Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 20 of 43

1.

Malignant pheochromocytomas/paragangliomas harbor mutations in transport and cell adhesion genes.

Wilzén A, Rehammar A, Muth A, Nilsson O, Tešan Tomić T, Wängberg B, Kristiansson E, Abel F.

Int J Cancer. 2016 May 1;138(9):2201-11. doi: 10.1002/ijc.29957. Epub 2015 Dec 30.

PMID:
26650627
2.

Cargo-selective apical exocytosis in epithelial cells is conducted by Myo5B, Slp4a, Vamp7, and Syntaxin 3.

Vogel GF, Klee KM, Janecke AR, Müller T, Hess MW, Huber LA.

J Cell Biol. 2015 Nov 9;211(3):587-604. doi: 10.1083/jcb.201506112.

3.

The localisation of the apical Par/Cdc42 polarity module is specifically affected in microvillus inclusion disease.

Michaux G, Massey-Harroche D, Nicolle O, Rabant M, Brousse N, Goulet O, Le Bivic A, Ruemmele FM.

Biol Cell. 2016 Jan;108(1):19-28. doi: 10.1111/boc.201500034. Epub 2015 Dec 8.

PMID:
26526116
4.

Unravelling the mechanism of action of enzyme replacement therapy in Fabry disease.

Ko Y, Lee C, Moon MH, Hong GR, Cheon CK, Lee JS.

J Hum Genet. 2016 Feb;61(2):143-9. doi: 10.1038/jhg.2015.123. Epub 2015 Oct 22.

PMID:
26490183
5.

Critical role of Rab11a-mediated recycling endosomes in the assembly of type I parainfluenza viruses.

Stone R, Hayashi T, Bajimaya S, Hodges E, Takimoto T.

Virology. 2016 Jan;487:11-8. doi: 10.1016/j.virol.2015.10.008. Epub 2015 Oct 17.

6.

Myosin 5b loss of function leads to defects in polarized signaling: implication for microvillus inclusion disease pathogenesis and treatment.

Kravtsov D, Mashukova A, Forteza R, Rodriguez MM, Ameen NA, Salas PJ.

Am J Physiol Gastrointest Liver Physiol. 2014 Nov 15;307(10):G992-G1001. doi: 10.1152/ajpgi.00180.2014. Epub 2014 Sep 25.

7.

Microvillous atrophy: atypical presentations.

Perry A, Bensallah H, Martinez-Vinson C, Berrebi D, Arbeille B, Salomon J, Goulet O, Marinier E, Drunat S, Samson-Bouma ME, Gérard B, Hugot JP.

J Pediatr Gastroenterol Nutr. 2014 Dec;59(6):779-85. doi: 10.1097/MPG.0000000000000526.

PMID:
25111220
8.

Gene expression correlations in human cancer cell lines define molecular interaction networks for epithelial phenotype.

Kohn KW, Zeeberg BM, Reinhold WC, Pommier Y.

PLoS One. 2014 Jun 18;9(6):e99269. doi: 10.1371/journal.pone.0099269. eCollection 2014.

9.

Myosin Vb uncoupling from RAB8A and RAB11A elicits microvillus inclusion disease.

Knowles BC, Roland JT, Krishnan M, Tyska MJ, Lapierre LA, Dickman PS, Goldenring JR, Shub MD.

J Clin Invest. 2014 Jul;124(7):2947-62. doi: 10.1172/JCI71651. Epub 2014 Jun 2.

10.

Loss of syntaxin 3 causes variant microvillus inclusion disease.

Wiegerinck CL, Janecke AR, Schneeberger K, Vogel GF, van Haaften-Visser DY, Escher JC, Adam R, Thöni CE, Pfaller K, Jordan AJ, Weis CA, Nijman IJ, Monroe GR, van Hasselt PM, Cutz E, Klumperman J, Clevers H, Nieuwenhuis EE, Houwen RH, van Haaften G, Hess MW, Huber LA, Stapelbroek JM, Müller T, Middendorp S.

Gastroenterology. 2014 Jul;147(1):65-68.e10. doi: 10.1053/j.gastro.2014.04.002. Epub 2014 Apr 12.

PMID:
24726755
11.

Myosin Vb and Rab11a regulate phosphorylation of ezrin in enterocytes.

Dhekne HS, Hsiao NH, Roelofs P, Kumari M, Slim CL, Rings EH, van Ijzendoorn SC.

J Cell Sci. 2014 Mar 1;127(Pt 5):1007-17. doi: 10.1242/jcs.137273. Epub 2014 Jan 10.

12.

MYO5B and bile salt export pump contribute to cholestatic liver disorder in microvillous inclusion disease.

Girard M, Lacaille F, Verkarre V, Mategot R, Feldmann G, Grodet A, Sauvat F, Irtan S, Davit-Spraul A, Jacquemin E, Ruemmele F, Rainteau D, Goulet O, Colomb V, Chardot C, Henrion-Caude A, Debray D.

Hepatology. 2014 Jul;60(1):301-10. doi: 10.1002/hep.26974. Epub 2014 May 27.

PMID:
24375397
13.

Genetic risk variants for dyslexia on chromosome 18 in a German cohort.

Mueller B, Ahnert P, Burkhardt J, Brauer J, Czepezauer I, Quente E, Boltze J, Wilcke A, Kirsten H.

Genes Brain Behav. 2014 Mar;13(3):350-6. doi: 10.1111/gbb.12118. Epub 2014 Feb 3.

14.

Rab11-FIP2 interaction with MYO5B regulates movement of Rab11a-containing recycling vesicles.

Schafer JC, Baetz NW, Lapierre LA, McRae RE, Roland JT, Goldenring JR.

Traffic. 2014 Mar;15(3):292-308. doi: 10.1111/tra.12146. Epub 2014 Jan 22.

15.

Structural insights into the globular tails of the human type v myosins Myo5a, Myo5b, And Myo5c.

Velvarska H, Niessing D.

PLoS One. 2013 Dec 10;8(12):e82065. doi: 10.1371/journal.pone.0082065. eCollection 2013.

16.

Microvillus inclusion disease: loss of Myosin vb disrupts intracellular traffic and cell polarity.

Thoeni CE, Vogel GF, Tancevski I, Geley S, Lechner S, Pfaller K, Hess MW, Müller T, Janecke AR, Avitzur Y, Muise A, Cutz E, Huber LA.

Traffic. 2014 Jan;15(1):22-42. doi: 10.1111/tra.12131. Epub 2013 Nov 19.

17.

An overview and online registry of microvillus inclusion disease patients and their MYO5B mutations.

van der Velde KJ, Dhekne HS, Swertz MA, Sirigu S, Ropars V, Vinke PC, Rengaw T, van den Akker PC, Rings EH, Houdusse A, van Ijzendoorn SC.

Hum Mutat. 2013 Dec;34(12):1597-605. doi: 10.1002/humu.22440. Epub 2013 Oct 16. Review.

PMID:
24014347
18.

Myosin Vb controls biogenesis of post-Golgi Rab10 carriers during axon development.

Liu Y, Xu XH, Chen Q, Wang T, Deng CY, Song BL, Du JL, Luo ZG.

Nat Commun. 2013;4:2005. doi: 10.1038/ncomms3005.

PMID:
23770993
19.

Bowel "dissection" in microvillus inclusion disease.

Chiang MC, Hsu JF, Hsueh C, Chao HC, Wang TH, Chen CP, Lai MW.

Pediatr Neonatol. 2015 Apr;56(2):129-31. doi: 10.1016/j.pedneo.2013.03.004. Epub 2013 Apr 19.

20.

Myosin Vb gene is associated with schizophrenia in Chinese Han population.

Chen Y, Tian L, Zhang F, Liu C, Lu T, Ruan Y, Wang L, Yan H, Yan J, Liu Q, Zhang H, Ma W, Yang J, Li K, Lv L, Zhang D, Yue W.

Psychiatry Res. 2013 May 15;207(1-2):13-8. doi: 10.1016/j.psychres.2013.02.026. Epub 2013 Apr 3.

PMID:
23561489

Supplemental Content

Loading ...
Support Center