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Dominic P Norris

Showing results (21-30 of 31) with videos related to

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BMC Developmental Biology|August 14, 2010
The novel mouse mutant, chuzhoi, has disruption of Ptk7 protein and exhibits defects in neural tube, heart and lung development and abnormal planar cell polarity in the earAnju Paudyal, Christine Damrau, Victoria L Patterson, et al.
Plos Genetics|June 9, 2016
Genetic Analysis Reveals a Hierarchy of Interactions between Polycystin-Encoding Genes and Genes Controlling Cilia Function during Left-Right DeterminationDaniel T Grimes, Jennifer L Keynton, Maria T Buenavista, et al.
Cells|January 22, 2024
<i>PKD1L1</i> Is Involved in Congenital ChylothoraxJonathan B Whitchurch, Sophia Schneider, Alina C Hilger, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|February 25, 2009
Mouse mutagenesis identifies novel roles for left-right patterning genes in pulmonary, craniofacial, ocular, and limb developmentAlexander Ermakov, Jonathan L Stevens, Elaine Whitehill, et al.
Human Mutation|November 22, 2011
Static respiratory cilia associated with mutations in Dnahc11/DNAH11: a mouse model of PCDJane S Lucas, Elizabeth C Adam, Patricia M Goggin, et al.
Cell|October 29, 2021
De novo identification of mammalian ciliary motility proteins using cryo-EMMiao Gui, Hannah Farley, Priyanka Anujan, et al.
BMC Proceedings|February 27, 2019
Proceedings of the 3rd BEAT-PCD Conference and 4th PCD Training SchoolHannah Farley, Bruna Rubbo, Zuzanna Bukowy-Bieryllo, et al.
BMC Proceedings|June 25, 2020
Proceedings of the 4<sup>th</sup> BEAT-PCD Conference and 5<sup>th</sup> PCD Training SchoolLaura E Gardner, Katie L Horton, Amelia Shoemark, et al.
Development (Cambridge, England)|October 9, 2014
ATMIN is a transcriptional regulator of both lung morphogenesis and ciliogenesisParaskevi Goggolidou, Jonathan L Stevens, Francesco Agueci, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 8, 2022
Biallelic DAW1 variants cause a motile ciliopathy characterized by laterality defects and subtle ciliary beating abnormalitiesJoseph S Leslie, Rim Hjeij, Asaf Vivante, et al.
Pageof 4

Showing results (21-30 of 31) with videos related to

Sort By:
Pageof 4
BMC Developmental Biology|August 14, 2010
The novel mouse mutant, chuzhoi, has disruption of Ptk7 protein and exhibits defects in neural tube, heart and lung development and abnormal planar cell polarity in the earAnju Paudyal, Christine Damrau, Victoria L Patterson, et al.
Plos Genetics|June 9, 2016
Genetic Analysis Reveals a Hierarchy of Interactions between Polycystin-Encoding Genes and Genes Controlling Cilia Function during Left-Right DeterminationDaniel T Grimes, Jennifer L Keynton, Maria T Buenavista, et al.
Cells|January 22, 2024
<i>PKD1L1</i> Is Involved in Congenital ChylothoraxJonathan B Whitchurch, Sophia Schneider, Alina C Hilger, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|February 25, 2009
Mouse mutagenesis identifies novel roles for left-right patterning genes in pulmonary, craniofacial, ocular, and limb developmentAlexander Ermakov, Jonathan L Stevens, Elaine Whitehill, et al.
Human Mutation|November 22, 2011
Static respiratory cilia associated with mutations in Dnahc11/DNAH11: a mouse model of PCDJane S Lucas, Elizabeth C Adam, Patricia M Goggin, et al.
Cell|October 29, 2021
De novo identification of mammalian ciliary motility proteins using cryo-EMMiao Gui, Hannah Farley, Priyanka Anujan, et al.
BMC Proceedings|February 27, 2019
Proceedings of the 3rd BEAT-PCD Conference and 4th PCD Training SchoolHannah Farley, Bruna Rubbo, Zuzanna Bukowy-Bieryllo, et al.
BMC Proceedings|June 25, 2020
Proceedings of the 4<sup>th</sup> BEAT-PCD Conference and 5<sup>th</sup> PCD Training SchoolLaura E Gardner, Katie L Horton, Amelia Shoemark, et al.
Development (Cambridge, England)|October 9, 2014
ATMIN is a transcriptional regulator of both lung morphogenesis and ciliogenesisParaskevi Goggolidou, Jonathan L Stevens, Francesco Agueci, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 8, 2022
Biallelic DAW1 variants cause a motile ciliopathy characterized by laterality defects and subtle ciliary beating abnormalitiesJoseph S Leslie, Rim Hjeij, Asaf Vivante, et al.
Pageof 4