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Cited by in F6Publishing
For: 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]
Number Citing Articles
1 Campbell JR, Li H, Wang Y, Kozhemyakin M, Hunt AJ Jr, Liu X, Janz R, Heidelberger R. Phosphorylation of the Retinal Ribbon Synapse Specific t-SNARE Protein Syntaxin3B Is Regulated by Light via a Ca2 +-Dependent Pathway. Front Cell Neurosci 2020;14:587072. [PMID: 33192329 DOI: 10.3389/fncel.2020.587072] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
2 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]
3 Li Y, Jiang L, Wang L, Wang C, Liu C, Guo A, Liu M, Zhang L, Ma C, Zhang X, Gao S, Liu JY. p.His16Arg of STXBP1 (MUNC18-1) Associated With Syntaxin 3B Causes Autosomal Dominant Congenital Nystagmus. Front Cell Dev Biol 2020;8:591781. [PMID: 33251218 DOI: 10.3389/fcell.2020.591781] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
4 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]
5 Pournami F, Mk AK, Panackal AV, Nandakumar A, Prabhakar J, Jain N. Microvillus Inclusion Disease: A Rare Mutation of STX3 in Exon 9 Causing Fatal Congenital Diarrheal Disease. J Pediatr Genet. [DOI: 10.1055/s-0040-1716401] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]