Basal body (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Basal body" in English language version.

refsWebsite

Global rank English rank

19nih.gov

4^th place

13doi.org

2^nd place

6semanticscholar.org

11^th place

8^th place

1books.google.com

3^rd place

1harvard.edu

18^th place

17^th place

books.google.com

Benjamin Lewin (2007). Cells. Jones & Bartlett Learning. p. 359. ISBN 978-0-7637-3905-8. Retrieved 28 July 2019.

doi.org

Bloodgood, R. A. (2009). "From Central to Rudimentary to Primary: The History of an Underappreciated Organelle Whose Time Has Come.The Primary Cilium". Primary Cilia. Methods in Cell Biology. Vol. 94. pp. 3–52. doi:10.1016/S0091-679X(08)94001-2. ISBN 9780123750242. PMID 20362083.
Schrøder, Jacob M.; Larsen, Jesper; Komarova, Yulia; Akhmanova, Anna; Thorsteinsson, Rikke I.; Grigoriev, Ilya; Manguso, Robert; Christensen, Søren T.; Pedersen, Stine F.; Geimer, Stefan; Pedersen, Lotte B. (2011). "EB1 and EB3 promote cilia biogenesis by several centrosome-related mechanisms". Journal of Cell Science. 124 (15): 2539–2551. doi:10.1242/jcs.085852. PMC 3138699. PMID 21768326.
Kim, S.; Dynlacht, B. D. (2013). "Assembling a primary cilium". Current Opinion in Cell Biology. 25 (4): 506–511. doi:10.1016/j.ceb.2013.04.011. PMC 3729615. PMID 23747070.
Klos Dehring, D. A.; Vladar, E. K.; Werner, M. E.; Mitchell, J. W.; Hwang, P.; Mitchell, B. J. (2013). "Deuterosome-mediated centriole biogenesis". Developmental Cell. 27 (1): 103–112. doi:10.1016/j.devcel.2013.08.021. PMC 3816757. PMID 24075808.
Pearson, C. G.; Giddings Jr, T. H.; Winey, M. (2009). "Basal body components exhibit differential protein dynamics during nascent basal body assembly". Molecular Biology of the Cell. 20 (3): 904–914. doi:10.1091/mbc.e08-08-0835. PMC 2633379. PMID 19056680.
Ansley, S. J.; Badano, J. L.; Blacque, O. E.; Hill, J.; Hoskins, B. E.; Leitch, C. C.; Kim, J. C.; Ross, A. J.; Eichers, E. R.; Teslovich, T. M.; Mah, A. K.; Johnsen, R. C.; Cavender, J. C.; Lewis, R. A.; Leroux, M. R.; Beales, P. L.; Katsanis, N. (2003). "Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome". Nature. 425 (6958): 628–633. Bibcode:2003Natur.425..628A. doi:10.1038/nature02030. PMID 14520415. S2CID 4310157.
Ferrante, M. I.; Zullo, A.; Barra, A.; Bimonte, S.; Messaddeq, N.; Studer, M.; Dollé, P.; Franco, B. (2006). "Oral-facial-digital type I protein is required for primary cilia formation and left-right axis specification". Nature Genetics. 38 (1): 112–117. doi:10.1038/ng1684. PMID 16311594. S2CID 2441702.
Romio, L.; Fry, A. M.; Winyard, P. J.; Malcolm, S.; Woolf, A. S.; Feather, S. A. (2004). "OFD1 is a centrosomal/Basal body protein expressed during mesenchymal-epithelial transition in human nephrogenesis". Journal of the American Society of Nephrology. 15 (10): 2556–2568. doi:10.1097/01.ASN.0000140220.46477.5C. PMID 15466260. S2CID 22088755.
Arts, H. H.; Doherty, D.; Van Beersum, S. E.; Parisi, M. A.; Letteboer, S. J.; Gorden, N. T.; Peters, T. A.; Märker, T.; Voesenek, K.; Kartono, A.; Ozyurek, H.; Farin, F. M.; Kroes, H. Y.; Wolfrum, U.; Brunner, H. G.; Cremers, F. P.; Glass, I. A.; Knoers, N. V.; Roepman, R. (2007). "Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome". Nature Genetics. 39 (7): 882–888. doi:10.1038/ng2069. PMID 17558407. S2CID 12910768.
Shu, X.; Fry, A. M.; Tulloch, B.; Manson, F. D.; Crabb, J. W.; Khanna, H.; Faragher, A. J.; Lennon, A.; He, S.; Trojan, P.; Giessl, A.; Wolfrum, U.; Vervoort, R.; Swaroop, A.; Wright, A. F. (2005). "RPGR ORF15 isoform co-localizes with RPGRIP1 at centrioles and basal bodies and interacts with nucleophosmin". Human Molecular Genetics. 14 (9): 1183–1197. doi:10.1093/hmg/ddi129. PMID 15772089.
Kyttälä, M.; Tallila, J.; Salonen, R.; Kopra, O.; Kohlschmidt, N.; Paavola-Sakki, P.; Peltonen, L.; Kestilä, M. (2006). "MKS1, encoding a component of the flagellar apparatus basal body proteome, is mutated in Meckel syndrome". Nature Genetics. 38 (2): 155–157. doi:10.1038/ng1714. PMID 16415886. S2CID 10676530.
Winkelbauer, M. E.; Schafer, J. C.; Haycraft, C. J.; Swoboda, P.; Yoder, B. K. (2005). "The C. Elegans homologs of nephrocystin-1 and nephrocystin-4 are cilia transition zone proteins involved in chemosensory perception". Journal of Cell Science. 118 (Pt 23): 5575–5587. doi:10.1242/jcs.02665. PMID 16291722. S2CID 16717895.
Shang, Y.; Tsao, C. C.; Gorovsky, M. A. (2005). "Mutational analyses reveal a novel function of the nucleotide-binding domain of gamma-tubulin in the regulation of basal body biogenesis". The Journal of Cell Biology. 171 (6): 1035–1044. doi:10.1083/jcb.200508184. PMC 2171320. PMID 16344310.

harvard.edu

ui.adsabs.harvard.edu

Ansley, S. J.; Badano, J. L.; Blacque, O. E.; Hill, J.; Hoskins, B. E.; Leitch, C. C.; Kim, J. C.; Ross, A. J.; Eichers, E. R.; Teslovich, T. M.; Mah, A. K.; Johnsen, R. C.; Cavender, J. C.; Lewis, R. A.; Leroux, M. R.; Beales, P. L.; Katsanis, N. (2003). "Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome". Nature. 425 (6958): 628–633. Bibcode:2003Natur.425..628A. doi:10.1038/nature02030. PMID 14520415. S2CID 4310157.

nih.gov

pubmed.ncbi.nlm.nih.gov

Bloodgood, R. A. (2009). "From Central to Rudimentary to Primary: The History of an Underappreciated Organelle Whose Time Has Come.The Primary Cilium". Primary Cilia. Methods in Cell Biology. Vol. 94. pp. 3–52. doi:10.1016/S0091-679X(08)94001-2. ISBN 9780123750242. PMID 20362083.
Schrøder, Jacob M.; Larsen, Jesper; Komarova, Yulia; Akhmanova, Anna; Thorsteinsson, Rikke I.; Grigoriev, Ilya; Manguso, Robert; Christensen, Søren T.; Pedersen, Stine F.; Geimer, Stefan; Pedersen, Lotte B. (2011). "EB1 and EB3 promote cilia biogenesis by several centrosome-related mechanisms". Journal of Cell Science. 124 (15): 2539–2551. doi:10.1242/jcs.085852. PMC 3138699. PMID 21768326.
Kim, S.; Dynlacht, B. D. (2013). "Assembling a primary cilium". Current Opinion in Cell Biology. 25 (4): 506–511. doi:10.1016/j.ceb.2013.04.011. PMC 3729615. PMID 23747070.
Klos Dehring, D. A.; Vladar, E. K.; Werner, M. E.; Mitchell, J. W.; Hwang, P.; Mitchell, B. J. (2013). "Deuterosome-mediated centriole biogenesis". Developmental Cell. 27 (1): 103–112. doi:10.1016/j.devcel.2013.08.021. PMC 3816757. PMID 24075808.
Pearson, C. G.; Giddings Jr, T. H.; Winey, M. (2009). "Basal body components exhibit differential protein dynamics during nascent basal body assembly". Molecular Biology of the Cell. 20 (3): 904–914. doi:10.1091/mbc.e08-08-0835. PMC 2633379. PMID 19056680.
Ansley, S. J.; Badano, J. L.; Blacque, O. E.; Hill, J.; Hoskins, B. E.; Leitch, C. C.; Kim, J. C.; Ross, A. J.; Eichers, E. R.; Teslovich, T. M.; Mah, A. K.; Johnsen, R. C.; Cavender, J. C.; Lewis, R. A.; Leroux, M. R.; Beales, P. L.; Katsanis, N. (2003). "Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome". Nature. 425 (6958): 628–633. Bibcode:2003Natur.425..628A. doi:10.1038/nature02030. PMID 14520415. S2CID 4310157.
Ferrante, M. I.; Zullo, A.; Barra, A.; Bimonte, S.; Messaddeq, N.; Studer, M.; Dollé, P.; Franco, B. (2006). "Oral-facial-digital type I protein is required for primary cilia formation and left-right axis specification". Nature Genetics. 38 (1): 112–117. doi:10.1038/ng1684. PMID 16311594. S2CID 2441702.
Romio, L.; Fry, A. M.; Winyard, P. J.; Malcolm, S.; Woolf, A. S.; Feather, S. A. (2004). "OFD1 is a centrosomal/Basal body protein expressed during mesenchymal-epithelial transition in human nephrogenesis". Journal of the American Society of Nephrology. 15 (10): 2556–2568. doi:10.1097/01.ASN.0000140220.46477.5C. PMID 15466260. S2CID 22088755.
Arts, H. H.; Doherty, D.; Van Beersum, S. E.; Parisi, M. A.; Letteboer, S. J.; Gorden, N. T.; Peters, T. A.; Märker, T.; Voesenek, K.; Kartono, A.; Ozyurek, H.; Farin, F. M.; Kroes, H. Y.; Wolfrum, U.; Brunner, H. G.; Cremers, F. P.; Glass, I. A.; Knoers, N. V.; Roepman, R. (2007). "Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome". Nature Genetics. 39 (7): 882–888. doi:10.1038/ng2069. PMID 17558407. S2CID 12910768.
Kobayashi, A.; Higashide, T.; Hamasaki, D.; Kubota, S.; Sakuma, H.; An, W.; Fujimaki, T.; McLaren, M. J.; Weleber, R. G.; Inana, G. (2000). "HRG4 (UNC119) mutation found in cone-rod dystrophy causes retinal degeneration in a transgenic model". Investigative Ophthalmology & Visual Science. 41 (11): 3268–3277. PMID 11006213.
Shu, X.; Fry, A. M.; Tulloch, B.; Manson, F. D.; Crabb, J. W.; Khanna, H.; Faragher, A. J.; Lennon, A.; He, S.; Trojan, P.; Giessl, A.; Wolfrum, U.; Vervoort, R.; Swaroop, A.; Wright, A. F. (2005). "RPGR ORF15 isoform co-localizes with RPGRIP1 at centrioles and basal bodies and interacts with nucleophosmin". Human Molecular Genetics. 14 (9): 1183–1197. doi:10.1093/hmg/ddi129. PMID 15772089.
Kyttälä, M.; Tallila, J.; Salonen, R.; Kopra, O.; Kohlschmidt, N.; Paavola-Sakki, P.; Peltonen, L.; Kestilä, M. (2006). "MKS1, encoding a component of the flagellar apparatus basal body proteome, is mutated in Meckel syndrome". Nature Genetics. 38 (2): 155–157. doi:10.1038/ng1714. PMID 16415886. S2CID 10676530.
Winkelbauer, M. E.; Schafer, J. C.; Haycraft, C. J.; Swoboda, P.; Yoder, B. K. (2005). "The C. Elegans homologs of nephrocystin-1 and nephrocystin-4 are cilia transition zone proteins involved in chemosensory perception". Journal of Cell Science. 118 (Pt 23): 5575–5587. doi:10.1242/jcs.02665. PMID 16291722. S2CID 16717895.
Shang, Y.; Tsao, C. C.; Gorovsky, M. A. (2005). "Mutational analyses reveal a novel function of the nucleotide-binding domain of gamma-tubulin in the regulation of basal body biogenesis". The Journal of Cell Biology. 171 (6): 1035–1044. doi:10.1083/jcb.200508184. PMC 2171320. PMID 16344310.

ncbi.nlm.nih.gov

Schrøder, Jacob M.; Larsen, Jesper; Komarova, Yulia; Akhmanova, Anna; Thorsteinsson, Rikke I.; Grigoriev, Ilya; Manguso, Robert; Christensen, Søren T.; Pedersen, Stine F.; Geimer, Stefan; Pedersen, Lotte B. (2011). "EB1 and EB3 promote cilia biogenesis by several centrosome-related mechanisms". Journal of Cell Science. 124 (15): 2539–2551. doi:10.1242/jcs.085852. PMC 3138699. PMID 21768326.
Kim, S.; Dynlacht, B. D. (2013). "Assembling a primary cilium". Current Opinion in Cell Biology. 25 (4): 506–511. doi:10.1016/j.ceb.2013.04.011. PMC 3729615. PMID 23747070.
Klos Dehring, D. A.; Vladar, E. K.; Werner, M. E.; Mitchell, J. W.; Hwang, P.; Mitchell, B. J. (2013). "Deuterosome-mediated centriole biogenesis". Developmental Cell. 27 (1): 103–112. doi:10.1016/j.devcel.2013.08.021. PMC 3816757. PMID 24075808.
Pearson, C. G.; Giddings Jr, T. H.; Winey, M. (2009). "Basal body components exhibit differential protein dynamics during nascent basal body assembly". Molecular Biology of the Cell. 20 (3): 904–914. doi:10.1091/mbc.e08-08-0835. PMC 2633379. PMID 19056680.
Shang, Y.; Tsao, C. C.; Gorovsky, M. A. (2005). "Mutational analyses reveal a novel function of the nucleotide-binding domain of gamma-tubulin in the regulation of basal body biogenesis". The Journal of Cell Biology. 171 (6): 1035–1044. doi:10.1083/jcb.200508184. PMC 2171320. PMID 16344310.

semanticscholar.org

api.semanticscholar.org

Ansley, S. J.; Badano, J. L.; Blacque, O. E.; Hill, J.; Hoskins, B. E.; Leitch, C. C.; Kim, J. C.; Ross, A. J.; Eichers, E. R.; Teslovich, T. M.; Mah, A. K.; Johnsen, R. C.; Cavender, J. C.; Lewis, R. A.; Leroux, M. R.; Beales, P. L.; Katsanis, N. (2003). "Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome". Nature. 425 (6958): 628–633. Bibcode:2003Natur.425..628A. doi:10.1038/nature02030. PMID 14520415. S2CID 4310157.
Ferrante, M. I.; Zullo, A.; Barra, A.; Bimonte, S.; Messaddeq, N.; Studer, M.; Dollé, P.; Franco, B. (2006). "Oral-facial-digital type I protein is required for primary cilia formation and left-right axis specification". Nature Genetics. 38 (1): 112–117. doi:10.1038/ng1684. PMID 16311594. S2CID 2441702.
Romio, L.; Fry, A. M.; Winyard, P. J.; Malcolm, S.; Woolf, A. S.; Feather, S. A. (2004). "OFD1 is a centrosomal/Basal body protein expressed during mesenchymal-epithelial transition in human nephrogenesis". Journal of the American Society of Nephrology. 15 (10): 2556–2568. doi:10.1097/01.ASN.0000140220.46477.5C. PMID 15466260. S2CID 22088755.
Arts, H. H.; Doherty, D.; Van Beersum, S. E.; Parisi, M. A.; Letteboer, S. J.; Gorden, N. T.; Peters, T. A.; Märker, T.; Voesenek, K.; Kartono, A.; Ozyurek, H.; Farin, F. M.; Kroes, H. Y.; Wolfrum, U.; Brunner, H. G.; Cremers, F. P.; Glass, I. A.; Knoers, N. V.; Roepman, R. (2007). "Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome". Nature Genetics. 39 (7): 882–888. doi:10.1038/ng2069. PMID 17558407. S2CID 12910768.
Kyttälä, M.; Tallila, J.; Salonen, R.; Kopra, O.; Kohlschmidt, N.; Paavola-Sakki, P.; Peltonen, L.; Kestilä, M. (2006). "MKS1, encoding a component of the flagellar apparatus basal body proteome, is mutated in Meckel syndrome". Nature Genetics. 38 (2): 155–157. doi:10.1038/ng1714. PMID 16415886. S2CID 10676530.
Winkelbauer, M. E.; Schafer, J. C.; Haycraft, C. J.; Swoboda, P.; Yoder, B. K. (2005). "The C. Elegans homologs of nephrocystin-1 and nephrocystin-4 are cilia transition zone proteins involved in chemosensory perception". Journal of Cell Science. 118 (Pt 23): 5575–5587. doi:10.1242/jcs.02665. PMID 16291722. S2CID 16717895.