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Yunping Lei

Showing results (41-50 of 57) with videos related to

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Biorxiv : the Preprint Server for Biology|July 19, 2024
Epigenetic regulation by TET1 in gene-environmental interactions influencing susceptibility to congenital malformationsBernard K van der Veer, Lehua Chen, Spyridon Champeris Tsaniras, et al.
Human Mutation|September 2, 2022
CIC missense variants contribute to susceptibility for spina bifidaXiao Han, Xuanye Cao, Vanessa Aguiar-Pulido, 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 Molecular Genetics|June 26, 2023
A non-coding insertional mutation of Grhl2 causes gene over-expression and multiple structural anomalies including cleft palate, spina bifida and encephaloceleZoe Crane-Smith, Sandra C P De Castro, Evanthia Nikolopoulou, 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.
The Journal of Nutrition|January 29, 2019
Maternal Lactase Polymorphism (rs4988235) Is Associated with Neural Tube Defects in Offspring in the National Birth Defects Prevention StudyThanh T Hoang, Yunping Lei, Laura E Mitchell, et al.
Molecular Genetics & Genomic Medicine|April 11, 2019
Maternal genetic markers for risk of celiac disease and their potential association with neural tube defects in offspringThanh T Hoang, Yunping Lei, Laura E Mitchell, et al.
American Journal of Hypertension|July 26, 2020
Maternal Hypertension-Related Genotypes and Congenital Heart DefectsYunping Lei, Katherine L Ludorf, Xiao Yu, et al.
Human Molecular Genetics|September 24, 2020
FKBP8 variants are risk factors for spina bifidaTian Tian, Xuanye Cao, Sung-Eun Kim, et al.
Nature Communications|May 28, 2021
Actuation enhances patterning in human neural tube organoidsAbdel Rahman Abdel Fattah, Brian Daza, Gregorius Rustandi, et al.
Pageof 6

Showing results (41-50 of 57) with videos related to

Sort By:
Pageof 6
Biorxiv : the Preprint Server for Biology|July 19, 2024
Epigenetic regulation by TET1 in gene-environmental interactions influencing susceptibility to congenital malformationsBernard K van der Veer, Lehua Chen, Spyridon Champeris Tsaniras, et al.
Human Mutation|September 2, 2022
CIC missense variants contribute to susceptibility for spina bifidaXiao Han, Xuanye Cao, Vanessa Aguiar-Pulido, 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 Molecular Genetics|June 26, 2023
A non-coding insertional mutation of Grhl2 causes gene over-expression and multiple structural anomalies including cleft palate, spina bifida and encephaloceleZoe Crane-Smith, Sandra C P De Castro, Evanthia Nikolopoulou, 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.
The Journal of Nutrition|January 29, 2019
Maternal Lactase Polymorphism (rs4988235) Is Associated with Neural Tube Defects in Offspring in the National Birth Defects Prevention StudyThanh T Hoang, Yunping Lei, Laura E Mitchell, et al.
Molecular Genetics & Genomic Medicine|April 11, 2019
Maternal genetic markers for risk of celiac disease and their potential association with neural tube defects in offspringThanh T Hoang, Yunping Lei, Laura E Mitchell, et al.
American Journal of Hypertension|July 26, 2020
Maternal Hypertension-Related Genotypes and Congenital Heart DefectsYunping Lei, Katherine L Ludorf, Xiao Yu, et al.
Human Molecular Genetics|September 24, 2020
FKBP8 variants are risk factors for spina bifidaTian Tian, Xuanye Cao, Sung-Eun Kim, et al.
Nature Communications|May 28, 2021
Actuation enhances patterning in human neural tube organoidsAbdel Rahman Abdel Fattah, Brian Daza, Gregorius Rustandi, et al.
Pageof 6