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For: Kempeneers C, Chilvers MA. To beat, or not to beat, that is question! The spectrum of ciliopathies. Pediatr Pulmonol 2018;53:1122-9. [DOI: 10.1002/ppul.24078] [Cited by in Crossref: 17] [Cited by in F6Publishing: 17] [Article Influence: 4.3] [Reference Citation Analysis]
Number Citing Articles
1 Rosenfeld CS. Male reproductive tract cilia beat to a different drummer. Proc Natl Acad Sci U S A 2019;116:3361-3. [PMID: 30692268 DOI: 10.1073/pnas.1900112116] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
2 Grotjahn DA, Lander GC. Setting the dynein motor in motion: New insights from electron tomography. J Biol Chem 2019;294:13202-17. [PMID: 31285262 DOI: 10.1074/jbc.REV119.003095] [Cited by in Crossref: 8] [Cited by in F6Publishing: 5] [Article Influence: 2.7] [Reference Citation Analysis]
3 Brndiarova M, Kvassayova J, Vojtkova J, Igaz M, Buday T, Plevkova J. Changes of Motile Ciliary Phenotype in Patients with Primary Ciliopathies. Adv Exp Med Biol 2021. [PMID: 33687727 DOI: 10.1007/5584_2021_617] [Reference Citation Analysis]
4 von der Heyde EL, Hallmann A. Babo1, formerly Vop1 and Cop1/2, is no eyespot photoreceptor but a basal body protein illuminating cell division in Volvox carteri. Plant J 2020;102:276-98. [PMID: 31778231 DOI: 10.1111/tpj.14623] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.7] [Reference Citation Analysis]
5 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] [Article Influence: 1.0] [Reference Citation Analysis]
6 Yakar O, Tatar A. INTU-related oral-facial-digital syndrome XVII: Clinical spectrum of a rare disorder. Am J Med Genet A 2021. [PMID: 34623732 DOI: 10.1002/ajmg.a.62527] [Reference Citation Analysis]
7 Marquez J, Mann N, Arana K, Deniz E, Ji W, Konstantino M, Mis EK, Deshpande C, Jeffries L, McGlynn J, Hugo H, Widmeier E, Konrad M, Tasic V, Morotti R, Baptista J, Ellard S, Lakhani SA, Hildebrandt F, Khokha MK. DLG5 variants are associated with multiple congenital anomalies including ciliopathy phenotypes. J Med Genet 2021;58:453-64. [PMID: 32631816 DOI: 10.1136/jmedgenet-2019-106805] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
8 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: 1] [Article Influence: 1.0] [Reference Citation Analysis]
9 Tan K, Liu P, Pang L, Yang W, Hou F. A human ciliopathy with polycystic ovarian syndrome and multiple subcutaneous cysts: A rare case report. Medicine (Baltimore) 2018;97:e13531. [PMID: 30558011 DOI: 10.1097/MD.0000000000013531] [Reference Citation Analysis]
10 Yepiskoposyan H, Talikka M, Vavassori S, Martin F, Sewer A, Gubian S, Luettich K, Peitsch MC, Hoeng J. Construction of a Suite of Computable Biological Network Models Focused on Mucociliary Clearance in the Respiratory Tract. Front Genet 2019;10:87. [PMID: 30828347 DOI: 10.3389/fgene.2019.00087] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
11 Bonefas KM, Iwase S. Soma-to-germline transformation in chromatin-linked neurodevelopmental disorders? FEBS J 2021. [PMID: 34514717 DOI: 10.1111/febs.16196] [Reference Citation Analysis]
12 Shamseldin HE, Shaheen R, Ewida N, Bubshait DK, Alkuraya H, Almardawi E, Howaidi A, Sabr Y, Abdalla EM, Alfaifi AY, Alghamdi JM, Alsagheir A, Alfares A, Morsy H, Hussein MH, Al-Muhaizea MA, Shagrani M, Al Sabban E, Salih MA, Meriki N, Khan R, Almugbel M, Qari A, Tulba M, Mahnashi M, Alhazmi K, Alsalamah AK, Nowilaty SR, Alhashem A, Hashem M, Abdulwahab F, Ibrahim N, Alshidi T, AlObeid E, Alenazi MM, Alzaidan H, Rahbeeni Z, Al-Owain M, Sogaty S, Seidahmed MZ, Alkuraya FS. The morbid genome of ciliopathies: an update. Genet Med 2020;22:1051-60. [PMID: 32055034 DOI: 10.1038/s41436-020-0761-1] [Cited by in Crossref: 16] [Cited by in F6Publishing: 20] [Article Influence: 8.0] [Reference Citation Analysis]
13 Helgert ND, Sula MM. Caroli Syndrome in a 6-Year-Old Rottweiler Dog. J Comp Pathol 2019;167:1-5. [PMID: 30898291 DOI: 10.1016/j.jcpa.2018.11.004] [Cited by in Crossref: 1] [Article Influence: 0.3] [Reference Citation Analysis]
14 Gower WA, Birnkrant DJ, Black JB, Noah TL. Pediatric Pulmonology Year in Review 2018: Rare lung disease, neuromuscular disease, and diagnostic testing. Pediatr Pulmonol 2019;54:1655-62. [DOI: 10.1002/ppul.24461] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
15 Marusiakova L, Durdik P, Jesenak M, Bugova G, Kvassayova J, Oppova D, Banovcin P. Ciliary beat frequency in children with adenoid hypertrophy. Pediatric Pulmonology 2020;55:666-73. [DOI: 10.1002/ppul.24622] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
16 Getwan M, Hoppmann A, Schlosser P, Grand K, Song W, Diehl R, Schroda S, Heeg F, Deutsch K, Hildebrandt F, Lausch E, Köttgen A, Lienkamp SS. Ttc30a affects tubulin modifications in a model for ciliary chondrodysplasia with polycystic kidney disease. Proc Natl Acad Sci U S A 2021;118:e2106770118. [PMID: 34548398 DOI: 10.1073/pnas.2106770118] [Reference Citation Analysis]
17 Wiegering A, Rüther U, Gerhardt C. The ciliary protein Rpgrip1l in development and disease. Developmental Biology 2018;442:60-8. [DOI: 10.1016/j.ydbio.2018.07.024] [Cited by in Crossref: 15] [Cited by in F6Publishing: 12] [Article Influence: 3.8] [Reference Citation Analysis]
18 Mathieu H, Patten SA, Aragon-Martin JA, Ocaka L, Simpson M, Child A, Moldovan F. Genetic variant of TTLL11 gene and subsequent ciliary defects are associated with idiopathic scoliosis in a 5-generation UK family. Sci Rep 2021;11:11026. [PMID: 34040021 DOI: 10.1038/s41598-021-90155-0] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
19 Zhao L, Xie H, Kang Y, Lin Y, Liu G, Sakato-Antoku M, Patel-King RS, Wang B, Wan C, King SM, Zhao C, Huang K. Heme-binding protein CYB5D1 is a radial spoke component required for coordinated ciliary beating. Proc Natl Acad Sci U S A 2021;118:e2015689118. [PMID: 33875586 DOI: 10.1073/pnas.2015689118] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
20 Brndiarova M, Mraz M, Kolkova Z, Cisarik F, Banovcin P. Sensenbrenner Syndrome Presenting with Severe Anorexia, Failure to Thrive, Chronic Kidney Disease and Angel-Shaped Middle Phalanges in Two Siblings. Mol Syndromol 2021;12:263-7. [PMID: 34421506 DOI: 10.1159/000515645] [Reference Citation Analysis]