Bilaketaren emaitzak - Geng, Juan

Deoxycholic acid induces the overexpression of intestinal mucin, MUC2, via NF-kB signaling pathway in human esophageal adenocarcinoma cells nork Wu, JianTao, Gong, Jun, Geng, Juan, Song, YinXue

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Identification of Key Proteins and Networks Related to Grain Development in Wheat (Triticum aestivum L.) by Comparative Transcription and Proteomic Analysis of Allelic Variants in... nork Du, Dengfeng, Gao, Xin, Geng, Juan, Li, Qingyan, Li, Liqun, Lv, Qian, Li, Xuejun

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Clinical Application of Chromosome Microarray Analysis in Han Chinese Children with Neurodevelopmental Disorders nork Xu, Mingyu, Ji, Yiting, Zhang, Ting, Jiang, Xiaodong, Fan, Yun, Geng, Juan, Li, Fei

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A novel 1p33p32.2 deletion involving SCP2, ORC1, and DAB1 genes in a patient with craniofacial dysplasia, short stature, developmental delay, and leukoencephalopathy: A case report nork Jiang, Maoying, Wang, Shanlin, Li, Fei, Geng, Juan, Ji, Yiting, Li, Ke, Jiang, Xiaodong

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A modified multiplex ligation-dependent probe amplification method for the detection of 22q11.2 copy number variations in patients with congenital heart disease nork Zhang, Xiaoqing, Xu, Yuejuan, Liu, Deyuan, Geng, Juan, Chen, Sun, Jiang, Zhengwen, Fu, Qihua, Sun, Kun

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Tunable Band-Stop Filters for Graphene Plasmons Based on Periodically Modulated Graphene nork Shi, Bin, Cai, Wei, Zhang, Xinzheng, Xiang, Yinxiao, Zhan, Yu, Geng, Juan, Ren, Mengxin, Xu, Jingjun

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Combined transcriptome and proteome analyses reveal differences in the longissimus dorsi muscle between Kazakh cattle and Xinjiang brown cattle nork Yan, XiangMin, Wang, Jia, Li, Hongbo, Gao, Liang, Geng, Juan, Ma, Zhen, Liu, Jianming, Zhang, Jinshan, Xie, Penggui, Chen, Lei

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New sonographic feature (C‐sign) to improve the prenatal accuracy of jejunal atresia nork Chen, Dan, Tam, Kwong Ho, Xiao, Yiwei, Geng, Juan, Tan, Yu, Zhu, Xiaochun, Ge, Wuping, Zhou, Jialiang, Xiao, Shangjie, Chen, Jiaxin

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SORBS2 is a genetic factor contributing to cardiac malformation of 4q deletion syndrome patients nork Liang, Fei, Wang, Bo, Geng, Juan, You, Guoling, Fa, Jingjing, Zhang, Min, Sun, Hunying, Chen, Huiwen, Fu, Qihua, Zhang, Xiaoqing, Zhang, Zhen

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Estrogen Attenuates Chronic Stress-Induced Cardiomyopathy by Adaptively Regulating Macrophage Polarizations via β(2)-Adrenergic Receptor Modulation nork Hou, Hongjian, Adzika, Gabriel Komla, Wu, Qi, Ma, Tongtong, Ma, Yanhong, Geng, Juan, Shi, Mingjin, Fu, Lu, Rizvi, Ruqayya, Gong, Zheng, Sun, Hong

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Screening for Coding Variants in FTO and SH2B1 Genes in Chinese Patients with Obesity nork Zheng, Zhaojing, Hong, Li, Huang, Xiaodong, Yang, Peirong, Li, Juan, Ding, Yu, Yao, Ru-en, Geng, Juan, Shen, Yongnian, Shen, Yiping, Fu, Qihua, Yu, Yongguo

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The incubation period of COVID-19: a global meta-analysis of 53 studies and a Chinese observation study of 11 545 patients nork Cheng, Cheng, Zhang, DongDong, Dang, Dejian, Geng, Juan, Zhu, Peiyu, Yuan, Mingzhu, Liang, Ruonan, Yang, Haiyan, Jin, Yuefei, Xie, Jing, Chen, Shuaiyin, Duan, Guangcai

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Estrogen regulation of cardiac cAMP-L-type Ca(2+) channel pathway modulates sex differences in basal contraction and responses to β(2)AR-mediated stress in left ventricular apical... nork Machuki, Jeremiah Ong’achwa, Zhang, Hong-Yuan, Geng, Juan, Fu, Lu, Adzika, Gabriel Komla, Wu, Lijuan, Shang, Wenkang, Wu, Jinxia, Kexue, Li, Zhao, Zhiwei, Sun, Hong

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A Novel Variant in CDKN1C Is Associated With Intrauterine Growth Restriction, Short Stature, and Early-Adulthood-Onset Diabetes nork Kerns, Sarah L., Guevara-Aguirre, Jaime, Andrew, Shayne, Geng, Juan, Guevara, Carolina, Guevara-Aguirre, Marco, Guo, Michael, Oddoux, Carole, Shen, Yiping, Zurita, Andres, Rosenfeld, Ron G., Ostrer, Harry, Hwa, Vivian, Dauber, Andrew

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Chromosome microarray testing for patients with congenital heart defects reveals novel disease causing loci and high diagnostic yield nork Geng, Juan, Picker, Jonathan, Zheng, Zhaojing, Zhang, Xiaoqing, Wang, Jian, Hisama, Fuki, Brown, David W, Mullen, Mary P, Harris, David, Stoler, Joan, Seman, Ann, Miller, David T, Fu, Qihua, Roberts, Amy E, Shen, Yiping

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A New Subtype of Multiple Synostoses Syndrome Is Caused by a Mutation in GDF6 That Decreases Its Sensitivity to Noggin and Enhances Its Potency as a BMP Signal nork Wang, Jian, Yu, Tingting, Wang, Zhigang, Ohte, Satoshi, Yao, Ru-en, Zheng, Zhaojing, Geng, Juan, Cai, Haiqing, Ge, Yihua, Li, Yuchan, Xu, Yunlan, Zhang, Qinghua, Gusella, James F, Fu, Qihua, Pregizer, Steven, Rosen, Vicki, Shen, Yiping

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