, a novel imprinted gene from human chromosome 11p15.5 |journal=Cancer Res. |volume=58 |issue= 18 |pages= 4155–9 |year= 1998 |pmid= 9751628 |doi= | author2=Reeves C | author3=Schmitt A | display-authors=3 | last4=Su | first4=K | last5=Connors | first5=TD | last6=Hu | first6=RJ | last7=Brandenburg | first7=S | last8=Lee | first8=MJ | last9=Miller | first9=G }}
*{{cite journal | author=Morisaki H, Hatada I, Morisaki T, Mukai T |title=A novel gene, ITM, located between p57KIP2 and IPL, is imprinted in mice. |journal=DNA Res. |volume=5 |issue= 4 |pages= 235–40 |year= 1999 |pmid= 9802569 |doi=10.1093/dnares/5.4.235 }}
*{{cite journal | author=Morisaki H, Hatada I, Morisaki T, Mukai T |title=A novel gene, ITM, located between p57KIP2 and IPL, is imprinted in mice |journal=DNA Res. |volume=5 |issue= 4 |pages= 235–40 |year= 1999 |pmid= 9802569 |doi=10.1093/dnares/5.4.235 }}
*{{cite journal | author=Onyango P, Miller W, Lehoczky J, ''et al.'' |title=Sequence and comparative analysis of the mouse 1-megabase region orthologous to the human 11p15 imprinted domain. |journal=Genome Res. |volume=10 |issue= 11 |pages= 1697–710 |year= 2001 |pmid= 11076855 |doi=10.1101/gr.161800 }}
*{{cite journal | author=Onyango P |title=Sequence and comparative analysis of the mouse 1-megabase region orthologous to the human 11p15 imprinted domain |journal=Genome Res. |volume=10 |issue= 11 |pages= 1697–710 |year= 2001 |pmid= 11076855 |doi=10.1101/gr.161800 | author2=Miller W | author3=Lehoczky J | display-authors=3 | last4=Leung | first4=CT | last5=Birren | first5=B | last6=Wheelan | first6=S | last7=Dewar | first7=K | last8=Feinberg | first8=AP }}
*{{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 | pmc=139241 }}
*{{cite journal | author=Strausberg RL |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 | author2=Feingold EA | author3=Grouse LH | display-authors=3 | last4=Derge | first4=JG | last5=Klausner | first5=RD | last6=Collins | first6=FS | last7=Wagner | first7=L | last8=Shenmen | first8=CM | last9=Schuler | first9=GD }}
*{{cite journal | author=Gerhard DS, Wagner L, Feingold EA, ''et al.'' |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 | author=Gerhard DS |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 | author2=Wagner L | author3=Feingold EA | display-authors=3 | last4=Shenmen | first4=CM | last5=Grouse | first5=LH | last6=Schuler | first6=G | last7=Klein | first7=SL | last8=Old | first8=S | last9=Rasooly | first9=R }}
*{{cite journal | author=Yamada HY, Gorbsky GJ |title=Tumor suppressor candidate TSSC5 is regulated by UbcH6 and a novel ubiquitin ligase RING105. |journal=Oncogene |volume=25 |issue= 9 |pages= 1330–9 |year= 2006 |pmid= 16314844 |doi= 10.1038/sj.onc.1209167 | pmc=2713668 }}
*{{cite journal | author=Yamada HY, Gorbsky GJ |title=Tumor suppressor candidate TSSC5 is regulated by UbcH6 and a novel ubiquitin ligase RING105 |journal=Oncogene |volume=25 |issue= 9 |pages= 1330–9 |year= 2006 |pmid= 16314844 |doi= 10.1038/sj.onc.1209167 | pmc=2713668 }}
*{{cite journal | author=Gallagher E, Mc Goldrick A, Chung WY, ''et al.'' |title=Gain of imprinting of SLC22A18 sense and antisense transcripts in human breast cancer. |journal=Genomics |volume=88 |issue= 1 |pages= 12–7 |year= 2006 |pmid= 16624517 |doi= 10.1016/j.ygeno.2006.02.004 }}
*{{cite journal | author=Gallagher E |title=Gain of imprinting of SLC22A18 sense and antisense transcripts in human breast cancer |journal=Genomics |volume=88 |issue= 1 |pages= 12–7 |year= 2006 |pmid= 16624517 |doi= 10.1016/j.ygeno.2006.02.004 | author2=Mc Goldrick A | author3=Chung WY | display-authors=3 | last4=Mc Cormack | first4=O. | last5=Harrison | first5=M. | last6=Kerin | first6=M. | last7=Dervan | first7=P.A. | last8=Mc Cann | first8=A. }}
}}
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Revision as of 06:14, 19 June 2011

Template:PBB Solute carrier family 22 member 18 is a protein that in humans is encoded by the SLC22A18 gene.[1][2][3]

Template:PBB Summary

See also

References

  1. ^ Dao D, Frank D, Qian N, O'Keefe D, Vosatka RJ, Walsh CP, Tycko B (1998). "IMPT1, an imprinted gene similar to polyspecific transporter and multi-drug resistance genes". Hum Mol Genet. 7 (4): 597–608. doi:10.1093/hmg/7.4.597. PMID 9499412. {{cite journal}}: Unknown parameter |month= ignored (help)CS1 maint: multiple names: authors list (link)
  2. ^ Schwienbacher C, Sabbioni S, Campi M, Veronese A, Bernardi G, Menegatti A, Hatada I, Mukai T, Ohashi H, Barbanti-Brodano G, Croce CM, Negrini M (1998). "Transcriptional map of 170-kb region at chromosome 11p15.5: identification and mutational analysis of the BWR1A gene reveals the presence of mutations in tumor samples". Proc Natl Acad Sci U S A. 95 (7): 3873–8. doi:10.1073/pnas.95.7.3873. PMC 19930. PMID 9520460. {{cite journal}}: Unknown parameter |month= ignored (help)CS1 maint: multiple names: authors list (link)
  3. ^ "Entrez Gene: SLC22A18 solute carrier family 22 (organic cation transporter), member 18".

Further reading

Template:PBB Further reading

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