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Cited by in F6Publishing
For: Vogel GF, Hess MW, Pfaller K, Huber LA, Janecke AR, Müller T. Towards understanding microvillus inclusion disease. Mol Cell Pediatr 2016;3:3. [PMID: 26830108 DOI: 10.1186/s40348-016-0031-0] [Cited by in Crossref: 22] [Cited by in F6Publishing: 17] [Article Influence: 4.4] [Reference Citation Analysis]
Number Citing Articles
1 Mosa MH, Nicolle O, Maschalidi S, Sepulveda FE, Bidaud-Meynard A, Menche C, Michels BE, Michaux G, de Saint Basile G, Farin HF. Dynamic Formation of Microvillus Inclusions During Enterocyte Differentiation in Munc18-2-Deficient Intestinal Organoids. Cell Mol Gastroenterol Hepatol 2018;6:477-493.e1. [PMID: 30364784 DOI: 10.1016/j.jcmgh.2018.08.001] [Cited by in Crossref: 19] [Cited by in F6Publishing: 12] [Article Influence: 6.3] [Reference Citation Analysis]
2 Jayawardena D, Alrefai WA, Dudeja PK, Gill RK. Recent advances in understanding and managing malabsorption: focus on microvillus inclusion disease. F1000Res. 2019;8 (F1000 Faculty Rev):2061. [PMID: 31824659 DOI: 10.12688/f1000research.20762.1] [Cited by in Crossref: 8] [Cited by in F6Publishing: 6] [Article Influence: 4.0] [Reference Citation Analysis]
3 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. Abnormal Rab11-Rab8-vesicles cluster in enterocytes of patients with microvillus inclusion disease. Traffic 2017;18:453-64. [PMID: 28407399 DOI: 10.1111/tra.12486] [Cited by in Crossref: 30] [Cited by in F6Publishing: 27] [Article Influence: 7.5] [Reference Citation Analysis]
4 Rouhanifard SH, Lopez Aguilar A, Meng L, Moremen KW, Wu P. Engineered Glycocalyx Regulates Stem Cell Proliferation in Murine Crypt Organoids. Cell Chem Biol 2018;25:439-446.e5. [PMID: 29429899 DOI: 10.1016/j.chembiol.2018.01.010] [Cited by in Crossref: 8] [Cited by in F6Publishing: 7] [Article Influence: 2.7] [Reference Citation Analysis]
5 Jarasvaraparn C, He M, Granadillo JL, Kulkarni S, Stoll J, Liss K. MYO5B Pathogenic Variants Found to Cause Intestinal Symptoms Without Microvillus Inclusion Disease In A Child Who Previously Underwent Liver Transplantation For PFIC-like Cholestasis. J Pediatr Gastroenterol Nutr. 2020. [PMID: 32459745 DOI: 10.1097/mpg.0000000000002792] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
6 Liu L, Wang K, Liu J, Wei Y, Liu W, Zhang P, Hu J, Li B. Starvation effect on the morphology of microvilli in HeLa cells. Biochemical and Biophysical Research Communications 2019;514:1238-43. [DOI: 10.1016/j.bbrc.2019.05.073] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
7 Bidaud-Meynard A, Nicolle O, Heck M, Le Cunff Y, Michaux G. A V0-ATPase-dependent apical trafficking pathway maintains the polarity of the intestinal absorptive membrane. Development 2019;146:dev174508. [PMID: 31110027 DOI: 10.1242/dev.174508] [Cited by in Crossref: 11] [Cited by in F6Publishing: 7] [Article Influence: 5.5] [Reference Citation Analysis]
8 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. Pathogenic STX3 variants affecting the retinal and intestinal transcripts cause an early-onset severe retinal dystrophy in microvillus inclusion disease subjects. Hum Genet 2021;140:1143-56. [PMID: 33974130 DOI: 10.1007/s00439-021-02284-1] [Reference Citation Analysis]
9 Badawy A, Elfadul M, Aziabi M, Ageel HI, Aqeel A. Challenges of Microvillus Inclusion Disease in the NICU. Neoreviews 2020;21:e600-4. [PMID: 32873653 DOI: 10.1542/neo.21-9-e600] [Cited by in Crossref: 2] [Article Influence: 2.0] [Reference Citation Analysis]
10 Román-Fernández A, Bryant DM. Complex Polarity: Building Multicellular Tissues Through Apical Membrane Traffic. Traffic 2016;17:1244-61. [PMID: 27281121 DOI: 10.1111/tra.12417] [Cited by in Crossref: 42] [Cited by in F6Publishing: 30] [Article Influence: 8.4] [Reference Citation Analysis]
11 Gupta MP, Yonekawa Y, Campbell JP, Rusu I, Zahid S, Patel SN, Chau F, Jonas KE, Oltra E, Orlin A, Chang J, Horowitz J, Abramson DH, Marr B, Capone A, Paul Chan RV. Early Diagnosis and Management of Aggressive Posterior Vitreoretinopathy Presenting in Premature Neonates. Ophthalmic Surg Lasers Imaging Retina 2019;50:201-7. [PMID: 30998240 DOI: 10.3928/23258160-20190401-01] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
12 Naim HY, Zimmer KP, Nichols B. Molecular biology of the gut. Mol Cell Pediatr 2016;3:32. [PMID: 27518572 DOI: 10.1186/s40348-016-0059-1] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.2] [Reference Citation Analysis]
13 Rao MC. Physiology of Electrolyte Transport in the Gut: Implications for Disease. Compr Physiol 2019;9:947-1023. [PMID: 31187895 DOI: 10.1002/cphy.c180011] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 3.5] [Reference Citation Analysis]
14 Tang BL. SNAREs and developmental disorders. J Cell Physiol 2021;236:2482-504. [PMID: 32959907 DOI: 10.1002/jcp.30067] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
15 Priyamvada S, Saksena S, Alrefai WA, Dudeja PK. Intestinal Anion Absorption. Physiology of the Gastrointestinal Tract. Elsevier; 2018. pp. 1317-62. [DOI: 10.1016/b978-0-12-809954-4.00057-8] [Cited by in Crossref: 2] [Article Influence: 0.7] [Reference Citation Analysis]
16 Sadiq M, Choudry O, Kashyap AK, Velazquez DM. Congenital diarrhea in a newborn infant: A case report. World J Clin Pediatr 2019;8:43-8. [PMID: 31559144 DOI: 10.5409/wjcp.v8.i3.43] [Cited by in CrossRef: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
17 Julia J, Shui V, Mittal N, Heim-hall J, Blanco CL. Microvillus inclusion disease, a diagnosis to consider when abnormal stools and neurological impairments run together due to a rare syntaxin 3 gene mutation. NPM 2019;12:313-9. [DOI: 10.3233/npm-1852] [Cited by in Crossref: 7] [Cited by in F6Publishing: 2] [Article Influence: 3.5] [Reference Citation Analysis]