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Cancer Research|August 17, 2006
Wilms' tumor 1 and signal transducers and activators of transcription 3 synergistically promote cell proliferation: a possible mechanism in sporadic Wilms' tumorYu Rong, Long Cheng, Hongxiu Ning, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|June 14, 2013
Association between PTCH1 polymorphisms and risk of neural tube defects in a Chinese populationZhen Wang, Li Wang, Shaofang Shangguan, et al.
BMC Pediatrics|March 4, 2023
A mosaic karyotype of 45,X/46,X,psu idic(Y)(q12) in a ten-year-old boy: integrating high-throughput sequencing with cytogenetic technique for precise diagnosis and genetic counsellingHui Yin, Hua Xie, Jizhen Zou, et al.
The American Journal of Clinical Nutrition|February 19, 2010
Relation between hypomethylation of long interspersed nucleotide elements and risk of neural tube defectsLi Wang, Fang Wang, Jing Guan, et al.
Genes & Nutrition|August 7, 2013
PCMT1 gene polymorphisms, maternal folate metabolism, and neural tube defects: a case-control study in a population with relatively low folate intakeFang Wang, Jianhua Wang, Jin Guo, et al.
Scientific Reports|November 3, 2017
Sporadic Hirschsprung Disease: Mutational Spectrum and Novel Candidate Genes Revealed by Next-generation SequencingZhen Zhang, Qi Li, Mei Diao, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|July 20, 2010
Global DNA hypomethylation is associated with NTD-affected pregnancy: A case-control studyXiaoli Chen, Jin Guo, Yunping Lei, et al.
Frontiers in Pediatrics|June 13, 2025
Comparison of efficacy of exosomes derived from human umbilical cord blood mesenchymal stem cells in treating mouse acute lung injury via different routesJing Chen, Shuang Liu, Jizhen Zou, et al.
Human Molecular Genetics|December 10, 2021
Antisense oligonucleotides targeting the SMN2 promoter region enhance SMN2 expression in spinal muscular atrophy cell lines and mouse modelJia Wang, Jinli Bai, Shijia OuYang, et al.
Metabolic Brain Disease|November 30, 2011
Glutamate carboxypeptidase II gene polymorphisms and neural tube defects in a high-risk Chinese populationHua Xie, Jin Guo, Jianhua Wang, et al.
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