FOXP3 (Ukrainian Wikipedia)

Analysis of information sources in references of the Wikipedia article "FOXP3" in Ukrainian language version.

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17nih.gov

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11doi.org

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2web.archive.org

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1wikidata.org

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1genenames.org

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1uniprot.org

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archive.org

Bennett CL, Yoshioka R, Kiyosawa H, Barker DF, Fain PR, Shigeoka AO, Chance PF (February 2000). X-Linked syndrome of polyendocrinopathy, immune dysfunction, and diarrhea maps to Xp11.23-Xq13.3. Am. J. Hum. Genet. 66 (2): 461—468. doi:10.1086/302761. PMC 1288099. PMID 10677306.

doi.org

Zhang L, Zhao Y (June 2007). The regulation of Foxp3 expression in regulatory CD4(+)CD25(+)T cells: multiple pathways on the road. J. Cell. Physiol. 211 (3): 590—597. doi:10.1002/jcp.21001. PMID 17311282.
Marson A, Kretschmer K, Frampton GM, Jacobsen ES, Polansky JK, MacIsaac KD, Levine SS, Fraenkel E, von Boehmer H, Young RA (February 2007). Foxp3 occupancy and regulation of key target genes during T-cell stimulation. Nature. 445 (7130): 931—5. doi:10.1038/nature05478. PMC 3008159. PMID 17237765.
Bennett CL, Yoshioka R, Kiyosawa H, Barker DF, Fain PR, Shigeoka AO, Chance PF (February 2000). X-Linked syndrome of polyendocrinopathy, immune dysfunction, and diarrhea maps to Xp11.23-Xq13.3. Am. J. Hum. Genet. 66 (2): 461—468. doi:10.1086/302761. PMC 1288099. PMID 10677306.
Brunkow ME, Jeffery EW, Hjerrild KA, Paeper B, Clark LB, Yasayko SA, Wilkinson JE, Galas D, Ziegler SF, Ramsdell F (January 2001). Disruption of a new forkhead/winged-helix protein, scurfin, results in the fatal lymphoproliferative disorder of the scurfy mouse. Nat. Genet. 27 (1): 68—73. doi:10.1038/83784. PMID 11138001.
Hori S, Nomura T, Sakaguchi S (February 2003). Control of regulatory T cell development by the transcription factor Foxp3. Science. 299 (5609): 1057—61. doi:10.1126/science.1079490. PMID 12522256.
Fontenot JD, Gavin MA, Rudensky AY (April 2003). Foxp3 programs the development and function of CD4+CD25+ regulatory T cells. Nat. Immunol. 4 (4): 330—6. doi:10.1038/ni904. PMID 12612578.
Fontenot JD, Rasmussen JP, Williams LM, Dooley JL, Farr AG, Rudensky AY (March 2005). Regulatory T cell lineage specification by the forkhead transcription factor foxp3. Immunity. 22 (3): 329—41. doi:10.1016/j.immuni.2005.01.016. PMID 15780990.
Suri-Payer E, Fritzsching B (August 2006). Regulatory T cells in experimental autoimmune disease. Springer Semin. Immunopathol. 28 (1): 3—16. doi:10.1007/s00281-006-0021-8. PMID 16838180.
Beyer M, Schultze JL (August 2006). Regulatory T cells in cancer. Blood. 108 (3): 804—11. doi:10.1182/blood-2006-02-002774. PMID 16861339.
Alvarado-Sánchez B, Hernández-Castro B, Portales-Pérez D, Baranda L, Layseca-Espinosa E, Abud-Mendoza C, Cubillas-Tejeda AC, González-Amaro R (September 2006). Regulatory T cells in patients with systemic lupus erythematosus. J. Autoimmun. 27 (2): 110—8. doi:10.1016/j.jaut.2006.06.005. PMID 16890406.
Bennett CL, Christie J, Ramsdell F, Brunkow ME, Ferguson PJ, Whitesell L, Kelly TE, Saulsbury FT, Chance PF, Ochs HD (January 2001). The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3. Nat. Genet. 27 (1): 20—1. doi:10.1038/83713. PMID 11137993.

genenames.org

HUGO Gene Nomenclature Commitee, HGNC:6106 (англ.) . Архів оригіналу за 13 лютого 2018. Процитовано 12 лютого 2018. [Архівовано 2018-02-13 у Wayback Machine.]

nih.gov

pubmed.ncbi.nlm.nih.gov

Zhang L, Zhao Y (June 2007). The regulation of Foxp3 expression in regulatory CD4(+)CD25(+)T cells: multiple pathways on the road. J. Cell. Physiol. 211 (3): 590—597. doi:10.1002/jcp.21001. PMID 17311282.
Marson A, Kretschmer K, Frampton GM, Jacobsen ES, Polansky JK, MacIsaac KD, Levine SS, Fraenkel E, von Boehmer H, Young RA (February 2007). Foxp3 occupancy and regulation of key target genes during T-cell stimulation. Nature. 445 (7130): 931—5. doi:10.1038/nature05478. PMC 3008159. PMID 17237765.
Bennett CL, Yoshioka R, Kiyosawa H, Barker DF, Fain PR, Shigeoka AO, Chance PF (February 2000). X-Linked syndrome of polyendocrinopathy, immune dysfunction, and diarrhea maps to Xp11.23-Xq13.3. Am. J. Hum. Genet. 66 (2): 461—468. doi:10.1086/302761. PMC 1288099. PMID 10677306.
Brunkow ME, Jeffery EW, Hjerrild KA, Paeper B, Clark LB, Yasayko SA, Wilkinson JE, Galas D, Ziegler SF, Ramsdell F (January 2001). Disruption of a new forkhead/winged-helix protein, scurfin, results in the fatal lymphoproliferative disorder of the scurfy mouse. Nat. Genet. 27 (1): 68—73. doi:10.1038/83784. PMID 11138001.
Hori S, Nomura T, Sakaguchi S (February 2003). Control of regulatory T cell development by the transcription factor Foxp3. Science. 299 (5609): 1057—61. doi:10.1126/science.1079490. PMID 12522256.
Fontenot JD, Gavin MA, Rudensky AY (April 2003). Foxp3 programs the development and function of CD4+CD25+ regulatory T cells. Nat. Immunol. 4 (4): 330—6. doi:10.1038/ni904. PMID 12612578.
Fontenot JD, Rasmussen JP, Williams LM, Dooley JL, Farr AG, Rudensky AY (March 2005). Regulatory T cell lineage specification by the forkhead transcription factor foxp3. Immunity. 22 (3): 329—41. doi:10.1016/j.immuni.2005.01.016. PMID 15780990.
Suri-Payer E, Fritzsching B (August 2006). Regulatory T cells in experimental autoimmune disease. Springer Semin. Immunopathol. 28 (1): 3—16. doi:10.1007/s00281-006-0021-8. PMID 16838180.
Beyer M, Schultze JL (August 2006). Regulatory T cells in cancer. Blood. 108 (3): 804—11. doi:10.1182/blood-2006-02-002774. PMID 16861339.
Alvarado-Sánchez B, Hernández-Castro B, Portales-Pérez D, Baranda L, Layseca-Espinosa E, Abud-Mendoza C, Cubillas-Tejeda AC, González-Amaro R (September 2006). Regulatory T cells in patients with systemic lupus erythematosus. J. Autoimmun. 27 (2): 110—8. doi:10.1016/j.jaut.2006.06.005. PMID 16890406.
Bennett CL, Christie J, Ramsdell F, Brunkow ME, Ferguson PJ, Whitesell L, Kelly TE, Saulsbury FT, Chance PF, Ochs HD (January 2001). The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3. Nat. Genet. 27 (1): 20—1. doi:10.1038/83713. PMID 11137993.
Tan B, Anaka M, Deb S, Freyer C, Ebert LM, Chueh AC, Al-Obaidi S, Behren A, Jayachandran A, Cebon J, Chen W, Mariadason JM (20 грудня 2013). FOXP3 over-expression inhibits melanoma tumorigenesis via effects on proliferation and apoptosis. Oncotarget. 5 (1): 264—76. PMC 3960207. PMID 24406338.

ncbi.nlm.nih.gov

Human PubMed Reference:.
Mouse PubMed Reference:.
Marson A, Kretschmer K, Frampton GM, Jacobsen ES, Polansky JK, MacIsaac KD, Levine SS, Fraenkel E, von Boehmer H, Young RA (February 2007). Foxp3 occupancy and regulation of key target genes during T-cell stimulation. Nature. 445 (7130): 931—5. doi:10.1038/nature05478. PMC 3008159. PMID 17237765.
Bennett CL, Yoshioka R, Kiyosawa H, Barker DF, Fain PR, Shigeoka AO, Chance PF (February 2000). X-Linked syndrome of polyendocrinopathy, immune dysfunction, and diarrhea maps to Xp11.23-Xq13.3. Am. J. Hum. Genet. 66 (2): 461—468. doi:10.1086/302761. PMC 1288099. PMID 10677306.
Tan B, Anaka M, Deb S, Freyer C, Ebert LM, Chueh AC, Al-Obaidi S, Behren A, Jayachandran A, Cebon J, Chen W, Mariadason JM (20 грудня 2013). FOXP3 over-expression inhibits melanoma tumorigenesis via effects on proliferation and apoptosis. Oncotarget. 5 (1): 264—76. PMC 3960207. PMID 24406338.

uniprot.org

UniProt, Q9BZS1 (англ.) . Архів оригіналу за 13 лютого 2018. Процитовано 12 лютого 2018.

web.archive.org

HUGO Gene Nomenclature Commitee, HGNC:6106 (англ.) . Архів оригіналу за 13 лютого 2018. Процитовано 12 лютого 2018. [Архівовано 2018-02-13 у Wayback Machine.]
UniProt, Q9BZS1 (англ.) . Архів оригіналу за 13 лютого 2018. Процитовано 12 лютого 2018.

wikidata.org

Захворювання, генетично пов'язані з FOXP3 переглянути/редагувати посилання на ВікіДаних.