Emerging and novel technologies in reproductive and developmental toxicology
Maier, Susan E., Cabrera, Robert M., Chen, Yichang, Vargesson, Neil
Published in Reproductive toxicology (Elmsford, N.Y.) (01.12.2024)
Published in Reproductive toxicology (Elmsford, N.Y.) (01.12.2024)
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Journal Article
Gene Environment Interactions in the Etiology of Neural Tube Defects
Finnell, Richard H, Caiaffa, Carlo Donato, Kim, Sung-Eun, Lei, Yunping, Steele, John, Cao, Xuanye, Tukeman, Gabriel, Lin, Ying Linda, Cabrera, Robert M, Wlodarczyk, Bogdan J
Published in Frontiers in genetics (10.05.2021)
Published in Frontiers in genetics (10.05.2021)
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Journal Article
Dolutegravir-induced neural tube defects in mice are folate responsive
Tukeman, Gabriel L, Wei, Hui, Lin, Ying L, Wlodarczyk, Bogdan J, Finnell, Richard H, Cabrera, Robert M
Published in AIDS (London) (15.03.2024)
Published in AIDS (London) (15.03.2024)
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Journal Article
The antagonism of folate receptor by dolutegravir: developmental toxicity reduction by supplemental folic acid
Cabrera, Robert M, Souder, Jaclyn P, Steele, John W, Yeo, Lythou, Tukeman, Gabriel, Gorelick, Daniel A, Finnell, Richard H
Published in AIDS (London) (01.11.2019)
Published in AIDS (London) (01.11.2019)
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Journal Article
Folate regulation of planar cell polarity pathway and F-actin through folate receptor alpha
Han, Xiao, Cao, Xuanye, Cabrera, Robert M, Ramirez, Paula Andrea Pimienta, Lin, Ying Linda, Wlodarczyk, Bogdan J, Zhang, Cuilian, Finnell, Richard H, Lei, Yunping
Published in The FASEB journal (01.01.2024)
Published in The FASEB journal (01.01.2024)
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Journal Article
Hypermethylation of PI3K-AKT signalling pathway genes is associated with human neural tube defects
Tian, Tian, Lai, Xinyuan, Xiang, Kuanhui, Han, Xiao, Yin, Shengju, Cabrera, Robert M., Steele, John W., Lei, Yunping, Cao, Xuanye, Finnell, Richard H., Wang, Linlin, Ren, Aiguo
Published in Epigenetics (01.02.2022)
Published in Epigenetics (01.02.2022)
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Journal Article
Formate rescues neural tube defects caused by mutations in Slc25a32
Kim, Jimi, Lei, Yunping, Guo, Jin, Kim, Sung-Eun, Wlodarczyk, Bogdan J., Cabrera, Robert M., Lin, Ying Linda, Nilsson, Torbjorn K., Zhang, Ting, Ren, Aiguo, Wang, Linlin, Yuan, Zhengwei, Zheng, Yu-Fang, Wang, Hong-Yan, Finnell, Richard H.
Published in Proceedings of the National Academy of Sciences - PNAS (01.05.2018)
Published in Proceedings of the National Academy of Sciences - PNAS (01.05.2018)
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Journal Article
LRP2 mediates folate uptake in the developing neural tube
Kur, Esther, Mecklenburg, Nora, Cabrera, Robert M, Willnow, Thomas E, Hammes, Annette
Published in Journal of cell science (15.05.2014)
Published in Journal of cell science (15.05.2014)
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Journal Article
CIC de novo loss of function variants contribute to cerebral folate deficiency by downregulating FOLR1 expression
Cao, Xuanye, Wolf, Annika, Kim, Sung-Eun, Cabrera, Robert M., Wlodarczyk, Bogdan J., Zhu, Huiping, Parker, Margaret, Lin, Ying, Steele, John W., Han, Xiao, Ramaekers, Vincent Th, Steinfeld, Robert, Finnell, Richard H., Lei, Yunping
Published in Journal of medical genetics (01.07.2021)
Published in Journal of medical genetics (01.07.2021)
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Journal Article
Impact of selective serotonin reuptake inhibitors on neural crest stem cell formation
Vichier-Guerre, Cecilia, Parker, Margaret, Pomerantz, Yael, Finnell, Richard H., Cabrera, Robert M.
Published in Toxicology letters (05.11.2017)
Published in Toxicology letters (05.11.2017)
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Journal Article
Approaches to studying the genomic architecture of complex birth defects
Taiwo, Toluwani E., Cao, Xuanye, Cabrera, Robert M., Lei, Yunping, Finnell, Richard H.
Published in Prenatal diagnosis (01.08.2020)
Published in Prenatal diagnosis (01.08.2020)
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Journal Article
CIC missense variants contribute to susceptibility for spina bifida
Han, Xiao, Cao, Xuanye, Aguiar‐Pulido, Vanessa, Yang, Wei, Karki, Menuka, Ramirez, Paula Andrea Pimienta, Cabrera, Robert M., Lin, Ying Linda, Wlodarczyk, Bogdan J., Shaw, Gary M., Ross, M. Elizabeth, Zhang, Cuilian, Finnell, Richard H., Lei, Yunping
Published in Human mutation (01.12.2022)
Published in Human mutation (01.12.2022)
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Journal Article
P147: Precision medicine approaches to treatment for HNRNPH2 mutations
Zhu, Huiping, Bowling, Rodney, Cabrera, Robert, Banks, Courtney, Finnell, Richard
Published in Genetics in Medicine Open (2024)
Published in Genetics in Medicine Open (2024)
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Journal Article
Dolutegravir induces FOLR1 expression during brain organoid development
Caiaffa, Carlo Donato, Tukeman, Gabriel, Delgado, Christian Zevallos, Ambekar, Yogeshwari S, Mekonnen, Taye T, Singh, Manmohan, Rodriguez, Victoria, Ricco, Emily, Kraushaar, Daniel, Aglyamov, Salavat R, Scarcelli, Giuliano, Larin, Kirill V, Finnell, Richard H, Cabrera, Robert M
Published in Frontiers in molecular neuroscience (17.05.2024)
Published in Frontiers in molecular neuroscience (17.05.2024)
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Journal Article
Characterization of folic acid, 5-methyltetrahydrofolate and synthetic folinic acid in the high-affinity folate transporters: impact on pregnancy and development
Palacios, Ana M, Feiner, Rachel A, Cabrera, Robert M
Published in Reproductive and Developmental Medicine (01.06.2023)
Published in Reproductive and Developmental Medicine (01.06.2023)
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Journal Article
FKBP8 variants are risk factors for spina bifida
Tian, Tian, Cao, Xuanye, Kim, Sung-Eun, Lin, Ying Linda, Steele, John W, Cabrera, Robert M, Karki, Menuka, Yang, Wei, Marini, Nicholas J, Hoffman, Ethan N, Han, Xiao, Hu, Cindy, Wang, Linlin, Wlodarczyk, Bogdan J, Shaw, Gary M, Ren, Aiguo, Finnell, Richard H, Lei, Yunping
Published in Human molecular genetics (04.11.2020)
Published in Human molecular genetics (04.11.2020)
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Journal Article
KDM6B Variants May Contribute to the Pathophysiology of Human Cerebral Folate Deficiency
Han, Xiao, Cao, Xuanye, Cabrera, Robert M, Pimienta Ramirez, Paula Andrea, Zhang, Cuilian, Ramaekers, Vincent T, Finnell, Richard H, Lei, Yunping
Published in Biology (Basel, Switzerland) (31.12.2022)
Published in Biology (Basel, Switzerland) (31.12.2022)
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Journal Article
Loss of RAD9B impairs early neural development and contributes to the risk for human spina bifida
Cao, Xuanye, Tian, Tian, Steele, John W., Cabrera, Robert M., Aguiar‐Pulido, Vanessa, Wadhwa, Shruti, Bhavani, Nikitha, Bi, Patrick, Gargurevich, Nick H., Hoffman, Ethan N., Cai, Chun‐Quan, Marini, Nicholas J., Yang, Wei, Shaw, Gary M., Ross, Margaret E., Finnell, Richard H., Lei, Yunping
Published in Human mutation (01.04.2020)
Published in Human mutation (01.04.2020)
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Journal Article
Heritable spina bifida in sheep: A potential model for fetal repair of myelomeningocele
Steele, John W., Bayliss, Sharon, Bayliss, John, Lin, Ying Linda, Wlodarczyk, Bogdan J., Cabrera, Robert M., Asfaw, Yohannes G., Cummings, Thomas J., Finnell, Richard H., George, Timothy M.
Published in Journal of pediatric surgery (01.03.2020)
Published in Journal of pediatric surgery (01.03.2020)
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Journal Article
Excess folic acid intake increases DNA de novo point mutations
Cao, Xuanye, Xu, Jianfeng, Lin, Ying L., Cabrera, Robert M., Chen, Qiuying, Zhang, Chaofan, Steele, John W., Han, Xiao, Gross, Steven S., Wlodarczyk, Bogdan J., Lupski, James R., Li, Wei, Wang, Hongyan, Finnell, Richard H., Lei, Yunping
Published in Cell discovery (28.02.2023)
Published in Cell discovery (28.02.2023)
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