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Annals of Neurology|August 21, 2016
A recurrent mutation in KCNA2 as a novel cause of hereditary spastic paraplegia and ataxiaKatherine L Helbig, Ulrike B S Hedrich, Deepali N Shinde, et al.
Oncotarget|May 15, 2018
TumorNext-Lynch-MMR: a comprehensive next generation sequencing assay for the detection of germline and somatic mutations in genes associated with mismatch repair deficiency and Lynch syndromePhillip N Gray, Pei Tsai, Daniel Chen, et al.
Cancer Causes & Control : CCC|August 26, 2009
Human papillomavirus type-distribution in cervical cancer in China: the importance of HPV 16 and 18Wen Chen, Xun Zhang, Anco Molijn, et al.
Neuro-Oncology Advances|January 16, 2026
Preclinical assessment of checkpoint blockade combined with DNA methyltransferase inhibition in high-risk pediatric brain tumors reveals limited therapeutic synergyDeepak Kumar Mishra, Shelli M Morris, Dean Popovski, et al.
Lipids in Health and Disease|December 28, 2024
Familial hypercholesterolemia in Chinese children and adolescents: a multicenter studyMeng-Na Huang, Chen-Cen Wang, Ming-Sheng Ma, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|December 1, 2022
Promotion of Lung Cancer Metastasis by SIRT2-Mediated Extracellular Protein DeacetylationMeng Wu, Jian-Bin Zhang, Yi-Wei Xiong, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 16, 2009
A proprotein convertase subtilisin/kexin type 9 neutralizing antibody reduces serum cholesterol in mice and nonhuman primatesJoyce C Y Chan, Derek E Piper, Qiong Cao, et al.
Asian Pacific Journal of Cancer Prevention : APJCP|May 20, 2015
Establishing a Nomogram for Stage IA-IIB Cervical Cancer Patients after Complete ResectionHang Zhou, Xiong Li, Yuan Zhang, et al.
Acta Neuropathologica|December 11, 2019
Pineoblastoma segregates into molecular sub-groups with distinct clinico-pathologic features: a Rare Brain Tumor Consortium registry studyBryan K Li, Alexandre Vasiljevic, Christelle Dufour, et al.
European Journal of Human Genetics : EJHG|June 30, 2016
Loss of function of the retinoid-related nuclear receptor (RORB) gene and epilepsyGabrielle Rudolf, Gaetan Lesca, Mana M Mehrjouy, et al.
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