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For: Antony D, Brunner HG, Schmidts M. Ciliary Dyneins and Dynein Related Ciliopathies. Cells 2021;10:1885. [PMID: 34440654 DOI: 10.3390/cells10081885] [Cited by in Crossref: 9] [Cited by in F6Publishing: 11] [Article Influence: 9.0] [Reference Citation Analysis]
Number Citing Articles
1 Petriman NA, Loureiro‐lópez M, Taschner M, Zacharia NK, Georgieva MM, Boegholm N, Wang J, Mourão A, Russell RB, Andersen JS, Lorentzen E. Biochemically validated structural model of the 15‐subunit intraflagellar transport complex IFT‐B. The EMBO Journal 2022. [DOI: 10.15252/embj.2022112440] [Reference Citation Analysis]
2 Petriman NA, Loureiro-lópez M, Taschner M, Zacharia NK, Georgieva MM, Boegholm N, Mourão A, Russell RB, Andersen JS, Lorentzen E. Biochemically validated structural model of the 15-subunit IFT-B complex.. [DOI: 10.1101/2022.08.20.504624] [Reference Citation Analysis]
3 Fitzsimons LA, Brewer VL, Tucker KL. Hedgehog Morphogens Act as Growth Factors Critical to Pre- and Postnatal Cardiac Development and Maturation: How Primary Cilia Mediate Their Signal Transduction. Cells 2022;11:1879. [PMID: 35741008 DOI: 10.3390/cells11121879] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
4 Antony D, Gulec Yilmaz E, Gezdirici A, Slagter L, Bakey Z, Bornaun H, Tanidir IC, Van Dinh T, Brunner HG, Walentek P, Arnold SJ, Backofen R, Schmidts M. Spectrum of Genetic Variants in a Cohort of 37 Laterality Defect Cases. Front Genet 2022;13:861236. [DOI: 10.3389/fgene.2022.861236] [Reference Citation Analysis]
5 Antony D, Güleç EY, Bakey Z, Schüle I, Kim G, Skatulla I, Brunner HG, Arnold SJ, Schmidts M. Base editing derived models of human WDR34 and WDR60 disease alleles replicate retrograde IFT and hedgehog signaling defects and suggest disturbed Golgi protein transport.. [DOI: 10.1101/2022.03.14.483768] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
6 Niziolek M, Bicka M, Osinka A, Samsel Z, Sekretarska J, Poprzeczko M, Bazan R, Fabczak H, Joachimiak E, Wloga D. PCD Genes-From Patients to Model Organisms and Back to Humans. Int J Mol Sci 2022;23:1749. [PMID: 35163666 DOI: 10.3390/ijms23031749] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
7 Pedersen LB, Jurisch-yaksi N, Schmid F, Christensen ST. Cilia and Flagella. Reference Module in Life Sciences 2022. [DOI: 10.1016/b978-0-12-821618-7.00209-1] [Reference Citation Analysis]
8 刘 璇. Research Progress on Pathogenesis and Gene Diagnosis of Primary Ciliary Dyskinesia and Cystic Fibrosis in Children. ACM 2022;12:2912-2917. [DOI: 10.12677/acm.2022.124419] [Reference Citation Analysis]
9 查 阳. Progress in the Study of DZIP1L Gene and Autosomal Recessive Polycystic Kidney Disease. ACM 2022;12:928-932. [DOI: 10.12677/acm.2022.122135] [Reference Citation Analysis]
10 Chandra B, Tung ML, Hsu Y, Scheetz T, Sheffield VC. Retinal ciliopathies through the lens of Bardet-Biedl Syndrome: Past, present and future. Prog Retin Eye Res 2021;:101035. [PMID: 34929400 DOI: 10.1016/j.preteyeres.2021.101035] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
11 Alsamri MT, Alabdouli A, Iram D, Alkalbani AM, Almarzooqi AS, Souid AK, Vijayan R. A Study on the Genetics of Primary Ciliary Dyskinesia. J Clin Med 2021;10:5102. [PMID: 34768622 DOI: 10.3390/jcm10215102] [Reference Citation Analysis]