偽常染色体領域 (Japanese Wikipedia)

Analysis of information sources in references of the Wikipedia article "偽常染色体領域" in Japanese language version.

refsWebsite

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17nih.gov

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24^th place

10doi.org

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6^th place

4genenames.org

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doi.org

Mangs, Helena; Morris BJ (2007). “The Human Pseudoautosomal Region (PAR): Origin, Function and Future.”. Current Genomics 8 (2): 129–136. doi:10.2174/138920207780368141. PMC 2435358. PMID 18660847.
“The pseudoautosomal regions, SHOX and disease”. Curr Opin Genet Dev 16 (3): 233–9. (2006). doi:10.1016/j.gde.2006.04.004. PMID 16650979.
“The Human Pseudoautosomal Region (PAR): Origin, Function and Future”. Curr. Genomics 8 (2): 129–36. (April 2007). doi:10.2174/138920207780368141. PMC 2435358. PMID 18660847.
“Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal region”. Hum. Mol. Genet. 9 (3): 395–401. (February 2000). doi:10.1093/hmg/9.3.395. PMID 10655549.
“Sex chromosome loss and the pseudoautosomal region genes in hematological malignancies”. Oncotarget 7 (44): 72356–72372. (2016). doi:10.18632/oncotarget.12050. PMC 5342167. PMID 27655702.
“Complex events in the evolution of the human pseudoautosomal region 2 (PAR2)”. Genome Res. 13 (2): 281–6. (February 2003). doi:10.1101/gr.390503. PMC 420362. PMID 12566406.
“The SWI/SNF protein ATRX co-regulates pseudoautosomal genes that have translocated to autosomes in the mouse genome”. BMC Genomics 9: 468. (2008). doi:10.1186/1471-2164-9-468. PMC 2577121. PMID 18842153.
Eichner, E.M. (February 1991). “The mouse Y* chromosome involves a complex rearrangement including interstitial positioning of the Y-pseudoautosomal region”. Cytogenetics and Cell Genetics 57 (4): 221–230. doi:10.1159/000133152. PMID 1743079.
“The pseudoautosomal regions, SHOX and disease”. Curr. Opin. Genet. Dev. 16 (3): 233–9. (June 2006). doi:10.1016/j.gde.2006.04.004. PMID 16650979.
“A novel class of Pseudoautosomal region 1 deletions downstream of SHOX is associated with Leri-Weill dyschondrosteosis”. Am. J. Hum. Genet. 77 (4): 533–44. (October 2005). doi:10.1086/449313. PMC 1275603. PMID 16175500.

genenames.org

“Pseudoautosomal regions Gene Family”. HUGO Gene Nomenclature Committee. 2017年5月11日閲覧。
“Pseudoautosomal region 1 (PAR1) Gene Family”. HUGO Gene Nomenclature Committee. 2017年5月12日閲覧。
“Pseudoautosomal region 2 (PAR2) Gene group”. HUGO Gene Nomenclature Committee. 2019年8月30日閲覧。
“WASH6P”. HUGO Gene Nomenclature Committee. 2019年8月30日閲覧。

nih.gov

pubmed.ncbi.nlm.nih.gov

Mangs, Helena; Morris BJ (2007). “The Human Pseudoautosomal Region (PAR): Origin, Function and Future.”. Current Genomics 8 (2): 129–136. doi:10.2174/138920207780368141. PMC 2435358. PMID 18660847.
“The pseudoautosomal regions, SHOX and disease”. Curr Opin Genet Dev 16 (3): 233–9. (2006). doi:10.1016/j.gde.2006.04.004. PMID 16650979.
“The Human Pseudoautosomal Region (PAR): Origin, Function and Future”. Curr. Genomics 8 (2): 129–36. (April 2007). doi:10.2174/138920207780368141. PMC 2435358. PMID 18660847.
“Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal region”. Hum. Mol. Genet. 9 (3): 395–401. (February 2000). doi:10.1093/hmg/9.3.395. PMID 10655549.
“Sex chromosome loss and the pseudoautosomal region genes in hematological malignancies”. Oncotarget 7 (44): 72356–72372. (2016). doi:10.18632/oncotarget.12050. PMC 5342167. PMID 27655702.
“Complex events in the evolution of the human pseudoautosomal region 2 (PAR2)”. Genome Res. 13 (2): 281–6. (February 2003). doi:10.1101/gr.390503. PMC 420362. PMID 12566406.
“The SWI/SNF protein ATRX co-regulates pseudoautosomal genes that have translocated to autosomes in the mouse genome”. BMC Genomics 9: 468. (2008). doi:10.1186/1471-2164-9-468. PMC 2577121. PMID 18842153.
Eichner, E.M. (February 1991). “The mouse Y* chromosome involves a complex rearrangement including interstitial positioning of the Y-pseudoautosomal region”. Cytogenetics and Cell Genetics 57 (4): 221–230. doi:10.1159/000133152. PMID 1743079.
“The pseudoautosomal regions, SHOX and disease”. Curr. Opin. Genet. Dev. 16 (3): 233–9. (June 2006). doi:10.1016/j.gde.2006.04.004. PMID 16650979.
“A novel class of Pseudoautosomal region 1 deletions downstream of SHOX is associated with Leri-Weill dyschondrosteosis”. Am. J. Hum. Genet. 77 (4): 533–44. (October 2005). doi:10.1086/449313. PMC 1275603. PMID 16175500.