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Cancer Research|February 12, 2005
Folate transport gene inactivation in mice increases sensitivity to colon carcinogenesisDavid W L Ma, Richard H Finnell, Laurie A Davidson, et al.
Journal of Medicinal Chemistry|April 10, 2019
Galloyl Carbohydrates with Antiangiogenic Activity Mediated by Capillary Morphogenesis Gene 2 (CMG2) Protein BindingElisa G-Doyagüez, Paula Carrero, Andrés Madrona, et al.
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.
Developmental Cell|June 29, 2013
Fuz mutant mice reveal shared mechanisms between ciliopathies and FGF-related syndromesJacqueline M Tabler, William B Barrell, Heather L Szabo-Rogers, 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 Slc25a32Jimi Kim, Yunping Lei, Jin Guo, et al.
The Journal of Clinical Investigation|April 29, 2010
Folate regulation of axonal regeneration in the rodent central nervous system through DNA methylationBermans J Iskandar, Elias Rizk, Brenton Meier, et al.
Neurology|March 23, 2005
Cerebral folate deficiency with developmental delay, autism, and response to folinic acidP Moretti, T Sahoo, K Hyland, et al.
Human Mutation|September 2, 2022
CIC missense variants contribute to susceptibility for spina bifidaXiao Han, Xuanye Cao, Vanessa Aguiar-Pulido, et al.
Journal of Stroke and Cerebrovascular Diseases : the Official Journal of National Stroke Association|December 29, 2016
Higher Stroke Risk with Lower Blood Pressure in Hemodynamic Vertebrobasilar Disease: Analysis from the VERiTAS StudySepideh Amin-Hanjani, Tanya N Turan, Xinjian Du, et al.
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