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Frontiers in Neurology|July 5, 2021
Case Report: Clinical Features of Childhood Leukoencephalopathy With Cerebral Calcifications and Cysts Due to SNORD118 VariantsHong Jin, Xiaotun Ren, Husheng Wu, et al.
Frontiers in Genetics|May 3, 2021
Novel Intronic Mutations Introduce Pseudoexons in DMD That Cause Muscular Dystrophy in PatientsXinguo Lu, Chunxi Han, Jiahui Mai, et al.
Microscopy and Microanalysis : the Official Journal of Microscopy Society of America, Microbeam Analysis Society, Microscopical Society of Canada|February 25, 2014
Sample preparation to observe the straight and flat posture of silkworm embryo under scanning electron microscopy via glycerol substitution methodWenbin Liu, Chenzhao Li, Qi Zhang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|May 11, 2021
[Clinical and genetic analysis of a patient with Mowat-Wilson syndrome]Pingli Zhang, Yanqi Hou, Peiyuan Liao, et al.
Frontiers in Oncology|October 9, 2023
Choice of radiotherapy modality for the combined treatment of non-small cell lung cancer with brain metastases: whole-brain radiation therapy with simultaneous integrated boost or stereotactic radiosurgeryXiaotao Dong, Kunlun Wang, Hui Yang, et al.
Frontiers in Endocrinology|November 13, 2023
The Nomogram predicting the overall survival of patients with pancreatic cancer treated with radiotherapy: a study based on the SEER database and a Chinese cohortXiaotao Dong, Kunlun Wang, Hui Yang, et al.
Science Advances|October 5, 2022
The linker domain of the initiator DnaA contributes to its ATP binding and membrane association in E. coli chromosomal replicationYanqi Hou, Pankaj Kumar, Monika Aggarwal, et al.
Cell & Bioscience|October 30, 2025
IgD in nucleus of pro-B cells promotes pro-B cells proliferation by regulating E2F3 expressionYixiao Zhang, Yanqi Hou, Meng Yu, et al.
European Journal of Medical Genetics|February 2, 2021
Novel truncating mutations in ASXL1 identified in two boys with Bohring-Opitz syndromeJianbo Zhao, Yanqi Hou, Fang Fang, et al.
Frontiers in Pediatrics|November 16, 2020
Mutant BCL11B in a Patient With a Neurodevelopmental Disorder and T-Cell AbnormalitiesSai Yang, Qingyun Kang, Yanqi Hou, et al.
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