偽體染色體區 (Chinese Wikipedia)

Analysis of information sources in references of the Wikipedia article "偽體染色體區" in Chinese language version.

refsWebsite

Global rank Chinese rank

22nih.gov

4^th place

5^th place

14doi.org

2^nd place

23^rd place

11web.archive.org

1^st place

2genenames.org

low place

2worldcat.org

5^th place

12^th place

1oxfordjournals.org

1,389^th place

860^th place

1genome.org

low place

1biomedcentral.com

2,747^th place

1,988^th place

1jbc.org

4,455^th place

2,125^th place

1jimmunol.org

low place

1e-emm.org

low place

1elsevier.com

610^th place

388^th place

1scielo.br

1,606^th place

2,599^th place

biomedcentral.com

Levy MA, Fernandes AD, Tremblay DC, Seah C, Bérubé NG. The SWI/SNF protein ATRX co-regulates pseudoautosomal genes that have translocated to autosomes in the mouse genome. BMC Genomics. 2008, 9: 468 [2011-02-18]. PMC 2577121 . PMID 18842153. doi:10.1186/1471-2164-9-468. （原始内容存档于2011-05-25）.

doi.org

Helena Mangs A, Morris BJ. The Human Pseudoautosomal Region (PAR): Origin, Function and Future. Curr. Genomics. April 2007, 8 (2): 129–36. PMC 2435358 . PMID 18660847. doi:10.2174/138920207780368141.
Blaschke RJ, Rappold G. The pseudoautosomal regions, SHOX and disease. Curr Opin Genet Dev. 2006, 16 (3): 233–9. PMID 16650979. doi:10.1016/j.gde.2006.04.004.
Ciccodicola A, D'Esposito M, Esposito T; et al. Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal region. Hum. Mol. Genet. February 2000, 9 (3): 395–401 [2011-02-18]. PMID 10655549. doi:10.1093/hmg/9.3.395. （原始内容存档于2019-09-15）.
Charchar FJ, Svartman M, El-Mogharbel N; et al. Complex events in the evolution of the human pseudoautosomal region 2 (PAR2). Genome Res. February 2003, 13 (2): 281–6 [2011-02-18]. PMC 420362 . PMID 12566406. doi:10.1101/gr.390503. （原始内容存档于2019-09-15）.
Levy MA, Fernandes AD, Tremblay DC, Seah C, Bérubé NG. The SWI/SNF protein ATRX co-regulates pseudoautosomal genes that have translocated to autosomes in the mouse genome. BMC Genomics. 2008, 9: 468 [2011-02-18]. PMC 2577121 . PMID 18842153. doi:10.1186/1471-2164-9-468. （原始内容存档于2011-05-25）.
Ried K, Rao E, Schiebel K, Rappold GA. Gene duplications as a recurrent theme in the evolution of the human pseudoautosomal region 1: isolation of the gene ASMTL. Hum Mol Genet. Dec 1998, 7 (11): 1771–8. PMID 9736779. doi:10.1093/hmg/7.11.1771.
Bernard G, Raimondi V, Alberti I, Pourtein M, Widjenes J, Ticchioni M, Bernard A. CD99 (E2) up-regulates alpha4beta1-dependent T cell adhesion to inflamed vascular endothelium under flow conditions. European journal of immunology. October 2000, 30 (10): 3061–5. PMID 11069091. doi:10.1002/1521-4141(200010)30:10<3061::AID-IMMU3061>3.0.CO;2-M.
Nicola NA, Metcalf D. Binding of ¹²⁵I-labeled granulocyte colony-stimulating factor to normal murine hemopoietic cells. J. Cell. Physiol. 1985, 124 (2): 313–21. PMID 3876343. doi:10.1002/jcp.1041240222.
Persson B, Kallberg Y, Bray JE, Bruford E, Dellaporta SL, Favia AD, Duarte RG, Jörnvall H, Kavanagh KL, Kedishvili N, Kisiela M, Maser E, Mindnich R, Orchard S, Penning TM, Thornton JM, Adamski J, Oppermann U. The SDR (short-chain dehydrogenase/reductase and related enzymes) nomenclature initiative. Chem. Biol. Interact. November 2008, 178 (1-3): 94–8. PMC 2896744 . PMID 19027726. doi:10.1016/j.cbi.2008.10.040.
Vawter MP, Harvey PD, DeLisi LE. Dysregulation of X-linked gene expression in Klinefelter's syndrome and association with verbal cognition. Am. J. Med. Genet. B Neuropsychiatr. Genet. September 2007, 144B (6): 728–34. PMC 2094046 . PMID 17347996. doi:10.1002/ajmg.b.30454.
Skaletsky H, Kuroda-Kawaguchi T, Minx PJ; et al. The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes. Nature. June 2003, 423 (6942): 825–37. PMID 12815422. doi:10.1038/nature01722.
Palmieri F. The mitochondrial transporter family (SLC25): physiological and pathological implications. Pflugers Arch. February 2004, 447 (5): 689–709. PMID 14598172. doi:10.1007/s00424-003-1099-7.
Tippett P, Ellis NA. The Xg blood group system: a review. Transfus Med Rev. October 1998, 12 (4): 233–57 [2011-02-18]. PMID 9798268. doi:10.1016/S0887-7963(98)80001-1. （原始内容存档于2020-07-28）.
Renata de Lima1; Cristina Forti Iamada; Luciana Oliveira Silva; Maricilda Palandi de Mello; Andréa Trevas Maciel-Guerra. An illustrative case of Léri-Weill dyschondrosteosis. Centro de Biologia Molecular e Engenharia Genética, Universidade Estadual de Campinas, Campinas, SP, Brazil; Departamento de Genética Médica, Faculdade de Ciências Médicas, Universidade Estadual de Campinas, Campinas, SP, Brazil; Departamento de Pediatria, Faculdade de Ciências Médicas, Universidade Estadual de Campinas, Campinas, SP, Brazil. 2008-11-19 [2011-02-18]. ISSN 1415-4757. doi:10.1590/S1415-47572008005000017. （原始内容存档于2017-12-02）（英语）.

e-emm.org

Oh KI, Kim BK, Ban YL, Choi EY, Jung KC, Lee IS, Park SH. CD99 activates T cells via a costimulatory function that promotes raft association of TCR complex and tyrosine phosphorylation of TCR zeta. Experimental & molecular medicine. April 2007, 39 (2): 176–84 [2011年2月18日]. PMID 17464179. （原始内容存档于2011年7月26日）.

elsevier.com

linkinghub.elsevier.com

Tippett P, Ellis NA. The Xg blood group system: a review. Transfus Med Rev. October 1998, 12 (4): 233–57 [2011-02-18]. PMID 9798268. doi:10.1016/S0887-7963(98)80001-1. （原始内容存档于2020-07-28）.

genenames.org

Pseudoautosomal regions Gene Family. HUGO Gene Nomenclature Committee. [2017-05-11]. （原始内容存档于2017-07-11）.
WASH6P. [2009-01-05]. （原始内容存档于2012-10-24）.

genome.org

Charchar FJ, Svartman M, El-Mogharbel N; et al. Complex events in the evolution of the human pseudoautosomal region 2 (PAR2). Genome Res. February 2003, 13 (2): 281–6 [2011-02-18]. PMC 420362 . PMID 12566406. doi:10.1101/gr.390503. （原始内容存档于2019-09-15）.

jbc.org

Rodriguez IR, Mazuruk K, Schoen TJ, Chader GJ. Structural analysis of the human hydroxyindole-O-methyltransferase gene. Presence of two distinct promoters. J. Biol. Chem. December 1994, 269 (50): 31969–77 [2011-02-18]. PMID 7989373. （原始内容存档于2003-10-04）.

jimmunol.org

Bernard G, Breittmayer JP, de Matteis M, Trampont P, Hofman P, Senik A, Bernard A. Apoptosis of immature thymocytes mediated by E2/CD99. Journal of immunology (Baltimore, Md. : 1950). March 1997, 158 (6): 2543–50. PMID 9058785.

nih.gov

ncbi.nlm.nih.gov

Helena Mangs A, Morris BJ. The Human Pseudoautosomal Region (PAR): Origin, Function and Future. Curr. Genomics. April 2007, 8 (2): 129–36. PMC 2435358 . PMID 18660847. doi:10.2174/138920207780368141.
Blaschke RJ, Rappold G. The pseudoautosomal regions, SHOX and disease. Curr Opin Genet Dev. 2006, 16 (3): 233–9. PMID 16650979. doi:10.1016/j.gde.2006.04.004.
Ciccodicola A, D'Esposito M, Esposito T; et al. Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal region. Hum. Mol. Genet. February 2000, 9 (3): 395–401 [2011-02-18]. PMID 10655549. doi:10.1093/hmg/9.3.395. （原始内容存档于2019-09-15）.
Genome Reference Consortium. Human genome overview GRCh38.p10. 2017-01-06 [2017-05-10]. （原始内容存档于2016-10-09）.
Charchar FJ, Svartman M, El-Mogharbel N; et al. Complex events in the evolution of the human pseudoautosomal region 2 (PAR2). Genome Res. February 2003, 13 (2): 281–6 [2011-02-18]. PMC 420362 . PMID 12566406. doi:10.1101/gr.390503. （原始内容存档于2019-09-15）.
Levy MA, Fernandes AD, Tremblay DC, Seah C, Bérubé NG. The SWI/SNF protein ATRX co-regulates pseudoautosomal genes that have translocated to autosomes in the mouse genome. BMC Genomics. 2008, 9: 468 [2011-02-18]. PMC 2577121 . PMID 18842153. doi:10.1186/1471-2164-9-468. （原始内容存档于2011-05-25）.
Rodriguez IR, Mazuruk K, Schoen TJ, Chader GJ. Structural analysis of the human hydroxyindole-O-methyltransferase gene. Presence of two distinct promoters. J. Biol. Chem. December 1994, 269 (50): 31969–77 [2011-02-18]. PMID 7989373. （原始内容存档于2003-10-04）.
Ried K, Rao E, Schiebel K, Rappold GA. Gene duplications as a recurrent theme in the evolution of the human pseudoautosomal region 1: isolation of the gene ASMTL. Hum Mol Genet. Dec 1998, 7 (11): 1771–8. PMID 9736779. doi:10.1093/hmg/7.11.1771.
Bernard G, Raimondi V, Alberti I, Pourtein M, Widjenes J, Ticchioni M, Bernard A. CD99 (E2) up-regulates alpha4beta1-dependent T cell adhesion to inflamed vascular endothelium under flow conditions. European journal of immunology. October 2000, 30 (10): 3061–5. PMID 11069091. doi:10.1002/1521-4141(200010)30:10<3061::AID-IMMU3061>3.0.CO;2-M.
Bernard G, Breittmayer JP, de Matteis M, Trampont P, Hofman P, Senik A, Bernard A. Apoptosis of immature thymocytes mediated by E2/CD99. Journal of immunology (Baltimore, Md. : 1950). March 1997, 158 (6): 2543–50. PMID 9058785.
Oh KI, Kim BK, Ban YL, Choi EY, Jung KC, Lee IS, Park SH. CD99 activates T cells via a costimulatory function that promotes raft association of TCR complex and tyrosine phosphorylation of TCR zeta. Experimental & molecular medicine. April 2007, 39 (2): 176–84 [2011年2月18日]. PMID 17464179. （原始内容存档于2011年7月26日）.
Entrez Gene: CRLF2 cytokine receptor-like factor 2.
Nicola NA, Metcalf D. Binding of ¹²⁵I-labeled granulocyte colony-stimulating factor to normal murine hemopoietic cells. J. Cell. Physiol. 1985, 124 (2): 313–21. PMID 3876343. doi:10.1002/jcp.1041240222.
Persson B, Kallberg Y, Bray JE, Bruford E, Dellaporta SL, Favia AD, Duarte RG, Jörnvall H, Kavanagh KL, Kedishvili N, Kisiela M, Maser E, Mindnich R, Orchard S, Penning TM, Thornton JM, Adamski J, Oppermann U. The SDR (short-chain dehydrogenase/reductase and related enzymes) nomenclature initiative. Chem. Biol. Interact. November 2008, 178 (1-3): 94–8. PMC 2896744 . PMID 19027726. doi:10.1016/j.cbi.2008.10.040.
Vawter MP, Harvey PD, DeLisi LE. Dysregulation of X-linked gene expression in Klinefelter's syndrome and association with verbal cognition. Am. J. Med. Genet. B Neuropsychiatr. Genet. September 2007, 144B (6): 728–34. PMC 2094046 . PMID 17347996. doi:10.1002/ajmg.b.30454.
Stomski, F C; Sun Q, Bagley C J, Woodcock J, Goodall G, Andrews R K, Berndt M C, Lopez A F. Human interleukin-3 (IL-3) induces disulfide-linked IL-3 receptor alpha- and beta-chain heterodimerization, which is required for receptor activation but not high-affinity binding. Mol. Cell. Biol. (UNITED STATES). Jun 1996, 16 (6): 3035–46. ISSN 0270-7306. PMC 231298 . PMID 8649415.
Entrez Gene: P2RY8 purinergic receptor P2Y, G-protein coupled, 8.
Skaletsky H, Kuroda-Kawaguchi T, Minx PJ; et al. The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes. Nature. June 2003, 423 (6942): 825–37. PMID 12815422. doi:10.1038/nature01722.
Entrez Gene: PPP2R3B protein phosphatase 2 (formerly 2A), regulatory subunit B, beta.
Palmieri F. The mitochondrial transporter family (SLC25): physiological and pathological implications. Pflugers Arch. February 2004, 447 (5): 689–709. PMID 14598172. doi:10.1007/s00424-003-1099-7.
Tippett P, Ellis NA. The Xg blood group system: a review. Transfus Med Rev. October 1998, 12 (4): 233–57 [2011-02-18]. PMID 9798268. doi:10.1016/S0887-7963(98)80001-1. （原始内容存档于2020-07-28）.

ghr.nlm.nih.gov

SHOX - short stature homeobox - Genetics Home Reference. U.S. National Library of Medicine. [2008-02-18 date = 2005-09-01]. （原始内容存档于2007-10-12）.

oxfordjournals.org

hmg.oxfordjournals.org

Ciccodicola A, D'Esposito M, Esposito T; et al. Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal region. Hum. Mol. Genet. February 2000, 9 (3): 395–401 [2011-02-18]. PMID 10655549. doi:10.1093/hmg/9.3.395. （原始内容存档于2019-09-15）.

scielo.br

Renata de Lima1; Cristina Forti Iamada; Luciana Oliveira Silva; Maricilda Palandi de Mello; Andréa Trevas Maciel-Guerra. An illustrative case of Léri-Weill dyschondrosteosis. Centro de Biologia Molecular e Engenharia Genética, Universidade Estadual de Campinas, Campinas, SP, Brazil; Departamento de Genética Médica, Faculdade de Ciências Médicas, Universidade Estadual de Campinas, Campinas, SP, Brazil; Departamento de Pediatria, Faculdade de Ciências Médicas, Universidade Estadual de Campinas, Campinas, SP, Brazil. 2008-11-19 [2011-02-18]. ISSN 1415-4757. doi:10.1590/S1415-47572008005000017. （原始内容存档于2017-12-02）（英语）.

web.archive.org

Ciccodicola A, D'Esposito M, Esposito T; et al. Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal region. Hum. Mol. Genet. February 2000, 9 (3): 395–401 [2011-02-18]. PMID 10655549. doi:10.1093/hmg/9.3.395. （原始内容存档于2019-09-15）.
Genome Reference Consortium. Human genome overview GRCh38.p10. 2017-01-06 [2017-05-10]. （原始内容存档于2016-10-09）.
Pseudoautosomal regions Gene Family. HUGO Gene Nomenclature Committee. [2017-05-11]. （原始内容存档于2017-07-11）.
Charchar FJ, Svartman M, El-Mogharbel N; et al. Complex events in the evolution of the human pseudoautosomal region 2 (PAR2). Genome Res. February 2003, 13 (2): 281–6 [2011-02-18]. PMC 420362 . PMID 12566406. doi:10.1101/gr.390503. （原始内容存档于2019-09-15）.
Levy MA, Fernandes AD, Tremblay DC, Seah C, Bérubé NG. The SWI/SNF protein ATRX co-regulates pseudoautosomal genes that have translocated to autosomes in the mouse genome. BMC Genomics. 2008, 9: 468 [2011-02-18]. PMC 2577121 . PMID 18842153. doi:10.1186/1471-2164-9-468. （原始内容存档于2011-05-25）.
Rodriguez IR, Mazuruk K, Schoen TJ, Chader GJ. Structural analysis of the human hydroxyindole-O-methyltransferase gene. Presence of two distinct promoters. J. Biol. Chem. December 1994, 269 (50): 31969–77 [2011-02-18]. PMID 7989373. （原始内容存档于2003-10-04）.
Oh KI, Kim BK, Ban YL, Choi EY, Jung KC, Lee IS, Park SH. CD99 activates T cells via a costimulatory function that promotes raft association of TCR complex and tyrosine phosphorylation of TCR zeta. Experimental & molecular medicine. April 2007, 39 (2): 176–84 [2011年2月18日]. PMID 17464179. （原始内容存档于2011年7月26日）.
SHOX - short stature homeobox - Genetics Home Reference. U.S. National Library of Medicine. [2008-02-18 date = 2005-09-01]. （原始内容存档于2007-10-12）.
Tippett P, Ellis NA. The Xg blood group system: a review. Transfus Med Rev. October 1998, 12 (4): 233–57 [2011-02-18]. PMID 9798268. doi:10.1016/S0887-7963(98)80001-1. （原始内容存档于2020-07-28）.
WASH6P. [2009-01-05]. （原始内容存档于2012-10-24）.
Renata de Lima1; Cristina Forti Iamada; Luciana Oliveira Silva; Maricilda Palandi de Mello; Andréa Trevas Maciel-Guerra. An illustrative case of Léri-Weill dyschondrosteosis. Centro de Biologia Molecular e Engenharia Genética, Universidade Estadual de Campinas, Campinas, SP, Brazil; Departamento de Genética Médica, Faculdade de Ciências Médicas, Universidade Estadual de Campinas, Campinas, SP, Brazil; Departamento de Pediatria, Faculdade de Ciências Médicas, Universidade Estadual de Campinas, Campinas, SP, Brazil. 2008-11-19 [2011-02-18]. ISSN 1415-4757. doi:10.1590/S1415-47572008005000017. （原始内容存档于2017-12-02）（英语）.

worldcat.org

Stomski, F C; Sun Q, Bagley C J, Woodcock J, Goodall G, Andrews R K, Berndt M C, Lopez A F. Human interleukin-3 (IL-3) induces disulfide-linked IL-3 receptor alpha- and beta-chain heterodimerization, which is required for receptor activation but not high-affinity binding. Mol. Cell. Biol. (UNITED STATES). Jun 1996, 16 (6): 3035–46. ISSN 0270-7306. PMC 231298 . PMID 8649415.
Renata de Lima1; Cristina Forti Iamada; Luciana Oliveira Silva; Maricilda Palandi de Mello; Andréa Trevas Maciel-Guerra. An illustrative case of Léri-Weill dyschondrosteosis. Centro de Biologia Molecular e Engenharia Genética, Universidade Estadual de Campinas, Campinas, SP, Brazil; Departamento de Genética Médica, Faculdade de Ciências Médicas, Universidade Estadual de Campinas, Campinas, SP, Brazil; Departamento de Pediatria, Faculdade de Ciências Médicas, Universidade Estadual de Campinas, Campinas, SP, Brazil. 2008-11-19 [2011-02-18]. ISSN 1415-4757. doi:10.1590/S1415-47572008005000017. （原始内容存档于2017-12-02）（英语）.