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- Publisher Website: 10.1038/sj.onc.1201970
- Scopus: eid_2-s2.0-0032490839
- PMID: 9704933
- WOS: WOS:000075195300015
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Article: Sex difference in immunostaining of RET in the adult mouse kidney
Title | Sex difference in immunostaining of RET in the adult mouse kidney |
---|---|
Authors | |
Keywords | c-ret Kidney RET |
Issue Date | 1998 |
Publisher | Nature Publishing Group. The Journal's web site is located at http://www.nature.com/onc |
Citation | Oncogene, 1998, v. 17 n. 5, p. 661-666 How to Cite? |
Abstract | The c-ret proto-oncogene encodes a receptor tyrosine kinase which is important for the development of the kidney and the enteric nervous system. During nephrogenesis, c-ret is expressed in the ureteric bud epithelium and later in its derivative, the collecting duct. This takes place during 11-17.5 days post-coitum (d.p.c.) in the mouse and our immunohistochemical study showed that the RET protein co-localized with the transcript. At 18.5 d.p.c. the kidney is fully differentiated. At 18.5 d.p.c., 1 week and 10 weeks old, RET was found in the proximal convoluted tubules, which is formed from the condensed mesenchyme. This suggests that c-ret may also play a role in kidney function. For the 10 weeks old kidney, RET immunostaining in male was concentrated on the basolateral side while female had a stronger staining in the whole cell. Furthermore, cytoplasmic staining was observed in male whereas both cytoplasmic and nuclear staining was found in female. c-ret transcript was detected by RT-PCR, and in situ hybridization showed its expression throughout the kidney. The reason for the sex-specific staining and the role of RET in kidney function remain to be determined. |
Persistent Identifier | http://hdl.handle.net/10722/49266 |
ISSN | 2023 Impact Factor: 6.9 2023 SCImago Journal Rankings: 2.334 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Chan, SY | en_HK |
dc.contributor.author | Lee, DCW | en_HK |
dc.date.accessioned | 2008-06-12T06:38:01Z | - |
dc.date.available | 2008-06-12T06:38:01Z | - |
dc.date.issued | 1998 | en_HK |
dc.identifier.citation | Oncogene, 1998, v. 17 n. 5, p. 661-666 | en_HK |
dc.identifier.issn | 0950-9232 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/49266 | - |
dc.description.abstract | The c-ret proto-oncogene encodes a receptor tyrosine kinase which is important for the development of the kidney and the enteric nervous system. During nephrogenesis, c-ret is expressed in the ureteric bud epithelium and later in its derivative, the collecting duct. This takes place during 11-17.5 days post-coitum (d.p.c.) in the mouse and our immunohistochemical study showed that the RET protein co-localized with the transcript. At 18.5 d.p.c. the kidney is fully differentiated. At 18.5 d.p.c., 1 week and 10 weeks old, RET was found in the proximal convoluted tubules, which is formed from the condensed mesenchyme. This suggests that c-ret may also play a role in kidney function. For the 10 weeks old kidney, RET immunostaining in male was concentrated on the basolateral side while female had a stronger staining in the whole cell. Furthermore, cytoplasmic staining was observed in male whereas both cytoplasmic and nuclear staining was found in female. c-ret transcript was detected by RT-PCR, and in situ hybridization showed its expression throughout the kidney. The reason for the sex-specific staining and the role of RET in kidney function remain to be determined. | en_HK |
dc.format.extent | 418 bytes | - |
dc.format.mimetype | text/html | - |
dc.language | eng | en_HK |
dc.publisher | Nature Publishing Group. The Journal's web site is located at http://www.nature.com/onc | en_HK |
dc.relation.ispartof | Oncogene | en_HK |
dc.subject | c-ret | en_HK |
dc.subject | Kidney | en_HK |
dc.subject | RET | en_HK |
dc.title | Sex difference in immunostaining of RET in the adult mouse kidney | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Chan, SY:sychan@hkucc.hku.hk | en_HK |
dc.identifier.authority | Chan, SY=rp00356 | en_HK |
dc.description.nature | link_to_OA_fulltext | en_HK |
dc.identifier.doi | 10.1038/sj.onc.1201970 | en_HK |
dc.identifier.pmid | 9704933 | - |
dc.identifier.scopus | eid_2-s2.0-0032490839 | en_HK |
dc.identifier.hkuros | 38777 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-0032490839&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 17 | en_HK |
dc.identifier.issue | 5 | en_HK |
dc.identifier.spage | 661 | en_HK |
dc.identifier.epage | 666 | en_HK |
dc.identifier.isi | WOS:000075195300015 | - |
dc.publisher.place | United Kingdom | en_HK |
dc.identifier.scopusauthorid | Chan, SY=7404255082 | en_HK |
dc.identifier.scopusauthorid | Lee, DCW=7406663288 | en_HK |
dc.identifier.issnl | 0950-9232 | - |