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23. 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]
25. 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]
26. Autophagocytosis of the apical membrane in microvillus inclusion disease. Reinshagen K; Naim HY; Zimmer KP Gut; 2002 Oct; 51(4):514-21. PubMed ID: 12235073 [TBL] [Abstract][Full Text] [Related]
27. A Case Study of Intractable Diarrhea Due to Neonatal Microvillous Inclusion Disease. Bulut O; Ahishali B; Gulluoglu M; Arslanoglu S Fetal Pediatr Pathol; 2017 Aug; 36(4):340-343. PubMed ID: 28707991 [TBL] [Abstract][Full Text] [Related]
28. CD10: a valuable tool for the light microscopic diagnosis of microvillous inclusion disease (familial microvillous atrophy). Groisman GM; Amar M; Livne E Am J Surg Pathol; 2002 Jul; 26(7):902-7. PubMed ID: 12131157 [TBL] [Abstract][Full Text] [Related]
29. Features of gastric and colonic mucosa in congenital enteropathies: a study in histology and immunohistochemistry. Treetipsatit J; Hazard FK Am J Surg Pathol; 2014 Dec; 38(12):1697-706. PubMed ID: 25007148 [TBL] [Abstract][Full Text] [Related]
30. Altered MYO5B Function Underlies Microvillus Inclusion Disease: Opportunities for Intervention at a Cellular Level. Bowman DM; Kaji I; Goldenring JR Cell Mol Gastroenterol Hepatol; 2022; 14(3):553-565. PubMed ID: 35660026 [TBL] [Abstract][Full Text] [Related]
31. Brush border myosin-I microinjected into cultured cells is targeted to actin-containing surface structures. Footer M; Bretscher A J Cell Sci; 1994 Jun; 107 ( Pt 6)():1623-31. PubMed ID: 7962202 [TBL] [Abstract][Full Text] [Related]
32. Congenital Fatal Diarrhea in Newborns. Lingaldinna S; Sundaram MB; Kamalarathnam CN; Bavanandam S Indian J Pediatr; 2017 Dec; 84(12):953-954. PubMed ID: 28842815 [TBL] [Abstract][Full Text] [Related]
33. 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]
35. 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]
36. Structural and compositional analysis of early stages in microvillus assembly in the enterocyte of the chick embryo. Heintzelman MB; Mooseker MS Differentiation; 1990 Jun; 43(3):175-82. PubMed ID: 2387484 [TBL] [Abstract][Full Text] [Related]
37. Distribution of actin and the actin-associated proteins myosin, tropomyosin, alpha-actinin, vinculin, and villin in rat and bovine exocrine glands. Drenckhahn D; Mannherz HG Eur J Cell Biol; 1983 May; 30(2):167-76. PubMed ID: 11596490 [TBL] [Abstract][Full Text] [Related]
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40. [Intestinal failure and transplantation in microvillous inclusion disease]. Fernández Caamaño B; Quiles Blanco MJ; Fernández Tomé L; Burgos Lizáldez E; Sarría Osés J; Molina Arias M; Prieto Bozano G An Pediatr (Barc); 2015 Sep; 83(3):160-5. PubMed ID: 25547668 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]