基底小体 (Japanese Wikipedia)

Analysis of information sources in references of the Wikipedia article "基底小体" in Japanese language version.

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books.google.com

Benjamin Lewin (2007). Cells. Jones & Bartlett Learning. pp. 359. ISBN 978-0-7637-3905-8 2019年7月28日閲覧。

doi.org

Schrøder, Jacob M.; Larsen, Jesper; Komarova, Yulia; Akhmanova, Anna; Thorsteinsson, Rikke I.; Grigoriev, Ilya; Manguso, Robert; Christensen, Søren T. et al. (2011-08-01). “EB1 and EB3 promote cilia biogenesis by several centrosome-related mechanisms”. Journal of Cell Science 124 (Pt 15): 2539–2551. doi:10.1242/jcs.085852. ISSN 1477-9137. PMC 3138699. PMID 21768326.
Kim, Sehyun; Dynlacht, Brian David (2013-08). “Assembling a primary cilium”. Current Opinion in Cell Biology 25 (4): 506–511. doi:10.1016/j.ceb.2013.04.011. ISSN 1879-0410. PMC 3729615. PMID 23747070.
Klos Dehring, Deborah A.; Vladar, Eszter K.; Werner, Michael E.; Mitchell, Jennifer W.; Hwang, Peter; Mitchell, Brian J. (2013-10-14). “Deuterosome-mediated centriole biogenesis”. Developmental Cell 27 (1): 103–112. doi:10.1016/j.devcel.2013.08.021. ISSN 1878-1551. PMC 3816757. PMID 24075808.
Pearson, Chad G.; Giddings, Thomas H.; Winey, Mark (2009-02). “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. ISSN 1939-4586. PMC 2633379. PMID 19056680.
Ansley, Stephen J.; Badano, Jose L.; Blacque, Oliver E.; Hill, Josephine; Hoskins, Bethan E.; Leitch, Carmen C.; Kim, Jun Chul; Ross, Alison J. et al. (2003-10-09). “Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome”. Nature 425 (6958): 628–633. doi:10.1038/nature02030. ISSN 1476-4687. PMID 14520415.
Ferrante, Maria Immacolata; Zullo, Alessandro; Barra, Adriano; Bimonte, Sabrina; Messaddeq, Nadia; Studer, Michèle; Dollé, Pascal; Franco, Brunella (2006-01). “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. ISSN 1061-4036. PMID 16311594.
Romio, Leila; Fry, Andrew M.; Winyard, Paul J. D.; Malcolm, Sue; Woolf, Adrian S.; Feather, Sally A. (2004-10). “OFD1 is a centrosomal/basal body protein expressed during mesenchymal-epithelial transition in human nephrogenesis”. Journal of the American Society of Nephrology: JASN 15 (10): 2556–2568. doi:10.1097/01.ASN.0000140220.46477.5C. ISSN 1046-6673. PMID 15466260.
Arts, Heleen H.; Doherty, Dan; van Beersum, Sylvia E. C.; Parisi, Melissa A.; Letteboer, Stef J. F.; Gorden, Nicholas T.; Peters, Theo A.; Märker, Tina et al. (2007-07). “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. ISSN 1061-4036. PMID 17558407.
Shu, X.; Fry, A. M.; Tulloch, B.; Manson, F. D. C.; Crabb, J. W.; Khanna, H.; Faragher, A. J.; Lennon, A. et al. (2005-05-01). “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. ISSN 0964-6906. PMID 15772089.
Kyttälä, Mira; Tallila, Jonna; Salonen, Riitta; Kopra, Outi; Kohlschmidt, Nicolai; Paavola-Sakki, Paulina; Peltonen, Leena; Kestilä, Marjo (2006-02). “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. ISSN 1061-4036. PMID 16415886.
Winkelbauer, Marlene E.; Schafer, Jenny C.; Haycraft, Courtney J.; Swoboda, Peter; Yoder, Bradley K. (2005-12-01). “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. ISSN 0021-9533. PMID 16291722.
Shang, Yuhua; Tsao, Che-Chia; Gorovsky, Martin A. (2005-12-19). “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. ISSN 0021-9525. PMC 2171320. PMID 16344310.

nih.gov

pubmed.ncbi.nlm.nih.gov

Schrøder, Jacob M.; Larsen, Jesper; Komarova, Yulia; Akhmanova, Anna; Thorsteinsson, Rikke I.; Grigoriev, Ilya; Manguso, Robert; Christensen, Søren T. et al. (2011-08-01). “EB1 and EB3 promote cilia biogenesis by several centrosome-related mechanisms”. Journal of Cell Science 124 (Pt 15): 2539–2551. doi:10.1242/jcs.085852. ISSN 1477-9137. PMC 3138699. PMID 21768326.
Kim, Sehyun; Dynlacht, Brian David (2013-08). “Assembling a primary cilium”. Current Opinion in Cell Biology 25 (4): 506–511. doi:10.1016/j.ceb.2013.04.011. ISSN 1879-0410. PMC 3729615. PMID 23747070.
Klos Dehring, Deborah A.; Vladar, Eszter K.; Werner, Michael E.; Mitchell, Jennifer W.; Hwang, Peter; Mitchell, Brian J. (2013-10-14). “Deuterosome-mediated centriole biogenesis”. Developmental Cell 27 (1): 103–112. doi:10.1016/j.devcel.2013.08.021. ISSN 1878-1551. PMC 3816757. PMID 24075808.
Pearson, Chad G.; Giddings, Thomas H.; Winey, Mark (2009-02). “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. ISSN 1939-4586. PMC 2633379. PMID 19056680.
Ansley, Stephen J.; Badano, Jose L.; Blacque, Oliver E.; Hill, Josephine; Hoskins, Bethan E.; Leitch, Carmen C.; Kim, Jun Chul; Ross, Alison J. et al. (2003-10-09). “Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome”. Nature 425 (6958): 628–633. doi:10.1038/nature02030. ISSN 1476-4687. PMID 14520415.
Ferrante, Maria Immacolata; Zullo, Alessandro; Barra, Adriano; Bimonte, Sabrina; Messaddeq, Nadia; Studer, Michèle; Dollé, Pascal; Franco, Brunella (2006-01). “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. ISSN 1061-4036. PMID 16311594.
Romio, Leila; Fry, Andrew M.; Winyard, Paul J. D.; Malcolm, Sue; Woolf, Adrian S.; Feather, Sally A. (2004-10). “OFD1 is a centrosomal/basal body protein expressed during mesenchymal-epithelial transition in human nephrogenesis”. Journal of the American Society of Nephrology: JASN 15 (10): 2556–2568. doi:10.1097/01.ASN.0000140220.46477.5C. ISSN 1046-6673. PMID 15466260.
Arts, Heleen H.; Doherty, Dan; van Beersum, Sylvia E. C.; Parisi, Melissa A.; Letteboer, Stef J. F.; Gorden, Nicholas T.; Peters, Theo A.; Märker, Tina et al. (2007-07). “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. ISSN 1061-4036. PMID 17558407.
Kobayashi, A.; Higashide, T.; Hamasaki, D.; Kubota, S.; Sakuma, H.; An, W.; Fujimaki, T.; McLaren, M. J. et al. (2000-10). “HRG4 (UNC119) mutation found in cone-rod dystrophy causes retinal degeneration in a transgenic model”. Investigative Ophthalmology & Visual Science 41 (11): 3268–3277. ISSN 0146-0404. PMID 11006213.
Shu, X.; Fry, A. M.; Tulloch, B.; Manson, F. D. C.; Crabb, J. W.; Khanna, H.; Faragher, A. J.; Lennon, A. et al. (2005-05-01). “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. ISSN 0964-6906. PMID 15772089.
Kyttälä, Mira; Tallila, Jonna; Salonen, Riitta; Kopra, Outi; Kohlschmidt, Nicolai; Paavola-Sakki, Paulina; Peltonen, Leena; Kestilä, Marjo (2006-02). “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. ISSN 1061-4036. PMID 16415886.
Winkelbauer, Marlene E.; Schafer, Jenny C.; Haycraft, Courtney J.; Swoboda, Peter; Yoder, Bradley K. (2005-12-01). “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. ISSN 0021-9533. PMID 16291722.
Shang, Yuhua; Tsao, Che-Chia; Gorovsky, Martin A. (2005-12-19). “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. ISSN 0021-9525. 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. et al. (2011-08-01). “EB1 and EB3 promote cilia biogenesis by several centrosome-related mechanisms”. Journal of Cell Science 124 (Pt 15): 2539–2551. doi:10.1242/jcs.085852. ISSN 1477-9137. PMC 3138699. PMID 21768326.
Kim, Sehyun; Dynlacht, Brian David (2013-08). “Assembling a primary cilium”. Current Opinion in Cell Biology 25 (4): 506–511. doi:10.1016/j.ceb.2013.04.011. ISSN 1879-0410. PMC 3729615. PMID 23747070.
Klos Dehring, Deborah A.; Vladar, Eszter K.; Werner, Michael E.; Mitchell, Jennifer W.; Hwang, Peter; Mitchell, Brian J. (2013-10-14). “Deuterosome-mediated centriole biogenesis”. Developmental Cell 27 (1): 103–112. doi:10.1016/j.devcel.2013.08.021. ISSN 1878-1551. PMC 3816757. PMID 24075808.
Pearson, Chad G.; Giddings, Thomas H.; Winey, Mark (2009-02). “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. ISSN 1939-4586. PMC 2633379. PMID 19056680.
Shang, Yuhua; Tsao, Che-Chia; Gorovsky, Martin A. (2005-12-19). “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. ISSN 0021-9525. PMC 2171320. PMID 16344310.

worldcat.org

search.worldcat.org

Schrøder, Jacob M.; Larsen, Jesper; Komarova, Yulia; Akhmanova, Anna; Thorsteinsson, Rikke I.; Grigoriev, Ilya; Manguso, Robert; Christensen, Søren T. et al. (2011-08-01). “EB1 and EB3 promote cilia biogenesis by several centrosome-related mechanisms”. Journal of Cell Science 124 (Pt 15): 2539–2551. doi:10.1242/jcs.085852. ISSN 1477-9137. PMC 3138699. PMID 21768326.
Kim, Sehyun; Dynlacht, Brian David (2013-08). “Assembling a primary cilium”. Current Opinion in Cell Biology 25 (4): 506–511. doi:10.1016/j.ceb.2013.04.011. ISSN 1879-0410. PMC 3729615. PMID 23747070.
Klos Dehring, Deborah A.; Vladar, Eszter K.; Werner, Michael E.; Mitchell, Jennifer W.; Hwang, Peter; Mitchell, Brian J. (2013-10-14). “Deuterosome-mediated centriole biogenesis”. Developmental Cell 27 (1): 103–112. doi:10.1016/j.devcel.2013.08.021. ISSN 1878-1551. PMC 3816757. PMID 24075808.
Pearson, Chad G.; Giddings, Thomas H.; Winey, Mark (2009-02). “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. ISSN 1939-4586. PMC 2633379. PMID 19056680.
Ansley, Stephen J.; Badano, Jose L.; Blacque, Oliver E.; Hill, Josephine; Hoskins, Bethan E.; Leitch, Carmen C.; Kim, Jun Chul; Ross, Alison J. et al. (2003-10-09). “Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome”. Nature 425 (6958): 628–633. doi:10.1038/nature02030. ISSN 1476-4687. PMID 14520415.
Ferrante, Maria Immacolata; Zullo, Alessandro; Barra, Adriano; Bimonte, Sabrina; Messaddeq, Nadia; Studer, Michèle; Dollé, Pascal; Franco, Brunella (2006-01). “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. ISSN 1061-4036. PMID 16311594.
Romio, Leila; Fry, Andrew M.; Winyard, Paul J. D.; Malcolm, Sue; Woolf, Adrian S.; Feather, Sally A. (2004-10). “OFD1 is a centrosomal/basal body protein expressed during mesenchymal-epithelial transition in human nephrogenesis”. Journal of the American Society of Nephrology: JASN 15 (10): 2556–2568. doi:10.1097/01.ASN.0000140220.46477.5C. ISSN 1046-6673. PMID 15466260.
Arts, Heleen H.; Doherty, Dan; van Beersum, Sylvia E. C.; Parisi, Melissa A.; Letteboer, Stef J. F.; Gorden, Nicholas T.; Peters, Theo A.; Märker, Tina et al. (2007-07). “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. ISSN 1061-4036. PMID 17558407.
Kobayashi, A.; Higashide, T.; Hamasaki, D.; Kubota, S.; Sakuma, H.; An, W.; Fujimaki, T.; McLaren, M. J. et al. (2000-10). “HRG4 (UNC119) mutation found in cone-rod dystrophy causes retinal degeneration in a transgenic model”. Investigative Ophthalmology & Visual Science 41 (11): 3268–3277. ISSN 0146-0404. PMID 11006213.
Shu, X.; Fry, A. M.; Tulloch, B.; Manson, F. D. C.; Crabb, J. W.; Khanna, H.; Faragher, A. J.; Lennon, A. et al. (2005-05-01). “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. ISSN 0964-6906. PMID 15772089.
Kyttälä, Mira; Tallila, Jonna; Salonen, Riitta; Kopra, Outi; Kohlschmidt, Nicolai; Paavola-Sakki, Paulina; Peltonen, Leena; Kestilä, Marjo (2006-02). “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. ISSN 1061-4036. PMID 16415886.
Winkelbauer, Marlene E.; Schafer, Jenny C.; Haycraft, Courtney J.; Swoboda, Peter; Yoder, Bradley K. (2005-12-01). “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. ISSN 0021-9533. PMID 16291722.
Shang, Yuhua; Tsao, Che-Chia; Gorovsky, Martin A. (2005-12-19). “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. ISSN 0021-9525. PMC 2171320. PMID 16344310.

worldcat.org

Pack, Phillip E.,. Cliffsnotes AP biology. Cliffs Notes, Inc. (4th edition ed.). Boston. ISBN 978-1-118-12799-5. OCLC 811003769