141 related articles for article (PubMed ID: 34816459)
41. Challenges of Microvillus Inclusion Disease in the NICU.
Badawy A; Elfadul M; Aziabi M; Ageel HI; Aqeel A
Neoreviews; 2020 Sep; 21(9):e600-e604. PubMed ID: 32873653
[TBL] [Abstract][Full Text] [Related]
42. 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
Traffic; 2017 Jul; 18(7):453-464. PubMed ID: 28407399
[TBL] [Abstract][Full Text] [Related]
43. Monogenic mutations in four cases of neonatal-onset watery diarrhea and a mutation review in East Asia.
Yan W; Xiao Y; Zhang Y; Tao Y; Cao Y; Liu K; Cai W; Wang Y
Orphanet J Rare Dis; 2021 Sep; 16(1):383. PubMed ID: 34503561
[TBL] [Abstract][Full Text] [Related]
44. Kinetic signatures of myosin-5B, the motor involved in microvillus inclusion disease.
Heissler SM; Chinthalapudi K; Sellers JR
J Biol Chem; 2017 Nov; 292(44):18372-18385. PubMed ID: 28882893
[TBL] [Abstract][Full Text] [Related]
45. Navajo microvillous inclusion disease is due to a mutation in MYO5B.
Erickson RP; Larson-Thomé K; Valenzuela RK; Whitaker SE; Shub MD
Am J Med Genet A; 2008 Dec; 146A(24):3117-9. PubMed ID: 19006234
[TBL] [Abstract][Full Text] [Related]
46. UNC45A deficiency causes microvillus inclusion disease-like phenotype by impairing myosin VB-dependent apical trafficking.
Duclaux-Loras R; Lebreton C; Berthelet J; Charbit-Henrion F; Nicolle O; Revenu des Courtils C; Waich S; Valovka T; Khiat A; Rabant M; Racine C; Guerrera IC; Baptista J; Mahe MM; Hess MW; Durel B; Lefort N; Banal C; Parisot M; Talbotec C; Lacaille F; Ecochard-Dugelay E; Demir AM; Vogel GF; Faivre L; Rodrigues A; Fowler D; Janecke AR; Müller T; Huber LA; Rodrigues-Lima F; Ruemmele FM; Uhlig HH; Del Bene F; Michaux G; Cerf-Bensussan N; Parlato M
J Clin Invest; 2022 May; 132(10):. PubMed ID: 35575086
[TBL] [Abstract][Full Text] [Related]
47. The challenge of personalized cell biology: The example of microvillus inclusion disease.
Goldenring JR
Traffic; 2020 Jan; 21(1):169-171. PubMed ID: 31596022
[TBL] [Abstract][Full Text] [Related]
48. Extraintestinal manifestations in an infant with microvillus inclusion disease: complications or features of the disease?
Siahanidou T; Koutsounaki E; Skiathitou AV; Stefanaki K; Marinos E; Panajiotou I; Chouliaras G
Eur J Pediatr; 2013 Sep; 172(9):1271-5. PubMed ID: 23354788
[TBL] [Abstract][Full Text] [Related]
49. Pathogenic STX3 variants affecting the retinal and intestinal transcripts cause an early-onset severe retinal dystrophy in microvillus inclusion disease subjects.
Janecke AR; Liu X; Adam R; Punuru S; Viestenz A; Strauß V; Laass M; Sanchez E; Adachi R; Schatz MP; Saboo US; Mittal N; Rohrschneider K; Escher J; Ganesh A; Al Zuhaibi S; Al Murshedi F; AlSaleem B; Alfadhel M; Al Sinani S; Alkuraya FS; Huber LA; Müller T; Heidelberger R; Janz R
Hum Genet; 2021 Aug; 140(8):1143-1156. PubMed ID: 33974130
[TBL] [Abstract][Full Text] [Related]
50. 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]
51. 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]
52. Rab11 is a useful tool for the diagnosis of microvillous inclusion disease.
Talmon G; Holzapfel M; DiMaio DJ; Muirhead D
Int J Surg Pathol; 2012 Jun; 20(3):252-6. PubMed ID: 22169970
[TBL] [Abstract][Full Text] [Related]
53. 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]
54. 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; 127(Pt 5):1007-17. PubMed ID: 24413175
[TBL] [Abstract][Full Text] [Related]
55. Microvillous Inclusion Disease as a Cause of Protracted Diarrhea.
Phulware RH; Gahlot GPS; Malik R; Gupta SD; Das P
Indian J Pediatr; 2019 Sep; 86(9):854-856. PubMed ID: 31049800
[TBL] [Abstract][Full Text] [Related]
56. 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; 211(3):587-604. PubMed ID: 26553929
[TBL] [Abstract][Full Text] [Related]
57. Identifying Mutations of the Tetratricopeptide Repeat Domain 37 (TTC37) Gene in Infants With Intractable Diarrhea and a Comparison of Asian and Non-Asian Phenotype and Genotype: A Global Case-report Study of a Well-Defined Syndrome With Immunodeficiency.
Lee WI; Huang JL; Chen CC; Lin JL; Wu RC; Jaing TH; Ou LS
Medicine (Baltimore); 2016 Mar; 95(9):e2918. PubMed ID: 26945392
[TBL] [Abstract][Full Text] [Related]
58. 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]
59. Microvillus inclusion disease with prenatal ultrasound findings and postpartum confirmed.
Şeker E; Koç A
Prenat Diagn; 2022 Jan; 42(1):151-152. PubMed ID: 35038185
[No Abstract] [Full Text] [Related]
60. Fetal Bowel Abnormalities Suspected by Ultrasonography in Microvillus Inclusion Disease: Prevalence and Clinical Significance.
Sun Y; Leng C; van Ijzendoorn SCD
J Clin Med; 2022 Jul; 11(15):. PubMed ID: 35893420
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
