KCNK5
KCNK5 (Potassium two pore domain channel subfamily K member 5) هوَ بروتين يُشَفر بواسطة جين KCNK5 في الإنسان.[1][2][3]
الوظيفة
المراجع
- "Entrez Gene: KCNK5 potassium channel, subfamily K, member 5". مؤرشف من الأصل في 2010-12-05.
- Goldstein SA، Bayliss DA، Kim D، Lesage F، Plant LD، Rajan S (ديسمبر 2005). "International Union of Pharmacology. LV. Nomenclature and molecular relationships of two-P potassium channels". Pharmacol Rev. ج. 57 ع. 4: 527–40. DOI:10.1124/pr.57.4.12. PMID:16382106.
- Reyes R، Duprat F، Lesage F، Fink M، Salinas M، Farman N، Lazdunski M (ديسمبر 1998). "Cloning and expression of a novel pH-sensitive two pore domain K+ channel from human kidney". J Biol Chem. ج. 273 ع. 47: 30863–9. DOI:10.1074/jbc.273.47.30863. PMID:9812978.
قراءة متعمقة
- Goldstein SA، Bockenhauer D، O'Kelly I، Zilberberg N (2001). "Potassium leak channels and the KCNK family of two-P-domain subunits". Nat. Rev. Neurosci. ج. 2 ع. 3: 175–84. DOI:10.1038/35058574. PMID:11256078.
- Bonaldo MF، Lennon G، Soares MB (1997). "Normalization and subtraction: two approaches to facilitate gene discovery". Genome Res. ج. 6 ع. 9: 791–806. DOI:10.1101/gr.6.9.791. PMID:8889548.
- Gray AT، Zhao BB، Kindler CH، وآخرون (2000). "Volatile anesthetics activate the human tandem pore domain baseline K+ channel KCNK5". Anesthesiology. ج. 92 ع. 6: 1722–30. DOI:10.1097/00000542-200006000-00032. PMID:10839924.
- Strausberg RL، Feingold EA، Grouse LH، وآخرون (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. ج. 99 ع. 26: 16899–903. DOI:10.1073/pnas.242603899. PMC:139241. PMID:12477932.
- Morton MJ، O'Connell AD، Sivaprasadarao A، Hunter M (2003). "Determinants of pH sensing in the two-pore domain K(+) channels TASK-1 and -2". Pflügers Arch. ج. 445 ع. 5: 577–83. DOI:10.1007/s00424-002-0901-2. PMID:12634929.
- Niemeyer MI، Cid LP، Valenzuela X، وآخرون (2004). "Extracellular conserved cysteine forms an intersubunit disulphide bridge in the KCNK5 (TASK-2) K+ channel without having an essential effect upon activity". Mol. Membr. Biol. ج. 20 ع. 2: 185–91. DOI:10.1080/0968768031000084181. PMID:12851074.
- Ota T، Suzuki Y، Nishikawa T، وآخرون (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. ج. 36 ع. 1: 40–5. DOI:10.1038/ng1285. PMID:14702039.
- Rusznák Z، Pocsai K، Kovács I، وآخرون (2004). "Differential distribution of TASK-1, TASK-2 and TASK-3 immunoreactivities in the rat and human cerebellum". Cell. Mol. Life Sci. ج. 61 ع. 12: 1532–42. DOI:10.1007/s00018-004-4082-3. PMID:15197476.
- Gerhard DS، Wagner L، Feingold EA، وآخرون (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. ج. 14 ع. 10B: 2121–7. DOI:10.1101/gr.2596504. PMC:528928. PMID:15489334.
بوابة طب
بوابة الكيمياء الحيوية
بوابة علم الأحياء الخلوي والجزيئي
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.