Citations for
1CFTR, MYO1A
Myosin Ia is required for CFTR brush border membrane trafficking and ion transport in the mouse small intestine.
Kravtsov DV, Caputo C, Collaco A, Hoekstra N, Egan ME, Mooseker MS, Ameen NA.
Traffic 13(8):1072-82. doi: 10.1111/j.1600-0854.2012.01368.x. Epub 2012 May 8. 2012
2MYO1A
Myosin-1A targets to microvilli using multiple membrane binding motifs in the tail homology 1 (TH1) domain.
Mazerik JN, Tyska MJ.
J Biol Chem 287(16):13104-15. doi: 10.1074/jbc.M111.336313. Epub 2012 Feb 24. 2012
3MYO1A
Brush border myosin Ia has tumor suppressor activity in the intestine.
Mazzolini R, Dopeso H, Mateo-Lozano S, Chang W, Rodrigues P, Bazzocco S, Alazzouzi H, Landolfi S, Hernández-Losa J, Andretta E, Alhopuro P, Espín E, Armengol M, Tabernero J, Ramón y Cajal S, Kloor M, Gebert J, Mariadason JM, Schwartz S Jr, Aaltonen LA, Mooseker MS, Arango D.
Proc Natl Acad Sci U S A 109(5):1530-5. doi: 10.1073/pnas.1108411109. Epub 2012 Jan 18. 2012
4MYO1A
Molecular model of the microvillar cytoskeleton and organization of the brush border.
Brown JW, McKnight CJ.
PLoS One 5(2):e9406. doi: 10.1371/journal.pone.0009406. 2010
5MYO1A
Differential localization and dynamics of class I myosins in the enterocyte microvillus.
Benesh AE, Nambiar R, McConnell RE, Mao S, Tabb DL, Tyska MJ.
Mol Biol Cell 21(6):970-8. doi: 10.1091/mbc.E09-07-0638. Epub 2010 Jan 20. 2010
6MYO1A
The enterocyte microvillus is a vesicle-generating organelle.
McConnell RE, Higginbotham JN, Shifrin DA Jr, Tabb DL, Coffey RJ, Tyska MJ.
J Cell Biol 185(7):1285-98. doi: 10.1083/jcb.200902147. 2009
7DFNA48, MYO1A
Human deafness mutation E385D disrupts the mechanochemical coupling and subcellular targeting of myosin-1a.
Yengo CM, Ananthanarayanan SK, Brosey CA, Mao S, Tyska MJ.
Biophys J 94(2):L5-7. Epub 2007 Nov 2. 2008
8MYO1A
Myosin-1a powers the sliding of apical membrane along microvillar actin bundles.
McConnell RE, Tyska MJ.
J Cell Biol 177(4):671-81. Epub 2007 May 14. 2007
9MYO1A, MYO1C
Myosin-1a is critical for normal brush border structure and composition.
Tyska MJ, Mackey AT, Huang JD, Copeland NG, Jenkins NA, Mooseker MS.
Mol Biol Cell 16(5):2443-57. Epub 2005 Mar 9. 2005
10DFNA48, MYO1A
Multiple mutations of MYO1A, a cochlear-expressed gene, in sensorineural hearing loss.
Donaudy F, Ferrara A, Esposito L, Hertzano R, Ben-David O, Bell RE, Melchionda S, Zelante L, Avraham KB, Gasparini P.
Am J Hum Genet 72(6):1571-7. Epub 2003 May 06. 2003
11MYO10, MYO1A, MYO1C, MYO1D, MYO7A, MYO5B, MYO7B, MYO1E, MYO1B, MYO1F
Mapping of unconventional myosins in mouse and human.
Hasson T, Skowron JF, Gilbert DJ, Avraham KB, Perry WL, Bement WM,Anderson BL, Sherr EH, Chen ZY, Greene LA, Ward DC, Corey DP, Mooseker MS,Copeland NG, Jenkins NA.
Genomics 36(3):431-9. 1996