PIEZO2

Piezo type mechanosensitive ion channel component 2
المعرفات
الأسماء المستعارة	family with sequence similarity 38, member A pseudogene, piezo-type mechanosensitive ion channel component 2, protein PIEZO2, Protein FAM38B, PIEZO2 variant 16, family with sequence similarity 38, member B2, PIEZO2, piezo-type mechanosensitive ion channel component 1 pseudogene
معرفات خارجية
أورثولوج
	n/a
	n/a
	n/a
	n/a
	n/a
	n/a
	ويكي بيانات
اعرض/عدّل إنسان

PIEZO2‏ (Piezo type mechanosensitive ion channel component 2) هوَ بروتين يُشَفر بواسطة جين PIEZO2 في الإنسان.[1][2][3][4]

المراجع

"Entrez Gene: Piezo-type mechanosensitive ion channel component 2"، مؤرشف من الأصل في 19 أبريل 2016، اطلع عليه بتاريخ 06 أغسطس 2013.
Coste B, Mathur J, Schmidt M, Earley TJ, Ranade S, Petrus MJ, Dubin AE, Patapoutian A (أكتوبر 2010)، "Piezo1 and Piezo2 are essential components of distinct mechanically activated cation channels"، Science، 330 (6000): 55–60، doi:10.1126/science.1193270، PMC 3062430، PMID 20813920.
Coste B, Houge G, Murray MF, Stitziel N, Bandell M, Giovanni MA, Philippakis A, Hoischen A, Riemer G, Steen U, Steen VM, Mathur J, Cox J, Lebo M, Rehm H, Weiss ST, Wood JN, Maas RL, Sunyaev SR, Patapoutian A (مارس 2013)، "Gain-of-function mutations in the mechanically activated ion channel PIEZO2 cause a subtype of Distal Arthrogryposis"، Proceedings of the National Academy of Sciences of the United States of America، 110 (12): 4667–72، doi:10.1073/pnas.1221400110، PMC 3607045، PMID 23487782.
McMillin MJ, Beck AE, Chong JX, Shively KM, Buckingham KJ, Gildersleeve HI, Aracena MI, Aylsworth AS, Bitoun P, Carey JC, Clericuzio CL, Crow YJ, Curry CJ, Devriendt K, Everman DB, Fryer A, Gibson K, Giovannucci Uzielli ML, Graham JM, Hall JG, Hecht JT, Heidenreich RA, Hurst JA, Irani S, Krapels IP, Leroy JG, Mowat D, Plant GT, Robertson SP, Schorry EK, Scott RH, Seaver LH, Sherr E, Splitt M, Stewart H, Stumpel C, Temel SG, Weaver DD, Whiteford M, Williams MS, Tabor HK, Smith JD, Shendure J, Nickerson DA, Bamshad MJ (مايو 2014)، "Mutations in PIEZO2 cause Gordon syndrome, Marden-Walker syndrome, and distal arthrogryposis type 5"، American Journal of Human Genetics، 94 (5): 734–44، doi:10.1016/j.ajhg.2014.03.015، PMC 4067551، PMID 24726473.

قراءة متعمقة

"Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies"، The American Journal of Psychiatry، 170 (2): 207–17، فبراير 2013، doi:10.1176/appi.ajp.2012.12020237، PMID 23377640.
Ahn MJ, Won HH, Lee J, Lee ST, Sun JM, Park YH, Ahn JS, Kwon OJ, Kim H, Shim YM, Kim J, Kim K, Kim YH, Park JY, Kim JW, Park K (مارس 2012)، "The 18p11.22 locus is associated with never smoker non-small cell lung cancer susceptibility in Korean populations"، Human Genetics، 131 (3): 365–72، doi:10.1007/s00439-011-1080-z، PMID 21866343.
Del-Aguila JL, Beitelshees AL, Cooper-Dehoff RM, Chapman AB, Gums JG, Bailey K, Gong Y, Turner ST, Johnson JA, Boerwinkle E (فبراير 2014)، "Genome-wide association analyses suggest NELL1 influences adverse metabolic response to HCTZ in African Americans"، The Pharmacogenomics Journal، 14 (1): 35–40، doi:10.1038/tpj.2013.3، PMC 3812324، PMID 23400010.
Coste B, Houge G, Murray MF, Stitziel N, Bandell M, Giovanni MA, Philippakis A, Hoischen A, Riemer G, Steen U, Steen VM, Mathur J, Cox J, Lebo M, Rehm H, Weiss ST, Wood JN, Maas RL, Sunyaev SR, Patapoutian A (مارس 2013)، "Gain-of-function mutations in the mechanically activated ion channel PIEZO2 cause a subtype of Distal Arthrogryposis"، Proceedings of the National Academy of Sciences of the United States of America، 110 (12): 4667–72، doi:10.1073/pnas.1221400110، PMC 3607045، PMID 23487782.
Wang X, Shaffer JR, Zeng Z, Begum F, Vieira AR, Noel J, Anjomshoaa I, Cuenco KT, Lee MK, Beck J, Boerwinkle E, Cornelis MC, Hu FB, Crosslin DR, Laurie CC, Nelson SC, Doheny KF, Pugh EW, Polk DE, Weyant RJ, Crout R, McNeil DW, Weeks DE, Feingold E, Marazita ML (ديسمبر 2012)، "Genome-wide association scan of dental caries in the permanent dentition"، BMC Oral Health، 12: 57، doi:10.1186/1472-6831-12-57، PMC 3574042، PMID 23259602.
Xiao R, Xu XZ (نوفمبر 2010)، "Mechanosensitive channels: in touch with Piezo"، Current Biology، 20 (21): R936-8، doi:10.1016/j.cub.2010.09.053، PMC 3018681، PMID 21056836.
Coste B (يناير 2011)، "[Feeling the pressure? Identification of two proteins activated by mechanical forces]"، Medecine Sciences، 27 (1): 17–9، doi:10.1051/medsci/201127117، PMID 21299953.
Dubin AE, Schmidt M, Mathur J, Petrus MJ, Xiao B, Coste B, Patapoutian A (سبتمبر 2012)، "Inflammatory signals enhance piezo2-mediated mechanosensitive currents"، Cell Reports، 2 (3): 511–7، doi:10.1016/j.celrep.2012.07.014، PMC 3462303، PMID 22921401.
Luykx JJ, Bakker SC, Lentjes E, Neeleman M, Strengman E, Mentink L, DeYoung J, de Jong S, Sul JH, Eskin E, van Eijk K, van Setten J, Buizer-Voskamp JE, Cantor RM, Lu A, van Amerongen M, van Dongen EP, Keijzers P, Kappen T, Borgdorff P, Bruins P, Derks EM, Kahn RS, Ophoff RA (فبراير 2014)، "Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid"، Molecular Psychiatry، 19 (2): 228–34، doi:10.1038/mp.2012.183، PMID 23319000.

بوابة طب
بوابة علم الأحياء الخلوي والجزيئي
بوابة الكيمياء الحيوية

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[1] "Entrez Gene: Piezo-type mechanosensitive ion channel component 2"، مؤرشف من الأصل في 19 أبريل 2016، اطلع عليه بتاريخ 06 أغسطس 2013.

[2] Coste B, Mathur J, Schmidt M, Earley TJ, Ranade S, Petrus MJ, Dubin AE, Patapoutian A (أكتوبر 2010)، "Piezo1 and Piezo2 are essential components of distinct mechanically activated cation channels"، Science، 330 (6000): 55–60، doi:10.1126/science.1193270، PMC 3062430، PMID 20813920.

[3] Coste B, Houge G, Murray MF, Stitziel N, Bandell M, Giovanni MA, Philippakis A, Hoischen A, Riemer G, Steen U, Steen VM, Mathur J, Cox J, Lebo M, Rehm H, Weiss ST, Wood JN, Maas RL, Sunyaev SR, Patapoutian A (مارس 2013)، "Gain-of-function mutations in the mechanically activated ion channel PIEZO2 cause a subtype of Distal Arthrogryposis"، Proceedings of the National Academy of Sciences of the United States of America، 110 (12): 4667–72، doi:10.1073/pnas.1221400110، PMC 3607045، PMID 23487782.

[4] McMillin MJ, Beck AE, Chong JX, Shively KM, Buckingham KJ, Gildersleeve HI, Aracena MI, Aylsworth AS, Bitoun P, Carey JC, Clericuzio CL, Crow YJ, Curry CJ, Devriendt K, Everman DB, Fryer A, Gibson K, Giovannucci Uzielli ML, Graham JM, Hall JG, Hecht JT, Heidenreich RA, Hurst JA, Irani S, Krapels IP, Leroy JG, Mowat D, Plant GT, Robertson SP, Schorry EK, Scott RH, Seaver LH, Sherr E, Splitt M, Stewart H, Stumpel C, Temel SG, Weaver DD, Whiteford M, Williams MS, Tabor HK, Smith JD, Shendure J, Nickerson DA, Bamshad MJ (مايو 2014)، "Mutations in PIEZO2 cause Gordon syndrome, Marden-Walker syndrome, and distal arthrogryposis type 5"، American Journal of Human Genetics، 94 (5): 734–44، doi:10.1016/j.ajhg.2014.03.015، PMC 4067551، PMID 24726473.