These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
207 related articles for article (PubMed ID: 28899465)
1. [Clinical features and MYO5B mutations of a family affected by microvillus inclusion disease]. Cheng Y; Liang H; Cai NL; Guo L; Huang YG; Song YZ Zhongguo Dang Dai Er Ke Za Zhi; 2017 Sep; 19(9):968-974. PubMed ID: 28899465 [TBL] [Abstract][Full Text] [Related]
2. 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. PubMed ID: 24375397 [TBL] [Abstract][Full Text] [Related]
3. Editing Myosin VB Gene to Create Porcine Model of Microvillus Inclusion Disease, With Microvillus-Lined Inclusions and Alterations in Sodium Transporters. Engevik AC; Coutts AW; Kaji I; Rodriguez P; Ongaratto F; Saqui-Salces M; Medida RL; Meyer AR; Kolobova E; Engevik MA; Williams JA; Shub MD; Carlson DF; Melkamu T; Goldenring JR Gastroenterology; 2020 Jun; 158(8):2236-2249.e9. PubMed ID: 32112796 [TBL] [Abstract][Full Text] [Related]
4. 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. PubMed ID: 24014347 [TBL] [Abstract][Full Text] [Related]
6. MYO5B mutations in patients with microvillus inclusion disease presenting with transient renal Fanconi syndrome. Golachowska MR; van Dael CM; Keuning H; Karrenbeld A; Hoekstra D; Gijsbers CF; Benninga MA; Rings EH; van Ijzendoorn SC J Pediatr Gastroenterol Nutr; 2012 Apr; 54(4):491-8. PubMed ID: 22441677 [TBL] [Abstract][Full Text] [Related]
7. Functional characterization of mutations in the myosin Vb gene associated with microvillus inclusion disease. Szperl AM; Golachowska MR; Bruinenberg M; Prekeris R; Thunnissen AM; Karrenbeld A; Dijkstra G; Hoekstra D; Mercer D; Ksiazyk J; Wijmenga C; Wapenaar MC; Rings EH; van IJzendoorn SC J Pediatr Gastroenterol Nutr; 2011 Mar; 52(3):307-13. PubMed ID: 21206382 [TBL] [Abstract][Full Text] [Related]
8. [Phenotypic and genetic analysis of a family affected with microvillus inclusion disease]. Mao M; Guo L; Zhang Z; Wang B; Huang S; Song Y; Chen F; Wen W Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Dec; 33(6):792-796. PubMed ID: 27984607 [TBL] [Abstract][Full Text] [Related]
9. Microvillus inclusion disease, a diagnosis to consider when abnormal stools and neurological impairments run together due to a rare syntaxin 3 gene mutation. Julia J; Shui V; Mittal N; Heim-Hall J; Blanco CL J Neonatal Perinatal Med; 2019; 12(3):313-319. PubMed ID: 30909251 [TBL] [Abstract][Full Text] [Related]
12. Loss-of-function of MYO5B is the main cause of microvillus inclusion disease: 15 novel mutations and a CaCo-2 RNAi cell model. Ruemmele FM; Müller T; Schiefermeier N; Ebner HL; Lechner S; Pfaller K; Thöni CE; Goulet O; Lacaille F; Schmitz J; Colomb V; Sauvat F; Revillon Y; Canioni D; Brousse N; de Saint-Basile G; Lefebvre J; Heinz-Erian P; Enninger A; Utermann G; Hess MW; Janecke AR; Huber LA Hum Mutat; 2010 May; 31(5):544-51. PubMed ID: 20186687 [TBL] [Abstract][Full Text] [Related]
13. 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; 307(10):G992-G1001. PubMed ID: 25258405 [TBL] [Abstract][Full Text] [Related]
14. Identification of intestinal ion transport defects in microvillus inclusion disease. Kravtsov DV; Ahsan MK; Kumari V; van Ijzendoorn SC; Reyes-Mugica M; Kumar A; Gujral T; Dudeja PK; Ameen NA Am J Physiol Gastrointest Liver Physiol; 2016 Jul; 311(1):G142-55. PubMed ID: 27229121 [TBL] [Abstract][Full Text] [Related]
15. [Analysis of a child with Microvillus inclusion disease due to variants of MYO5B gene and a literature review]. Xia J; Zhang X; Liu H; Kong X Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2024 Mar; 41(3):339-344. PubMed ID: 38448026 [TBL] [Abstract][Full Text] [Related]
16. 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. PubMed ID: 24892806 [TBL] [Abstract][Full Text] [Related]
17. Microvillus inclusion disease with novel MYO5B pathogenic variants. Kwon R; Huang J; Oshima K; Warren M; Voltaggio L; Wang Y; Montgomery EA; Hutchings D Histopathology; 2021 Jul; 79(1):119-121. PubMed ID: 33544913 [No Abstract] [Full Text] [Related]
18. Prenatal diagnosis of microvillus inclusion disease. Chen CP; Su YN; Chern SR; Wu PC; Wang W Taiwan J Obstet Gynecol; 2011 Sep; 50(3):399-400. PubMed ID: 22030065 [No Abstract] [Full Text] [Related]
19. Two cases of microvillus inclusion disease caused by MYO5B deficiency with prenatal abnormalities. Lu J; Qi Y; Ding H; Yin A Prenat Diagn; 2022 Jan; 42(1):136-140. PubMed ID: 34816459 [TBL] [Abstract][Full Text] [Related]
20. The zebrafish goosepimples/myosin Vb mutant exhibits cellular attributes of human microvillus inclusion disease. Sidhaye J; Pinto CS; Dharap S; Jacob T; Bhargava S; Sonawane M Mech Dev; 2016 Nov; 142():62-74. PubMed ID: 27497746 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]