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For: Dhekne HS, Pylypenko O, Overeem AW, Zibouche M, Ferreira RJ, van der Velde KJ, Rings EHHM, Posovszky C, van der Sluijs P, Swertz MA, Houdusse A, van IJzendoorn SCD. MYO5B, STX3, and STXBP2 mutations reveal a common disease mechanism that unifies a subset of congenital diarrheal disorders: A mutation update. Hum Mutat 2018;39:333-44. [PMID: 29266534 DOI: 10.1002/humu.23386] [Cited by in Crossref: 22] [Cited by in F6Publishing: 22] [Article Influence: 5.5] [Reference Citation Analysis]
Number Citing Articles
1 Baothman A, Almalki H, Abumelha K, Alshegifi A, Baashar A. Type 5 Familial Hemophagocytic Lymphohistiocytosis in a Seven-year-old Girl Post Second Bone Marrow Transplantation with Failure to Thrive: STXBP2 Novel Mutation. Cureus 2019;11:e6246. [PMID: 31807395 DOI: 10.7759/cureus.6246] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]
2 Wang L, Qiu YL, Xu HM, Zhu J, Li SJ, OuYang WX, Yang YF, Lu Y, Xie XB, Xing QH, Wang JS. MYO5B-associated diseases: Novel liver-related variants and genotype-phenotype correlation. Liver Int 2021. [PMID: 34811877 DOI: 10.1111/liv.15104] [Reference Citation Analysis]
3 Wu Z, Gong H, Zhang M, Tong X, Ai H, Xiao S, Perez-Enciso M, Yang B, Huang L. A worldwide map of swine short tandem repeats and their associations with evolutionary and environmental adaptations. Genet Sel Evol 2021;53:39. [PMID: 33892623 DOI: 10.1186/s12711-021-00631-4] [Reference Citation Analysis]
4 Coluccio LM. Myosins and Disease. Adv Exp Med Biol 2020;1239:245-316. [PMID: 32451863 DOI: 10.1007/978-3-030-38062-5_12] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
5 Li Q, Sun Y, van IJzendoorn SCD. A Link between Intrahepatic Cholestasis and Genetic Variations in Intracellular Trafficking Regulators. Biology (Basel) 2021;10:119. [PMID: 33557414 DOI: 10.3390/biology10020119] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
6 Dhekne HS, Pylypenko O, Overeem AW, Zibouche M, Ferreira RJ, van der Velde KJ, Rings EHHM, Posovszky C, van der Sluijs P, Swertz MA, Houdusse A, van IJzendoorn SCD. MYO5B, STX3, and STXBP2 mutations reveal a common disease mechanism that unifies a subset of congenital diarrheal disorders: A mutation update. Hum Mutat 2018;39:333-44. [PMID: 29266534 DOI: 10.1002/humu.23386] [Cited by in Crossref: 22] [Cited by in F6Publishing: 22] [Article Influence: 5.5] [Reference Citation Analysis]
7 van IJzendoorn SCD, Li Q, Qiu YL, Wang JS, Overeem AW. Unequal effects of MYO5B mutations in liver and intestine determine the clinical presentation of low-GGT cholestasis. Hepatology. 2020. [PMID: 32583448 DOI: 10.1002/hep.31430] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 5.0] [Reference Citation Analysis]
8 Kwon R, Huang J, Oshima K, Warren M, Voltaggio L, Wang Y, Montgomery EA, Hutchings D. Microvillus inclusion disease with novel MYO5B pathogenic variants. Histopathology 2021;79:119-21. [PMID: 33544913 DOI: 10.1111/his.14348] [Reference Citation Analysis]
9 Lu J, Qi Y, Ding H, Yin A. Two cases of microvillus inclusion disease caused by MYO5B deficiency with prenatal abnormalities. Prenat Diagn 2021. [PMID: 34816459 DOI: 10.1002/pd.6068] [Reference Citation Analysis]
10 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]
11 Leng C, Rings EHHM, de Wildt SN, van IJzendoorn SCD. Pharmacological and Parenteral Nutrition-Based Interventions in Microvillus Inclusion Disease. J Clin Med 2020;10:E22. [PMID: 33374831 DOI: 10.3390/jcm10010022] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
12 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: 0.5] [Reference Citation Analysis]
13 Leng C, Sun Y, van IJzendoorn SCD. Risk and Clinical Significance of Idiopathic Preterm Birth in Microvillus Inclusion Disease. J Clin Med 2021;10:3935. [PMID: 34501384 DOI: 10.3390/jcm10173935] [Reference Citation Analysis]
14 O'Sullivan MJ, Lindsay AJ. The Endosomal Recycling Pathway-At the Crossroads of the Cell. Int J Mol Sci 2020;21:E6074. [PMID: 32842549 DOI: 10.3390/ijms21176074] [Cited by in Crossref: 7] [Cited by in F6Publishing: 9] [Article Influence: 3.5] [Reference Citation Analysis]
15 Aldrian D, Vogel GF, Frey TK, Ayyıldız Civan H, Aksu AÜ, Avitzur Y, Ramos Boluda E, Çakır M, Demir AM, Deppisch C, Duba HC, Düker G, Gerner P, Hertecant J, Hornová J, Kathemann S, Koeglmeier J, Koutroumpa A, Lanzersdorfer R, Lev-Tzion R, Lima R, Mansour S, Meissl M, Melek J, Miqdady M, Montoya JH, Posovszky C, Rachman Y, Siahanidou T, Tabbers M, Uhlig HH, Ünal S, Wirth S, Ruemmele FM, Hess MW, Huber LA, Müller T, Sturm E, Janecke AR. Congenital Diarrhea and Cholestatic Liver Disease: Phenotypic Spectrum Associated with MYO5B Mutations. J Clin Med 2021;10:481. [PMID: 33525641 DOI: 10.3390/jcm10030481] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
16 Leng C, Overeem AW, Cartón-Garcia F, Li Q, Klappe K, Kuipers J, Cui Y, Zuhorn IS, Arango D, van IJzendoorn SCD. Loss of MYO5B expression deregulates late endosome size which hinders mitotic spindle orientation. PLoS Biol 2019;17:e3000531. [PMID: 31682603 DOI: 10.1371/journal.pbio.3000531] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 1.7] [Reference Citation Analysis]
17 Comegna M, Amato F, Liguori R, Berni Canani R, Spagnuolo MI, Morroni M, Guarino A, Castaldo G. Two cases of microvillous inclusion disease caused by novel mutations in MYO5B gene. Clin Case Rep 2018;6:2451-6. [PMID: 30564347 DOI: 10.1002/ccr3.1879] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 0.8] [Reference Citation Analysis]
18 Bandyopadhyay T, Deswal S, Maria A, Phulware RH, Das P, Ahuja A. Microvillous inclusion disease as a cause of severe congenital diarrhea in a newborn. J Matern Fetal Neonatal Med 2021;:1-3. [PMID: 33843415 DOI: 10.1080/14767058.2021.1910656] [Reference Citation Analysis]
19 Overeem AW, Li Q, Qiu YL, Cartón-García F, Leng C, Klappe K, Dronkers J, Hsiao NH, Wang JS, Arango D, van Ijzendoorn SCD. A Molecular Mechanism Underlying Genotype-Specific Intrahepatic Cholestasis Resulting From MYO5B Mutations. Hepatology 2020;72:213-29. [PMID: 31750554 DOI: 10.1002/hep.31002] [Cited by in Crossref: 11] [Cited by in F6Publishing: 14] [Article Influence: 5.5] [Reference Citation Analysis]
20 Grassini DR, da Silva J, Hall TE, Baillie GJ, Simons C, Parton RG, Hogan BM, Smith KA. Myosin Vb is required for correct trafficking of N-cadherin and cardiac chamber ballooning. Dev Dyn 2019;248:284-95. [PMID: 30801852 DOI: 10.1002/dvdy.19] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
21 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: 4] [Article Influence: 2.3] [Reference Citation Analysis]
22 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: 9] [Article Influence: 3.7] [Reference Citation Analysis]
23 Yan W, Xiao Y, Zhang Y, Tao Y, Cao Y, Liu K, Cai W, Wang Y. Monogenic mutations in four cases of neonatal-onset watery diarrhea and a mutation review in East Asia. Orphanet J Rare Dis 2021;16:383. [PMID: 34503561 DOI: 10.1186/s13023-021-01995-y] [Reference Citation Analysis]
24 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: 8] [Article Influence: 2.7] [Reference Citation Analysis]