New Techniques for the Study of Neural Tube Defects

por Lei, Yunping, Finnell, Richard H
Publicado 2015

Organoids as a new model system to study neural tube defects

por Wu, Yu, Peng, Sisi, Finnell, Richard H., Zheng, Yufang
Publicado 2021

Pax3 lineage-specific deletion of Gpr161 is associated with spinal neural tube and craniofacial malformations during embryonic development

por Kim, Sung-Eun, Chothani, Pooja J., Shaik, Rehana, Pollard, Westley, Finnell, Richard H.
Publicado 2023

Folic acid modifies the shape of epithelial cells during morphogenesis via a Folr1 and MLCK dependent mechanism

por Martin, Jessica B., Muccioli, Maria, Herman, Kenneth, Finnell, Richard H., Plageman, Timothy F.
Publicado 2019

Identification of Novel CELSR1 Mutations in Spina Bifida

por Lei, Yunping, Zhu, Huiping, Yang, Wei, Ross, M. Elizabeth, Shaw, Gary M., Finnell, Richard H.
Publicado 2014

Retinoic Acid-Dependent Signaling Pathways and Lineage Events in the Developing Mouse Spinal Cord

por Paschaki, Marie, Lin, Song-Chang, Wong, Rebecca Lee Yean, Finnell, Richard H., Dollé, Pascal, Niederreither, Karen
Publicado 2012

Whole-exome sequencing study of hypospadias

por Chen, Zhongzhong, Lei, Yunping, Finnell, Richard H., Ding, Yu, Su, Zhixi, Wang, Yaping, Xie, Hua, Chen, Fang
Publicado 2023

Association between CFL1 gene polymorphisms and spina bifida risk in a California population

por Zhu, Huiping, Enaw, James O Ebot, Ma, Chen, Shaw, Gary M, Lammer, Edward J, Finnell, Richard H
Publicado 2007

Whole genome microarray analysis, from neonatal blood cards

por Hardin, Jill, Finnell, Richard H, Wong, David, Hogan, Michael E, Horovitz, Joy, Shu, Jenny, Shaw, Gary M
Publicado 2009

Fuz Regulates Craniofacial Development through Tissue Specific Responses to Signaling Factors

por Zhang, Zichao, Wlodarczyk, Bogdan J., Niederreither, Karen, Venugopalan, Shankar, Florez, Sergio, Finnell, Richard H., Amendt, Brad A.
Publicado 2011

Mutations in Planar Cell Polarity Gene SCRIB Are Associated with Spina Bifida

por Lei, Yunping, Zhu, Huiping, Duhon, Cody, Yang, Wei, Ross, M. Elizabeth, Shaw, Gary M., Finnell, Richard H.
Publicado 2013

Autism-Like Behavior and Epigenetic Changes Associated with Autism as Consequences of In Utero Exposure to Environmental Pollutants in a Mouse Model

por Hill, Denise S., Cabrera, Robert, Wallis Schultz, Deeann, Zhu, Huiping, Lu, Wei, Finnell, Richard H., Wlodarczyk, Bogdan J.
Publicado 2015

Differentially expressed genes in embryonic cardiac tissues of mice lacking Folr1 gene activity

por Zhu, Huiping, Cabrera, Robert M, Wlodarczyk, Bogdan J, Bozinov, Daniel, Wang, Deli, Schwartz, Robert J, Finnell, Richard H
Publicado 2007

CHKA and PCYT1A gene polymorphisms, choline intake and spina bifida risk in a California population

por Enaw, James O Ebot, Zhu, Huiping, Yang, Wei, Lu, Wei, Shaw, Gary M, Lammer, Edward J, Finnell, Richard H
Publicado 2006

Epigenetic alterations in folate transport genes in placental tissue from fetuses with neural tube defects and in leukocytes from subjects with hyperhomocysteinemia

por Farkas, Sanja A., Böttiger, Anna K., Isaksson, Helena S., Finnell, Richard H., Ren, Aiguo, Nilsson, Torbjörn K., Nilsson, Torbjörn K.
Publicado 2013

Analysis of archived residual newborn screening blood spots after whole genome amplification

por Cantarel, Brandi L., Lei, Yunping, Weaver, Daniel, Zhu, Huiping, Farrell, Andrew, Benstead-Hume, Graeme, Reese, Justin, Finnell, Richard H.
Publicado 2015

MiR-302 Regulates Glycolysis to Control Cell-Cycle during Neural Tube Closure

por Keuls, Rachel A., Kojima, Karin, Lozzi, Brittney, Steele, John W., Chen, Qiuying, Gross, Steven S., Finnell, Richard H., Parchem, Ronald J.
Publicado 2020

KDM6B Variants May Contribute to the Pathophysiology of Human Cerebral Folate Deficiency

por Han, Xiao, Cao, Xuanye, Cabrera, Robert M., Pimienta Ramirez, Paula Andrea, Zhang, Cuilian, Ramaekers, Vincent T., Finnell, Richard H., Lei, Yunping
Publicado 2022

Genetic analysis of Wnt/PCP genes in neural tube defects

por Chen, Zhongzhong, Lei, Yunping, Cao, Xuanye, Zheng, Yufang, Wang, Fang, Bao, Yihua, Peng, Rui, Finnell, Richard H., Zhang, Ting, Wang, Hongyan
Publicado 2018

Combined effects of FH (E404D) and ACOX2 (R409H) cause metabolic defects in primary cardiac malignant tumor

por Zhou, Xiangyu, Xu, Mengjia, Zeng, Weijia, Chen, Zhongzhong, Lu, Guohui, Gong, Yun, Finnell, Richard H., Xiao, Huasheng, Qiao, Bin, Wang, Hongyan
Publicado 2018