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Yong-guo Zhang,Yinglin Xia,Jun Sun(Division of Gastroenterology and Hepatology;UIC Cancer Center;Department of Microbiology and Immunology).A simple and sensitive method to detect vitamin D receptor expression in various disease models using stool samples[J].基因与疾病(英文),2021,第6期
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Qin Zhou,Hao Xu,Liang Yan,Liang Ye,Xinyuan Zhang,Bin Tan,Qin Yi,Jie Tian,Jing Zhu(Department of Pediatric Research Institute;Chongqing Key Laboratory of Pediatrics;Department of Clinical Laboratory Ministry of Education Key Laboratory of Child Development and Disorders National Clinical Research Center for Child Health and Disorders(Chongqing)China International Science and Technology Cooperation Base of Child Development and Critical Disorders Children’s Hospital of Chongqing Medical University;Department of Cardiovascular(Internal Medicine);Chengdu Women’s and Children’s Central Hospital).PGC-1α promotes mitochondrial respiration and biogenesis during the differentiation of hiPSCs into cardiomyocytes[J].基因与疾病(英文),2021,第6期
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Yanping Wang,Qiuyun Yang,Xuemei Chen,Wenjing Tang,Lina Zhou,Zhi Chen,Yunfei An,Zhiyong Zhang,Xuemei Tang,Xiaodong Zhao(National Clinical Research Center for Child Health and Disorders(Chongqing);China International Science and Technology Cooperation Base of Child Development and Critical Disorders;Chongqing Key Laboratory of Child Infection and Immunity;Division of Rheumatology and Immunology).Phenotypic characterization of patients with activated PI3Kδ syndrome 1 presenting with features of systemic lupus erythematosus[J].基因与疾病(英文),2021,第6期
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Waqar Ahmad,Paul R.Ebert(School of Biological Sciences).Suppression of a core metabolic enzyme dihydrolipoamide dehydrogenase (dld ) protects against amyloid beta toxicity in C.elegans model of Alzheimer’s disease[J].基因与疾病(英文),2021,第6期
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Beijian Zhang,Hao Jiang,Zhen Dong,Aijun Sun,Junbo Ge(Department of Cardiology;Shanghai Institute of Cardiovascular Diseases;Institutes of Biomedical Sciences;NHC Key Laboratory of Viral Heart Diseases;Key Laboratory of Viral Heart Diseases).The critical roles of m6A modification in metabolic abnormality and cardiovascular diseases[J].基因与疾病(英文),2021,第6期
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Yichen Liu,Qiong Zhao,Tao Xi,Lufeng Zheng,Xiaoman Li(Jiangsu Key Laboratory for Pharmacology and Safety Evaluation of Chinese Materia Medica;School of Life Science and Technology).MicroRNA-9 as a paradoxical but critical regulator of cancer metastasis:Implications in personalized medicine[J].基因与疾病(英文),2021,第6期
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Xingxing Huang,Ting Pan,Lili Yan,Ting Jin,Ruonan Zhang,Bi Chen,Jiao Feng,Ting Duan,Yu Xiang,Mingming Zhang,Xiaying Chen,Zuyi Yang,Wenzheng Zhang,Xia Ding,Tian Xie,Xinbing Sui(Department of Medical Oncology;College of Pharmacy;Key Laboratory of Elemene Class Anti-Cancer Chinese Medicines;School of Traditional Chinese Medicine).The inflammatory microenvironment and the urinary microbiome in the initiation and progression of bladder cancer[J].基因与疾病(英文),2021,第6期
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Mariaelena Valentino,Elisabetta Dejana,Matteo Malinverno(The FIRC Institute of Molecular Oncology(IFOM);Department of Oncology and Haemato-Oncology;Vascular Biology).The multifaceted PDCD10/CCM3 gene[J].基因与疾病(英文),2021,第6期
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Xiaoguang Liu,Yilei Zhang,Li Zhuang,Kellen Olszewski,Boyi Gan(Department of Experimental Radiation Oncology;Kadmon Corporation;The University of Texas).NADPH debt drives redox bankruptcy:SLC7A11/xCT-mediated cystine uptake as a double-edged sword in cellular redox regulation[J].基因与疾病(英文),2021,第6期
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Yukun Mao,Na Ni,Linjuan Huang,Jiaming Fan,Hao Wang,Fang He,Qing Liu,Deyao Shi,Kai Fu,Mikhail Pakvasa,William Wagstaff,Andrew Blake Tucker,Connie Chen,Russell R.Reid,Rex C.Haydon,Sherwin H.Ho,Michael J.Lee,Tong-Chuan He,Jian Yang,Le Shen,Lin Cai,Hue H.Luu(Departments of Spine Surgery and Musculoskeletal Tumor;Molecular Oncology Laboratory;Ministry of Education Key Laboratory of Diagnostic Medicine;Departments of Nephrology;Department of Spine Surgery;Department of Orthopaedic Surgery;Section of Plastic Surgery and Laboratory of Craniofacial Biology and Development;Department of Biomedical Engineering).Argonaute(AGO)proteins play an essential role in mediating BMP9-induced osteogenic signaling in mesenchymal stem cells(MSCs)[J].基因与疾病(英文),2021,第6期
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Jian Chen,Biao Luo,Bi-Rou Zhong,Kun-Yi Li,Qi-Xin Wen,Li Song,Xiao-Jiao Xiang,Gui-Feng Zhou,Li-Tian Hu,Xiao-Juan Deng,Yuan-Lin Ma,Guo-Jun Chen(Department of Neurology;Department of Neurology).Sulfuretin exerts diversified functions in the processing of amyloid precursor protein[J].基因与疾病(英文),2021,第6期
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Yi Pan,Qingshang Li,Zhijun Cao,Shuliang Zhao(Division of Gastroenterology and Hepatology).The SUMO E3 ligase CBX4 is identified as a poor prognostic marker of gastric cancer through multipronged OMIC analyses[J].基因与疾病(英文),2021,第6期
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Chao Li,Shang-Ze Li,Xi-Cheng Huang,Jie Chen,Wenbin Liu,Xiao-Dong Zhang,Xue-Min Song,Run-Lei Du(Research Centre of Anesthesiology and Critical Care Medicine;Hubei Key Laboratory of Cell Homeostasis;College of Health Sciences and Nursing).PTPN18 promotes colorectal cancer progression by regulating the c-MYC-CDK4 axis[J].基因与疾病(英文),2021,第6期
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Dongwei Fan,Daoyang Fan,Wanqiong Yuan(Department of Orthopedics;Beijing Key Laboratory of Spinal Disease).CMTM3 suppresses bone formation and osteogenic differentiation of mesenchymal stem cells through inhibiting Erk1/2 and RUNX2 pathways[J].基因与疾病(英文),2021,第6期
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Hui Nie,Zhujun Liao,Yutong Wang,Jianhua Zhou,Xiaoyun He,Chunlin Ou(Department of Pathology;Department of Rheumatology and Immunology;National Clinical Research Center for Geriatric Disorders).Exosomal long non-coding RNAs:Emerging players in cancer metastasis and potential diagnostic biomarkers for personalized oncology[J].基因与疾病(英文),2021,第6期
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Xudong Peng,Guangyi Liu,Hongxia Peng,Anqi Chen,Lang Zha,Ziwei Wang(Gastrointestinal Surgical Unit;Department of General Surgery).Corrigendum to“SOX4 contributions to TGFb-induced endothelial-mesenchymal transition and stem cell characteristics of gastric cancer cells”[Genes&Diseases 5(2018)49e61][J].基因与疾病(英文),2021,第6期
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Xiaoxing Wu,Zhaoxia Li,Hongyu Zhang,Fang He,Min Qiao,Huaxiu Luo,Jing Zhang,Meng Zhang,Yukun Mao,William Wagstaff,Yongtao Zhang,Changchun Niu,Xia Zhao,Hao Wang,Linjuan Huang,Deyao Shi,Qing Liu,Na Ni,Kai Fu,Rex C.Haydon,Russell R.Reid,Hue H.Luu,Tong-Chuan He,Ziwei Wang,Houjie Liang,Bing-Qiang Zhang,Ning Wang(Departments of Gastrointestinal Surgery;Molecular Oncology Laboratory;Department of Oncology;Departments of Burn&Plastic Surgery;Department of Orthopaedic Surgery;Departments of Orthopaedic Surgery;Department of Orthopaedic Surgery;Department of Clinical Laboratory Medicine;Ministry of Education Key Laboratory of Diagnostic Medicine;Department of Orthopaedics;Department of Spine Surgery;Department of Oncology and Southwest Cancer Center).Modeling colorectal tumorigenesis using the organoids derived from conditionally immortalized mouse intestinal crypt cells (ciMICs)[J].基因与疾病(英文),2021,第6期
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Xiaoxing Wu,Bin Peng,Kun Qian,Wei Zhang,Jiang Min,Mingjun Zhang,Fanling Zeng,Ziwei Wang(Department of Gastrointestinal Surgery;School of Public Health and Management;Health Management Center).The combination of methylenehydrofolate reductase C677T polymorphism screening and gastrointestinal tumor markers detection may be an early screening method for gastrointestinal cancer related to helicobacter pylori infection[J].基因与疾病(英文),2021,第6期
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Jilei Zhang,Yinglin Xia,Jun Sun(Division of Gastroenterology and Hepatology).Breast and gut microbiome in health and cancer[J].基因与疾病(英文),2021,第5期
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Wenjie Zhong,Huaxiang Zhao,Wenbin Huang,Mengqi Zhang,Qian Zhang,Yue Zhang,Chong Chen,Zulihumaer Nueraihemaiti,Dilifeire Tuerhong,Huizhe Huang,Gulibaha Maimaitili,Feng Chen,Jiuxiang Lin(Department of Orthodontics;Central Laboratory;Department of Stomatology;Xinjiang Medical University;Chongqing Medical University;Key Laboratory of Shaanxi Province for Craniofacial Precision Medicine Research;Department of Orthodontics).Identification of rare PTCH1 nonsense variant causing orofacial cleft in a Chinese family and an up-to-date genotype- phenotype analysis[J].基因与疾病(英文),2021,第5期
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Cheng-Long Huang,Liu-Ling Xiao,Min Xu,Jun Li,Shu-Fen Li,Cui-Song Zhu,Yu-Li Lin,Rui He,Xi Li(Biology Science Institutes;Center for Translational Research in Hematologic Malignancies;Key Laboratory of Metabolic Molecular Medicine;Shanghai Public Health Clinical Center;Department of Immunology).Chemerin deficiency regulates adipogenesis is depot different through TIMP1[J].基因与疾病(英文),2021,第5期
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Yanze Yin,Defu Kong,Kang He,Qiang Xia(Department of Liver Surgery;Department of Hepatology&Gastroenterology).Regeneration and activation of liver progenitor cells in liver cirrhosis[J].基因与疾病(英文),2021,第5期
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Vellingiri Balachandar,Kamarajan Rajagopalan,Kaavya Jayaramayya,Madesh Jeevanandam,Mahalaxmi Iyer(Human Molecular Genetics and Stem Cell Laboratory;Department of Zoology;Department of Biochemistry).Mitochondrial dysfunction:A hidden trigger of autism?[J].基因与疾病(英文),2021,第5期
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Weilin Zhang(State Key Laboratory of Membrane Biology).The mitophagy receptor FUN14 domaincontaining 1 (FUNDC1):A promising biomarker and potential therapeutic target of human diseases[J].基因与疾病(英文),2021,第5期
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Daopei Zou,Yangmei Chen,Lingzhao Zhang,Xiaohui Yuan,Yujie Zhang,Adelina Inggawati,Pham Thi Kieu Nguyet,Tianwen Gao,Jin Chen(Department of Dermatology;Key Laboratory of Clinical Laboratory Diagnostics;Department of Dermatology).SFRP5 inhibits melanin synthesis of melanocytes in vitiligo by suppressing the Wnt/b-catenin signaling[J].基因与疾病(英文),2021,第5期
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Fengji Liang,Yuan Quan,Andong Wu,Ying Chen,Ruifeng Xu,Yuexing Zhu,Jianghui Xiong(Lab of Epigenetics and Advanced Health Technology;State Key Laboratory of Space Medicine Fundamentals and Application;School of Computer Science and Technology).Insulin-resistance and depression cohort data mining to identify nutraceutical related DNA methylation biomarker for type 2 diabetes[J].基因与疾病(英文),2021,第5期
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Yu Zhang,Guoyong Zhang,Wenhui Chen,Zheng Pu,Lu Song,Xinghua Tang,Zhenguo Liu(Department of Neurology).A novel ABCD1 G1202A mutation in a Chinese patient with pure adrenomyeloneuropathy and literature review[J].基因与疾病(英文),2021,第5期
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Haoyue Xu,Hang Liu,Tao Chen,Bo Song,Jin Zhu,Xing Liu,Ming Li,Cong Luo(Department of Orthopedic;Department of Pathology;Molecular Oncology Laboratory).The R168G heterozygous mutation of tropomyosin 3 (TPM3) was identified in three family members and has manifestations ranging from asymptotic to serve scoliosis and respiratory complications[J].基因与疾病(英文),2021,第5期
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Lu Yang,Xiuhong Xue,Xuemei Chen,Junfeng Wu,Xi Yang,Li Xu,Xuemei Tang,Mo Wang,Huawei Mao,Xiaodong Zhao(Chongqing Key Laboratory of Child Infection and Immunity;Department of Rheumatology and Immunology;Department of Internal Nephrology;Ministry of Education Key Laboratory of Child Development and Disorders).Abatacept is effective in Chinese patients with LRBA and CTLA4 deficiency[J].基因与疾病(英文),2021,第5期
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Saurav Bhaskar Saha,Vijai Kumar Gupta,Pramod Wasudeo Ramteke(Department of Computational Biology and Bioinformatics;Department of Chemistry and Biotechnology;Department of Biological Sciences;AgroBioSciences(AgBS)and Chemical&Biochemical Sciences(CBS)Department).uCARE Chem Suite and uCAREChemSuiteCLI:Tools for bacterial resistome prediction[J].基因与疾病(英文),2021,第5期
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