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Nicholas J Cowan

Showing results (11-20 of 25) with videos related to

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Molecular Biology of the Cell|January 18, 2008
A pachygyria-causing alpha-tubulin mutation results in inefficient cycling with CCT and a deficient interaction with TBCBGuoling Tian, Xiang-Peng Kong, Xavier H Jaglin, et al.
Molecular Genetics & Genomic Medicine|November 30, 2016
A patient with lissencephaly, developmental delay, and infantile spasms, due to de novo heterozygous mutation of <i>KIF2A</i>Guoling Tian, Ana G Cristancho, Holly A Dubbs, et al.
The Journal of Biological Chemistry|August 13, 2003
Cytosolic Arl2 is complexed with cofactor D and protein phosphatase 2AJack F Shern, J Daniel Sharer, David C Pallas, et al.
The EMBO Journal|November 29, 2002
Structure of eukaryotic prefoldin and of its complexes with unfolded actin and the cytosolic chaperonin CCTJaime Martín-Benito, Jasminka Boskovic, Paulino Gómez-Puertas, et al.
Human Molecular Genetics|November 6, 2002
Localization in the human retina of the X-linked retinitis pigmentosa protein RP2, its homologue cofactor C and the RP2 interacting protein Arl3Celene Grayson, Francesca Bartolini, J Paul Chapple, et al.
Human Molecular Genetics|February 4, 2017
Infantile neurodegenerative disorder associated with mutations in TBCD, an essential gene in the tubulin heterodimer assembly pathwayShimon Edvardson, Guoling Tian, Hayley Cullen, et al.
Journal of Medical Genetics|June 9, 2016
Mutations in TUBB8 cause a multiplicity of phenotypes in human oocytes and early embryosRuizhi Feng, Zheng Yan, Bin Li, et al.
Molecular and Cellular Biology|July 7, 2011
Regulation of androgen receptor-mediated transcription by RPB5 binding protein URI/RMPPaolo Mita, Jeffrey N Savas, Nabil Djouder, et al.
Human Molecular Genetics|December 26, 2016
Uner Tan syndrome caused by a homozygous TUBB2B mutation affecting microtubule stabilityMartin W Breuss, Thai Nguyen, Anjana Srivatsan, et al.
Cell|January 16, 2007
Mutations in alpha-tubulin cause abnormal neuronal migration in mice and lissencephaly in humansDavid A Keays, Guoling Tian, Karine Poirier, et al.
Pageof 3

Showing results (11-20 of 25) with videos related to

Sort By:
Pageof 3
Molecular Biology of the Cell|January 18, 2008
A pachygyria-causing alpha-tubulin mutation results in inefficient cycling with CCT and a deficient interaction with TBCBGuoling Tian, Xiang-Peng Kong, Xavier H Jaglin, et al.
Molecular Genetics & Genomic Medicine|November 30, 2016
A patient with lissencephaly, developmental delay, and infantile spasms, due to de novo heterozygous mutation of <i>KIF2A</i>Guoling Tian, Ana G Cristancho, Holly A Dubbs, et al.
The Journal of Biological Chemistry|August 13, 2003
Cytosolic Arl2 is complexed with cofactor D and protein phosphatase 2AJack F Shern, J Daniel Sharer, David C Pallas, et al.
The EMBO Journal|November 29, 2002
Structure of eukaryotic prefoldin and of its complexes with unfolded actin and the cytosolic chaperonin CCTJaime Martín-Benito, Jasminka Boskovic, Paulino Gómez-Puertas, et al.
Human Molecular Genetics|November 6, 2002
Localization in the human retina of the X-linked retinitis pigmentosa protein RP2, its homologue cofactor C and the RP2 interacting protein Arl3Celene Grayson, Francesca Bartolini, J Paul Chapple, et al.
Human Molecular Genetics|February 4, 2017
Infantile neurodegenerative disorder associated with mutations in TBCD, an essential gene in the tubulin heterodimer assembly pathwayShimon Edvardson, Guoling Tian, Hayley Cullen, et al.
Journal of Medical Genetics|June 9, 2016
Mutations in TUBB8 cause a multiplicity of phenotypes in human oocytes and early embryosRuizhi Feng, Zheng Yan, Bin Li, et al.
Molecular and Cellular Biology|July 7, 2011
Regulation of androgen receptor-mediated transcription by RPB5 binding protein URI/RMPPaolo Mita, Jeffrey N Savas, Nabil Djouder, et al.
Human Molecular Genetics|December 26, 2016
Uner Tan syndrome caused by a homozygous TUBB2B mutation affecting microtubule stabilityMartin W Breuss, Thai Nguyen, Anjana Srivatsan, et al.
Cell|January 16, 2007
Mutations in alpha-tubulin cause abnormal neuronal migration in mice and lissencephaly in humansDavid A Keays, Guoling Tian, Karine Poirier, et al.
Pageof 3