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For: Eriksson M, Ansved T, Anvret M, Carey N. A mammalian radial spokehead-like gene, RSHL1, at the myotonic dystrophy-1 locus. Biochem Biophys Res Commun 2001;281:835-41. [PMID: 11237735 DOI: 10.1006/bbrc.2001.4465] [Cited by in Crossref: 13] [Cited by in F6Publishing: 12] [Article Influence: 0.6] [Reference Citation Analysis]
Number Citing Articles
1 Barbé L, Finkbeiner S. Genetic and Epigenetic Interplay Define Disease Onset and Severity in Repeat Diseases. Front Aging Neurosci 2022;14:750629. [DOI: 10.3389/fnagi.2022.750629] [Reference Citation Analysis]
2 Marshall WF, Nonaka S. Cilia: tuning in to the cell's antenna. Curr Biol 2006;16:R604-14. [PMID: 16890522 DOI: 10.1016/j.cub.2006.07.012] [Cited by in Crossref: 210] [Cited by in F6Publishing: 186] [Article Influence: 13.1] [Reference Citation Analysis]
3 Kott E, Legendre M, Copin B, Papon JF, Dastot-Le Moal F, Montantin G, Duquesnoy P, Piterboth W, Amram D, Bassinet L, Beucher J, Beydon N, Deneuville E, Houdouin V, Journel H, Just J, Nathan N, Tamalet A, Collot N, Jeanson L, Le Gouez M, Vallette B, Vojtek AM, Epaud R, Coste A, Clement A, Housset B, Louis B, Escudier E, Amselem S. Loss-of-function mutations in RSPH1 cause primary ciliary dyskinesia with central-complex and radial-spoke defects. Am J Hum Genet 2013;93:561-70. [PMID: 23993197 DOI: 10.1016/j.ajhg.2013.07.013] [Cited by in Crossref: 108] [Cited by in F6Publishing: 95] [Article Influence: 12.0] [Reference Citation Analysis]
4 Yang P, Diener DR, Yang C, Kohno T, Pazour GJ, Dienes JM, Agrin NS, King SM, Sale WS, Kamiya R, Rosenbaum JL, Witman GB. Radial spoke proteins of Chlamydomonas flagella. J Cell Sci 2006;119:1165-74. [PMID: 16507594 DOI: 10.1242/jcs.02811] [Cited by in Crossref: 165] [Cited by in F6Publishing: 147] [Article Influence: 10.3] [Reference Citation Analysis]
5 Abbasi F, Miyata H, Shimada K, Morohoshi A, Nozawa K, Matsumura T, Xu Z, Pratiwi P, Ikawa M. RSPH6A is required for sperm flagellum formation and male fertility in mice. J Cell Sci 2018;131:jcs221648. [PMID: 30185526 DOI: 10.1242/jcs.221648] [Cited by in Crossref: 35] [Cited by in F6Publishing: 27] [Article Influence: 8.8] [Reference Citation Analysis]
6 Noone PG, Leigh MW, Sannuti A, Minnix SL, Carson JL, Hazucha M, Zariwala MA, Knowles MR. Primary ciliary dyskinesia: diagnostic and phenotypic features. Am J Respir Crit Care Med 2004;169:459-67. [PMID: 14656747 DOI: 10.1164/rccm.200303-365OC] [Cited by in Crossref: 499] [Cited by in F6Publishing: 199] [Article Influence: 26.3] [Reference Citation Analysis]
7 Ergoli M, Venditti M, Picillo E, Minucci S, Politano L. Study of expression of genes potentially responsible for reduced fitness in patients with myotonic dystrophy type 1 and identification of new biomarkers of testicular function. Mol Reprod Dev 2020;87:45-52. [PMID: 31840338 DOI: 10.1002/mrd.23307] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 2.7] [Reference Citation Analysis]
8 Paudel B, Gervasi MG, Porambo J, Caraballo DA, Tourzani DA, Mager J, Platt MD, Salicioni AM, Visconti PE. Sperm capacitation is associated with phosphorylation of the testis-specific radial spoke protein Rsph6a†. Biol Reprod 2019;100:440-54. [PMID: 30239614 DOI: 10.1093/biolre/ioy202] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 3.0] [Reference Citation Analysis]
9 Ferkol T, Leigh M. Primary ciliary dyskinesia and newborn respiratory distress. Semin Perinatol 2006;30:335-40. [PMID: 17142159 DOI: 10.1053/j.semperi.2005.11.001] [Cited by in Crossref: 42] [Cited by in F6Publishing: 39] [Article Influence: 2.8] [Reference Citation Analysis]
10 Buckley L, Lacey M, Ehrlich M. Epigenetics of the myotonic dystrophy-associated DMPK gene neighborhood. Epigenomics 2016;8:13-31. [PMID: 26756355 DOI: 10.2217/epi.15.104] [Cited by in Crossref: 15] [Cited by in F6Publishing: 13] [Article Influence: 2.5] [Reference Citation Analysis]
11 Larkin K, Fardaei M. Myotonic dystrophy--a multigene disorder. Brain Res Bull 2001;56:389-95. [PMID: 11719277 DOI: 10.1016/s0361-9230(01)00656-6] [Cited by in Crossref: 29] [Cited by in F6Publishing: 7] [Article Influence: 1.5] [Reference Citation Analysis]
12 Wei M, Sivadas P, Owen HA, Mitchell DR, Yang P. Chlamydomonas mutants display reversible deficiencies in flagellar beating and axonemal assembly. Cytoskeleton (Hoboken) 2010;67:71-80. [PMID: 20169531 DOI: 10.1002/cm.20422] [Cited by in Crossref: 11] [Cited by in F6Publishing: 12] [Article Influence: 0.9] [Reference Citation Analysis]
13 Leigh MW, Pittman JE, Carson JL, Ferkol TW, Dell SD, Davis SD, Knowles MR, Zariwala MA. Clinical and genetic aspects of primary ciliary dyskinesia/Kartagener syndrome. Genet Med 2009;11:473-87. [PMID: 19606528 DOI: 10.1097/GIM.0b013e3181a53562] [Cited by in Crossref: 246] [Cited by in F6Publishing: 138] [Article Influence: 18.9] [Reference Citation Analysis]