Zobrazeno 1 - 5 of 5 pro vyhledávání: '"Terry Tansey"'
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Akademický článek
Disruption of Mks1 localization to the mother centriole causes cilia defects and developmental malformations in Meckel-Gruber syndrome
Autor: Cheng Cui, Bishwanath Chatterjee, Deanne Francis, Qing Yu, Jovenal T. SanAgustin, Richard Francis, Terry Tansey, Charisse Henry, Baolin Wang, Bethan Lemley, Gregory J. Pazour, Cecilia W. Lo
Publikováno v: Disease Models & Mechanisms, Vol 4, Iss 1, Pp 43-56 (2011)
SUMMARY Meckel-Gruber syndrome (MKS) is a recessive disorder resulting in multiple birth defects that are associated with mutations affecting ciliogenesis. We recovered a mouse mutant with a mutation in the Mks1 gene (Mks1del64-323) that caused a 260
Externí odkaz: https://doaj.org/article/bf8f8da5e4e4498ebca37febe1fe095f
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2
Akademický článek
Wdpcp, a PCP protein required for ciliogenesis, regulates directional cell migration and cell polarity by direct modulation of the actin cytoskeleton.
Autor: Cheng Cui, Bishwanath Chatterjee, Thomas P Lozito, Zhen Zhang, Richard J Francis, Hisato Yagi, Lisa M Swanhart, Subramaniam Sanker, Deanne Francis, Qing Yu, Jovenal T San Agustin, Chandrakala Puligilla, Tania Chatterjee, Terry Tansey, Xiaoqin Liu, Matthew W Kelley, Elias T Spiliotis, Adam V Kwiatkowski, Rocky Tuan, Gregory J Pazour, Neil A Hukriede, Cecilia W Lo
Publikováno v: PLoS Biology, Vol 11, Iss 11, p e1001720 (2013)
Planar cell polarity (PCP) regulates cell alignment required for collective cell movement during embryonic development. This requires PCP/PCP effector proteins, some of which also play essential roles in ciliogenesis, highlighting the long-standing q
Externí odkaz: https://doaj.org/article/74d38beca1bc443a9a89ee1c2c5aae74
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3
Disruption of Mks1 localization to the mother centriole causes cilia defects and developmental malformations in Meckel-Gruber syndrome
Autor: Cheng Cui, Richard Francis, Deanne Francis, Terry Tansey, Jovenal T. SanAgustin, Charisse Henry, Bishwanath Chatterjee, Gregory J. Pazour, Cecilia W. Lo, Baolin Wang, Qing Yu, Bethan Lemley
Publikováno v: Disease Models & Mechanisms
Disease Models & Mechanisms, Vol 4, Iss 1, Pp 43-56 (2011)
SUMMARY Meckel-Gruber syndrome (MKS) is a recessive disorder resulting in multiple birth defects that are associated with mutations affecting ciliogenesis. We recovered a mouse mutant with a mutation in the Mks1 gene (Mks1del64-323) that caused a 260
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19d34f06d7a4cf465d26bd97e2bcf996
http://europepmc.org/articles/PMC3008963
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4
Massively parallel sequencing identifies the gene Megf8 with ENU-induced mutation causing heterotaxy
Autor: Joel Martin, Richard Francis, Bishwanath Chatterjee, Cheng Cui, Teresa M. Gunn, Zhen Zhang, Yongli Bai, Qing Yu, Feng Chen, Jan Fang Cheng, Steven L. Sabol, Len A. Pennacchio, Deanne Alpert, Yuko Yoshinaga, Kenneth L. Kramer, Wendy Schackwitz, Maxim Koriabine, Pieter J. de Jong, Cecilia W. Lo, Terry Tansey
Publikováno v: Proceedings of the National Academy of Sciences. 106:3219-3224
Forward genetic screens with ENU ( N -ethyl- N -nitrosourea) mutagenesis can facilitate gene discovery, but mutation identification is often difficult. We present the first study in which an ENU- induced mutation was identified by massively parallel
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d79324f830f179574367e08dab56fade
https://doi.org/10.1073/pnas.0813400106
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