152 related articles for article (PubMed ID: 32459745)
1. MYO5B Pathogenic Variants Found to Cause Intestinal Symptoms Without Microvillus Inclusion Disease in a Child Who Previously Underwent Liver Transplantation for PFIC-like Cholestasis.
Jarasvaraparn C; He M; Granadillo JL; Kulkarni S; Stoll J; Liss K
J Pediatr Gastroenterol Nutr; 2021 Jan; 72(1):e22-e24. PubMed ID: 32459745
[TBL] [Abstract][Full Text] [Related]
2. MYO5B mutations cause cholestasis with normal serum gamma-glutamyl transferase activity in children without microvillous inclusion disease.
Gonzales E; Taylor SA; Davit-Spraul A; Thébaut A; Thomassin N; Guettier C; Whitington PF; Jacquemin E
Hepatology; 2017 Jan; 65(1):164-173. PubMed ID: 27532546
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. Unequal Effects of Myosin 5B Mutations in Liver and Intestine Determine the Clinical Presentation of Low-Gamma-Glutamyltransferase Cholestasis.
van IJzendoorn SCD; Li Q; Qiu YL; Wang JS; Overeem AW
Hepatology; 2020 Oct; 72(4):1461-1468. PubMed ID: 32583448
[No Abstract] [Full Text] [Related]
6. 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]
7. 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]
8. A Functional Relationship Between UNC45A and MYO5B Connects Two Rare Diseases With Shared Enteropathy.
Li Q; Zhou Z; Sun Y; Sun C; Klappe K; van IJzendoorn SCD
Cell Mol Gastroenterol Hepatol; 2022; 14(2):295-310. PubMed ID: 35421597
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. 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. PubMed ID: 24138727
[TBL] [Abstract][Full Text] [Related]
12. MYO5B-associated diseases: Novel liver-related variants and genotype-phenotype correlation.
Wang L; Qiu YL; Xu HM; Zhu J; Li SJ; OuYang WX; Yang YF; Lu Y; Xie XB; Xing QH; Wang JS
Liver Int; 2022 Feb; 42(2):402-411. PubMed ID: 34811877
[TBL] [Abstract][Full Text] [Related]
13. [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]
14. 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]
15. 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]
16. [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]
17. 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]
18. Microvilli as markers of disordered apical-membrane trafficking and assembly: bowel and liver.
Thompson RJ; Knisely AS
Hepatology; 2014 Jul; 60(1):34-6. PubMed ID: 24668851
[No Abstract] [Full Text] [Related]
19. Apical Membrane Alterations in Non-intestinal Organs in Microvillus Inclusion Disease.
Schlegel C; Weis VG; Knowles BC; Lapierre LA; Martin MG; Dickman P; Goldenring JR; Shub MD
Dig Dis Sci; 2018 Feb; 63(2):356-365. PubMed ID: 29218485
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
