Cutz E - Search Results

1

Abnormal Rab11-Rab8-vesicles cluster in enterocytes of patients with microvillus inclusion disease.

Vogel GF, Janecke AR, Krainer IM, Gutleben K, Witting B, Mitton SG, Mansour S, Ballauff A, Roland JT, Engevik AC, Cutz E, Müller T, Goldenring JR, Huber LA, Hess MW. Vogel GF, et al. Among authors: cutz e. Traffic. 2017 Jul;18(7):453-464. doi: 10.1111/tra.12486. Epub 2017 May 17. Traffic. 2017. PMID: 28407399 Free PMC article.

2

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. Thoeni CE, et al. Among authors: cutz e. Traffic. 2014 Jan;15(1):22-42. doi: 10.1111/tra.12131. Epub 2013 Nov 19. Traffic. 2014. PMID: 24138727 Free article.

3

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. Wiegerinck CL, et al. Among authors: cutz e. Gastroenterology. 2014 Jul;147(1):65-68.e10. doi: 10.1053/j.gastro.2014.04.002. Epub 2014 Apr 12. Gastroenterology. 2014. PMID: 24726755

4

Disrupted apical exocytosis of cargo vesicles causes enteropathy in FHL5 patients with Munc18-2 mutations.

Vogel GF, van Rijn JM, Krainer IM, Janecke AR, Posovszky C, Cohen M, Searle C, Jantchou P, Escher JC, Patey N, Cutz E, Müller T, Middendorp S, Hess MW, Huber LA. Vogel GF, et al. Among authors: cutz e. JCI Insight. 2017 Jul 20;2(14):e94564. doi: 10.1172/jci.insight.94564. eCollection 2017 Jul 20. JCI Insight. 2017. PMID: 28724787 Free PMC article.

5

Multilabel immunofluorescence and antigen reprobing on formalin-fixed paraffin-embedded sections: novel applications for precision pathology diagnosis.

Pan J, Thoeni C, Muise A, Yeger H, Cutz E. Pan J, et al. Among authors: cutz e. Mod Pathol. 2016 Jun;29(6):557-69. doi: 10.1038/modpathol.2016.52. Epub 2016 Mar 4. Mod Pathol. 2016. PMID: 26939874 Free article.

6

Microvillus inclusion disease: an inherited defect of brush-border assembly and differentiation.

Cutz E, Rhoads JM, Drumm B, Sherman PM, Durie PR, Forstner GG. Cutz E, et al. N Engl J Med. 1989 Mar 9;320(10):646-51. doi: 10.1056/NEJM198903093201006. N Engl J Med. 1989. PMID: 2537465 No abstract available.

7

A novel nonsense mutation in the EpCAM gene in a patient with congenital tufting enteropathy.

Thoeni C, Amir A, Guo C, Zhang S, Avitzur Y, Heng YM, Cutz E, Muise AM. Thoeni C, et al. Among authors: cutz e. J Pediatr Gastroenterol Nutr. 2014 Jan;58(1):18-21. doi: 10.1097/MPG.0000000000000106. J Pediatr Gastroenterol Nutr. 2014. PMID: 24048167

8

Microvillous inclusion disease: report of a case with atypical features.

Mierau GW, Wills EJ, Wyatt-Ashmead J, Hoffenberg EJ, Cutz E. Mierau GW, et al. Among authors: cutz e. Ultrastruct Pathol. 2001 May-Jun;25(3):275-9. Ultrastruct Pathol. 2001. PMID: 11465482 Corrected and republished. Review.

9

Microvillous inclusion disease: report of a case with atypical features.

Mierau GW, Wills EJ, Wyatt-Ashmead J, Hoffenberg EJ, Cutz E. Mierau GW, et al. Among authors: cutz e. Ultrastruct Pathol. 2001 Nov-Dec;25(6):517-21. doi: 10.1080/019131201753343548. Ultrastruct Pathol. 2001. PMID: 11783915

10

Assessment of the efficacy of in vivo CFTR protein replacement therapy in CF mice.

Ramjeesingh M, Huan LJ, Wilschanski M, Durie P, Li C, Gyomorey K, Wang Y, Kent G, Tanswell KA, Cutz E, Ackerley C, Bear CE. Ramjeesingh M, et al. Among authors: cutz e. Hum Gene Ther. 1998 Mar 1;9(4):521-8. doi: 10.1089/hum.1998.9.4-521. Hum Gene Ther. 1998. PMID: 9525313

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