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J Wlodarczyk

Showing results (91-100 of 102) with videos related to

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Journal of Pediatric Surgery|July 15, 2019
Heritable spina bifida in sheep: A potential model for fetal repair of myelomeningoceleJohn W Steele, Sharon Bayliss, John Bayliss, et al.
Frontiers in Cell and Developmental Biology|March 22, 2021
Somatic and <i>de novo</i> Germline Variants of <i>MEDs</i> in Human Neural Tube DefectsTian Tian, Xuanye Cao, Yongyan Chen, et al.
Development (Cambridge, England)|April 29, 2024
Optical coherence tomography-guided Brillouin microscopy highlights regional tissue stiffness differences during anterior neural tube closure in the Mthfd1l murine mutantYogeshwari S Ambekar, Carlo Donato Caiaffa, Bogdan J Wlodarczyk, et al.
Stem Cell Research & Therapy|December 5, 2024
Amniotic fluid-derived stem cells: potential factories of natural and mimetic strategies for congenital malformationsCristiane S R Fonteles, Julia Enterria-Rosales, Ying Lin, et al.
Nature Cell Biology|September 22, 2009
The planar cell polarity effector Fuz is essential for targeted membrane trafficking, ciliogenesis and mouse embryonic developmentRyan S Gray, Philip B Abitua, Bogdan J Wlodarczyk, et al.
Journal of Medical Genetics|August 22, 2020
<i>CIC de novo</i> loss of function variants contribute to cerebral folate deficiency by downregulating <i>FOLR1</i> expressionXuanye Cao, Annika Wolf, Sung-Eun Kim, et al.
Indoor Air|December 22, 2018
Oxidative capacity and hemolytic activity of settled dust from moisture-damaged schoolsKati Huttunen, Anna J Wlodarczyk, Jenni Tirkkonen, et al.
Cell Discovery|February 27, 2023
Excess folic acid intake increases DNA de novo point mutationsXuanye Cao, Jianfeng Xu, Ying L Lin, et al.
Human Mutation|September 2, 2022
CIC missense variants contribute to susceptibility for spina bifidaXiao Han, Xuanye Cao, Vanessa Aguiar-Pulido, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 19, 2018
Formate rescues neural tube defects caused by mutations in <i>Slc25a32</i>Jimi Kim, Yunping Lei, Jin Guo, et al.
Pageof 11

Showing results (91-100 of 102) with videos related to

Sort By:
Pageof 11
Journal of Pediatric Surgery|July 15, 2019
Heritable spina bifida in sheep: A potential model for fetal repair of myelomeningoceleJohn W Steele, Sharon Bayliss, John Bayliss, et al.
Frontiers in Cell and Developmental Biology|March 22, 2021
Somatic and <i>de novo</i> Germline Variants of <i>MEDs</i> in Human Neural Tube DefectsTian Tian, Xuanye Cao, Yongyan Chen, et al.
Development (Cambridge, England)|April 29, 2024
Optical coherence tomography-guided Brillouin microscopy highlights regional tissue stiffness differences during anterior neural tube closure in the Mthfd1l murine mutantYogeshwari S Ambekar, Carlo Donato Caiaffa, Bogdan J Wlodarczyk, et al.
Stem Cell Research & Therapy|December 5, 2024
Amniotic fluid-derived stem cells: potential factories of natural and mimetic strategies for congenital malformationsCristiane S R Fonteles, Julia Enterria-Rosales, Ying Lin, et al.
Nature Cell Biology|September 22, 2009
The planar cell polarity effector Fuz is essential for targeted membrane trafficking, ciliogenesis and mouse embryonic developmentRyan S Gray, Philip B Abitua, Bogdan J Wlodarczyk, et al.
Journal of Medical Genetics|August 22, 2020
<i>CIC de novo</i> loss of function variants contribute to cerebral folate deficiency by downregulating <i>FOLR1</i> expressionXuanye Cao, Annika Wolf, Sung-Eun Kim, et al.
Indoor Air|December 22, 2018
Oxidative capacity and hemolytic activity of settled dust from moisture-damaged schoolsKati Huttunen, Anna J Wlodarczyk, Jenni Tirkkonen, et al.
Cell Discovery|February 27, 2023
Excess folic acid intake increases DNA de novo point mutationsXuanye Cao, Jianfeng Xu, Ying L Lin, et al.
Human Mutation|September 2, 2022
CIC missense variants contribute to susceptibility for spina bifidaXiao Han, Xuanye Cao, Vanessa Aguiar-Pulido, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 19, 2018
Formate rescues neural tube defects caused by mutations in <i>Slc25a32</i>Jimi Kim, Yunping Lei, Jin Guo, et al.
Pageof 11