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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 ear
Anju 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 Determination
Daniel T Grimes, Jennifer L Keynton, Maria T Buenavista, et al.
Cells
|
January 22, 2024
<i>PKD1L1</i> Is Involved in Congenital Chylothorax
Jonathan 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 development
Alexander 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 PCD
Jane S Lucas, Elizabeth C Adam, Patricia M Goggin, et al.
Cell
|
October 29, 2021
De novo identification of mammalian ciliary motility proteins using cryo-EM
Miao Gui, Hannah Farley, Priyanka Anujan, et al.
BMC Proceedings
|
February 27, 2019
Proceedings of the 3rd BEAT-PCD Conference and 4th PCD Training School
Hannah 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 School
Laura 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 ciliogenesis
Paraskevi 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 abnormalities
Joseph S Leslie, Rim Hjeij, Asaf Vivante, et al.
Page
of 4
Search research articles
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Showing results (21-30 of 31) with videos related to
Sort By:
Page
of 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 ear
Anju 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 Determination
Daniel T Grimes, Jennifer L Keynton, Maria T Buenavista, et al.
Cells
|
January 22, 2024
<i>PKD1L1</i> Is Involved in Congenital Chylothorax
Jonathan 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 development
Alexander 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 PCD
Jane S Lucas, Elizabeth C Adam, Patricia M Goggin, et al.
Cell
|
October 29, 2021
De novo identification of mammalian ciliary motility proteins using cryo-EM
Miao Gui, Hannah Farley, Priyanka Anujan, et al.
BMC Proceedings
|
February 27, 2019
Proceedings of the 3rd BEAT-PCD Conference and 4th PCD Training School
Hannah 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 School
Laura 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 ciliogenesis
Paraskevi 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 abnormalities
Joseph S Leslie, Rim Hjeij, Asaf Vivante, et al.
Page
of 4