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Cited by in F6Publishing
For: Adamiok-Ostrowska A, Piekiełko-Witkowska A. Ciliary Genes in Renal Cystic Diseases. Cells 2020;9:E907. [PMID: 32276433 DOI: 10.3390/cells9040907] [Cited by in Crossref: 9] [Cited by in F6Publishing: 5] [Article Influence: 4.5] [Reference Citation Analysis]
Number Citing Articles
1 Chowdhury P, Perera D, Powell RT, Talley T, Tripathi DN, Park YS, Mancini MA, Davies P, Stephan C, Coarfa C, Dere R. Therapeutically actionable signaling node to rescue AURKA driven loss of primary cilia in VHL-deficient cells. Sci Rep 2021;11:10461. [PMID: 34002003 DOI: 10.1038/s41598-021-89933-7] [Reference Citation Analysis]
2 Florea L, Caba L, Gorduza EV. Bardet-Biedl Syndrome-Multiple Kaleidoscope Images: Insight into Mechanisms of Genotype-Phenotype Correlations. Genes (Basel) 2021;12:1353. [PMID: 34573333 DOI: 10.3390/genes12091353] [Reference Citation Analysis]
3 Morleo M, Franco B. OFD Type I syndrome: lessons learned from a rare ciliopathy. Biochem Soc Trans 2020;48:1929-39. [PMID: 32897366 DOI: 10.1042/BST20191029] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
4 Ungricht R, Guibbal L, Lasbennes MC, Orsini V, Beibel M, Waldt A, Cuttat R, Carbone W, Basler A, Roma G, Nigsch F, Tchorz JS, Hoepfner D, Hoppe PS. Genome-wide screening in human kidney organoids identifies developmental and disease-related aspects of nephrogenesis. Cell Stem Cell 2021:S1934-5909(21)00449-5. [PMID: 34847364 DOI: 10.1016/j.stem.2021.11.001] [Cited by in Crossref: 10] [Cited by in F6Publishing: 4] [Article Influence: 10.0] [Reference Citation Analysis]
5 König JC, Karsay R, Gerß J, Schlingmann K, Dahmer-heath M, Telgmann A, Kollmann S, Ariceta G, Gillion V, Bockenhauer D, Bertholet-thomas A, Mastrangelo A, Boyer O, Lilien M, Decramer S, Schanstra J, Pohl M, Schild R, Weber S, Hoefele J, Drube J, Cetiner M, Hansen M, Thumfart J, Tönshoff B, Habbig S, Liebau MC, Bald M, Bergmann C, Pennekamp P, Konrad M. Refining Kidney Survival in 383 Genetically Characterized Patients With Nephronophthisis. Kidney International Reports 2022. [DOI: 10.1016/j.ekir.2022.05.035] [Reference Citation Analysis]
6 Liu JL, Shen Q, Wu MY, Zhu GH, Li YF, Wang XW, Tang XS, Bi YL, Gong YN, Chen J, Fang XY, Zhai YH, Wu BB, Li GM, Sun YB, Gao XJ, Liu CH, Jiang XY, Hao S, Kang YL, Gong YL, Rong LP, Li D, Wang S, Ma D, Rao J, Xu H; for Chinese Children Genetic Kidney Disease Database (CCGKDD), “Internet Plus” Nephrology Alliance of the National Center for Children’s Care. Responsible genes in children with primary vesicoureteral reflux: findings from the Chinese Children Genetic Kidney Disease Database. World J Pediatr 2021;17:409-18. [PMID: 34059960 DOI: 10.1007/s12519-021-00428-x] [Reference Citation Analysis]
7 Falconieri A, Minervini G, Quaglia F, Sartori G, Tosatto SCE. Characterization of the pVHL Interactome in Human Testis Using High-Throughput Library Screening. Cancers 2022;14:1009. [DOI: 10.3390/cancers14041009] [Reference Citation Analysis]
8 Barroso-Gil M, Olinger E, Sayer JA. Molecular genetics of renal ciliopathies. Biochem Soc Trans 2021;49:1205-20. [PMID: 33960378 DOI: 10.1042/BST20200791] [Reference Citation Analysis]
9 Man Y, Shang X, Liu C, Zhang W, Huang Q, Ma S, Shiang R, Zhang F, Zhang L, Zhang Z. Whole-Exome Sequencing Identifies the VHL Mutation (c.262T > C, p.Try88Arg) in Non-Obstructive Azoospermia-Associated Cystic Renal Cell Carcinoma. Current Oncology 2022;29:2376-84. [DOI: 10.3390/curroncol29040192] [Reference Citation Analysis]
10 de Fallois J, Schönauer R, Münch J, Nagel M, Popp B, Halbritter J. Challenging Disease Ontology by Instances of Atypical PKHD1 and PKD1 Genetics. Front Genet 2021;12:682565. [PMID: 34249099 DOI: 10.3389/fgene.2021.682565] [Reference Citation Analysis]