Bibliotecas PUC-SP - Busca Integrada

Further delineation of phenotype and genotype of Kenny–Caffey syndrome type 2 (phenotype and genotype of KCS type 2)

Autor Xuefei Chen, Chaochun Zou
Vydáno v Molecular Genetics & Genomic Medicine (2024-04-01)

Clinical manifestations in a Chinese girl with heterozygous de novo NAA10 variant c. 247C > T, p. (Arg83Cys): a case report

Autor Kaiyan Wei, Chaochun Zou
Vydáno v Frontiers in Pediatrics (2023-06-01)

The Clinical and Genetic Characteristics in Children with Idiopathic Hypogonadotropin Hypogonadism

Autor Qiong Zhou, Wenbin Sheng, Suhong Yang, Chaochun Zou
Vydáno v Journal of Oncology (2022-01-01)

Hereditary nonspherocytic hemolytic anemia caused by glucose-6-phosphate isomerase (GPI) deficiency in a Chinese patient: a case report

Autor Yumei Zu, Hui Wang, Weijia Lin, Chaochun Zou
Vydáno v BMC Pediatrics (2022-08-01)

Microdeletion of 4p16.2 in Children: A Case Report and Literature Review

Autor Yanjie Qian, Xiaoying Wang, Wei Tang, Chaochun Zou
Vydáno v Case Reports in Genetics (2022-01-01)

Genotype–Phenotype Correlations in Angelman Syndrome

Autor Lili Yang, Xiaoli Shu, Shujiong Mao, Yi Wang, Xiaonan Du, Chaochun Zou
Vydáno v Genes (2021-06-01)

Severe Adenovirus Pneumonia Requiring Extracorporeal Membrane Oxygenation Support in Immunocompetent Children

Autor Xuefei Chen, Jianhai Lv, Jianhai Lv, Lu Qin, Chaochun Zou, Lanfang Tang
Vydáno v Frontiers in Pediatrics (2020-04-01)

Antenatal exposure to betamethasone induces placental 11β-hydroxysteroid dehydrogenase type 2 expression and the adult metabolic disorders in mice.

Autor Li Ni, Yibin Pan, Chao Tang, Wenyi Xiong, Ximei Wu, Chaochun Zou
Vydáno v PLoS ONE (2018-01-01)

Do patients with Prader–Willi syndrome have favorable glucose metabolism?

Autor Yanjie Qian, Fangling Xia, Yiming Zuo, Mianling Zhong, Lili Yang, Yonghui Jiang, Chaochun Zou
Vydáno v Orphanet Journal of Rare Diseases (2022-05-01)

Perinatal features of Prader-Willi syndrome: a Chinese cohort of 134 patients

Autor Lili Yang, Qiong Zhou, Bo Ma, Shujiong Mao, Yanli Dai, Mingqiang Zhu, Chaochun Zou
Vydáno v Orphanet Journal of Rare Diseases (2020-01-01)

Regulatory roles and mechanisms of alternative RNA splicing in adipogenesis and human metabolic health

Autor Yunqi Chao, Yonghui Jiang, Mianling Zhong, Kaiyan Wei, Chenxi Hu, Yifang Qin, Yiming Zuo, Lili Yang, Zheng Shen, Chaochun Zou
Vydáno v Cell & Bioscience (2021-04-01)

Vitamin C deficiency induces hypoglycemia and cognitive disorder through S-nitrosylation-mediated activation of glycogen synthase kinase 3β

Autor Yingying Shu, Chaochun Zou, Yuqing Cai, Qiangqiang He, Xiaowei Wu, Haibin Zhu, Meiyu Qv, Yunqi Chao, Chengyun Xu, Lanfang Tang, Ximei Wu
Vydáno v Redox Biology (2022-10-01)

Metabolic profiling reveals altered amino acid and fatty acid metabolism in children with Williams Syndrome

Autor Weijun Chen, Yang Yang, Yu Zhang, Changxuan Sun, Chai Ji, Jiyang Shen, Fangfang Li, Yingping Xiao, Yang Wen, Qian Liu, Chaochun Zou
Vydáno v Scientific Reports (2024-12-01)

Health-related quality of life of children with Williams syndrome and caregivers in China

Autor Weijun Chen, Lidan Sun, Xinyu He, Ziqiao Li, Chai Ji, Fangfang Li, Jiyang Shen, Tianxin Pan, Xuejing Jin, Yusang Dong, Lidan Hu, Chaochun Zou, Guannan Bai
Vydáno v Frontiers in Public Health (2023-06-01)

Using sno-lncRNAs as potential markers for Prader-Willi syndrome diagnosis

Autor Jiu-Ru Sun, Liang-Zhong Yang, Yang-Li Dai, Huang Wu, Siqi Li, Yi-Feng Xu, Youkui Huang, Hao Wu, Zheng Shen, Chaochun Zou, Ling-Ling Chen
Vydáno v RNA Biology (2023-12-01)

Phosphorylation of human glioma-associated oncogene 1 on Ser937 regulates Sonic Hedgehog signaling in medulloblastoma

Autor Ling-Hui Zeng, Chao Tang, Minli Yao, Qiangqiang He, Meiyu Qv, Qianlei Ren, Yana Xu, Tingyu Shen, Weizhong Gu, Chengyun Xu, Chaochun Zou, Xing Ji, Ximei Wu, Jirong Wang
Vydáno v Nature Communications (2024-02-01)