The Application of Human iPSCs in Neurological Diseases: From Bench to Bedside

nork Xie, Nina, Tang, Beisha
Argitaratua izan da Stem Cells Int (2016)

DNA methylation and hydroxymethylation in stem cells

nork Cheng, Ying, Xie, Nina, Jin, Peng, Wang, Tao
Argitaratua izan da Cell Biochem Funct (2015)

Induced Pluripotent Stem Cells: Generation Strategy and Epigenetic Mystery behind Reprogramming

nork Ji, Pengfei, Manupipatpong, Sasicha, Xie, Nina, Li, Yujing
Argitaratua izan da Stem Cells Int (2016)

Long non-coding RNA MEG3 inhibits the proliferation and metastasis of oral squamous cell carcinoma by regulating the WNT/β-catenin signaling pathway

nork Liu, Zongxiang, Wu, Cui, Xie, Nina, Wang, Penglai
Argitaratua izan da Oncol Lett (2017)

Novel Epigenetic Techniques Provided by the CRISPR/Cas9 System

nork Xie, Nina, Zhou, Yafang, Sun, Qiying, Tang, Beisha
Argitaratua izan da Stem Cells Int (2018)

N6-Methyladenosine in RNA and DNA: An Epitranscriptomic and Epigenetic Player Implicated in Determination of Stem Cell Fate

nork Ji, Pengfei, Wang, Xia, Xie, Nina, Li, Yujing
Argitaratua izan da Stem Cells Int (2018)

Non-coding RNA in Fragile X Syndrome and Converging Mechanisms Shared by Related Disorders

nork Zhou, Yafang, Hu, Yacen, Sun, Qiying, Xie, Nina
Argitaratua izan da Front Genet (2019)

Alzheimer’s Disease: From Genetic Variants to the Distinct Pathological Mechanisms

nork Sun, Qiying, Xie, Nina, Tang, Beisha, Li, Rena, Shen, Yong
Argitaratua izan da Front Mol Neurosci (2017)

Impact of cusp inclinations on dental fractures in cracked tooth syndrome model and relevant risk evaluation

nork Xie, Nina, Wang, Penglai, Wu, Cui, Song, Wenting, Wang, Wen, Liu, Zongxiang
Argitaratua izan da Exp Ther Med (2017)

Reactivation of FMR1 by CRISPR/Cas9-Mediated Deletion of the Expanded CGG-Repeat of the Fragile X Chromosome

nork Xie, Nina, Gong, He, Suhl, Joshua A., Chopra, Pankaj, Wang, Tao, Warren, Stephen T.
Argitaratua izan da PLoS One (2016)

Chorea-Acanthocytosis in a Chinese Family With a Pseudo-Dominant Inheritance Mode

nork Yi, Fang, Li, Wenwen, Xie, Nina, Zhou, Yafang, Xu, Hongwei, Sun, Qiying, Zhou, Lin
Argitaratua izan da Front Neurol (2018)

High clinical heterogeneity in a Chinese pedigree of retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations (RVCL-S)

nork Xie, Nina, Sun, Qiying, Yang, Jinxia, Zhou, Yangjie, Xu, Hongwei, Zhou, Lin, Zhou, Yafang
Argitaratua izan da Orphanet J Rare Dis (2021)

NOTCH3 Variants and Genotype-Phenotype Features in Chinese CADASIL Patients

nork Hu, Yacen, Sun, Qiying, Zhou, Yafang, Yi, Fang, Tang, Haiyun, Yao, Lingyan, Tian, Yun, Xie, Nina, Luo, Mengchuan, Wang, Zhiqin, Liao, Xinxin, Xu, Hongwei, Zhou, Lin
Argitaratua izan da Front Genet (2021)

A recurrent 8 bp frameshifting indel in FOXF1 defines a novel mutation hotspot associated with alveolar capillary dysplasia with misalignment of pulmonary veins

nork Karolak, Justyna A., Bacolla, Albino, Liu, Qian, Lantz, Patrick E., Petty, John, Trapane, Pamela, Panzer, Karin, Totapally, Balagangadhar R., Niu, Zhiyv, Xiao, Rui, Xie, Nina G., Wu, Lucia R., Szafranski, Przemyslaw, Zhang, David Yu, Stankiewicz, Paweł
Argitaratua izan da Am J Med Genet A (2019)

Highly Sensitive Blocker Displacement Amplification and Droplet Digital PCR Reveal Low-Level Parental FOXF1 Somatic Mosaicism in Families with Alveolar Capillary Dysplasia with Mis...

nork Karolak, Justyna A., Liu, Qian, Xie, Nina G., Wu, Lucia R., Rocha, Gustavo, Fernandes, Susana, Ho-Ming, Luk, Lo, Ivan F., Mowat, David, Fiorino, Elizabeth K., Edelman, Morris, Fox, Joyce, Hayes, Denise A., Witte, David, Parrott, Ashley, Popek, Edwina, Szafranski, Przemyslaw, Zhang, David Y., Stankiewicz, Pawel
Argitaratua izan da J Mol Diagn (2020)

Low-level parental somatic mosaic SNVs in exomes from a large cohort of trios with diverse suspected Mendelian conditions

nork Gambin, Tomasz, Liu, Qian, Karolak, Justyna A., Grochowski, Christopher M., Xie, Nina G., Wu, Lucia R., Yan, Yan Helen, Cao, Ye, Akdemir, Zeynep H. Coban, Wilson, Theresa A., Jhangiani, Shalini N., Chen, Ed, Eng, Christine M., Muzny, Donna, Posey, Jennifer E., Yang, Yaping, Zhang, David Y., Shaw, Chad, Liu, Pengfei, Lupski, James R., Stankiewicz, Paweł
Argitaratua izan da Genet Med (2020)

Partial loss of psychiatric risk gene miR-137 in mice causes repetitive behavior and impairs sociability and learning via increased Pde10a

nork Cheng, Ying, Wang, Zhi-Meng, Tan, Weiqi, Wang, Xiaona, Li, Yujing, Bai, Bing, Li, Yuxin, Zhang, Shuang-Feng, Yan, Hai-Liang, Chen, Zuo-Lun, Liu, Chang-Mei, Mi, Ting-Wei, Xia, Shuting, Zhou, Zikai, Liu, An, Tang, Gang-Bin, Liu, Cong, Dai, Zhi-Jie, Wang, Ying-Ying, Wang, Hong, Wang, Xusheng, Kang, Yunhee, Lin, Li, Chen, Zhenping, Xie, Nina, Sun, Qinmiao, Xie, Wei, Peng, Junmin, Chen, Dahua, Teng, Zhao-Qian, Jin, Peng
Argitaratua izan da Nat Neurosci (2018)