Lin Chen

发表

CXCL12/CXCR4 axis promotes mesenchymal stem cell mobilization to burn wounds and contributes to wound repair.

Yahan Fan, Jiongyu Hu, Dong-xia Zhang, 2013, The Journal of surgical research.

VKORC1-1639G>A, CYP2C9, EPHX1691A>G genotype, body weight, and age are important predictors for warfarin maintenance doses in patients with mechanical heart valve prostheses in southwest China

Q. Zhong, Yingbin Xiao, J. Schneede, 2010, European Journal of Clinical Pharmacology.

Inactivation of Vhl in Osteochondral Progenitor Cells Causes High Bone Mass Phenotype and Protects Against Age‐Related Bone Loss in Adult Mice

Di Chen, Qifen He, F. Luo, 2014, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Whole-body diffusion-weighted imaging vs. FDG-PET for the detection of non-small-cell lung cancer. How do they measure up?

Wei Chen, Yun Lin, Dai-quan Zhou, 2010, Magnetic resonance imaging.

Is there a relationship between bone and critical illness?

Xiaolan Du, Lin Chen, Yao-zong Zhang, 2011, Medical hypotheses.

Iron-induced neuronal damage in a rat model of post-traumatic stress disorder

Wei Luo, Yangang Zhao, Jiqiang Zhang, 2016, Neuroscience.

Erythropoietin enhances mitochondrial biogenesis in cardiomyocytes exposed to chronic hypoxia through Akt/eNOS signalling pathway

Yingbin Xiao, Lin Chen, Shengkai Zhou, 2014, Cell biology international.

Pivotal role of activating transcription factor 6α in myocardial adaptation to chronic hypoxia.

Yingbin Xiao, Rui-yan Ma, Zhao Jian, 2012, The international journal of biochemistry & cell biology.

Regulation of ciliary function by fibroblast growth factor signaling identifies FGFR3-related disorders achondroplasia and thanatophoric dysplasia as ciliopathies

D. Krakow, G. Jansen, Ivan Duran, 2018, Human molecular genetics.

eNOS correlates with mitochondrial biogenesis in hearts of congenital heart disease with cyanosis.

Juan Xiao, Yingbin Xiao, Lin Chen, 2012, Arquivos brasileiros de cardiologia.

Deformed Skull Morphology Is Caused by the Combined Effects of the Maldevelopment of Calvarias, Cranial Base and Brain in FGFR2-P253R Mice Mimicking Human Apert Syndrome

Wei Xu, Xiaoqing Luo, F. Luo, 2017, International journal of biological sciences.

Gain-of-function mutation in FGFR3 in mice leads to decreased bone mass by affecting both osteoblastogenesis and osteoclastogenesis.

Di Chen, Yue Shen, H. Qi, 2010, Human molecular genetics.

A novel FGFR3-binding peptide inhibits FGFR3 signaling and reverses the lethal phenotype of mice mimicking human thanatophoric dysplasia.

C. Deng, Di Chen, P. Liu, 2012, Human molecular genetics.

Fibroblast Growth Factor Receptor 3 Deficiency Does Not Impair the Osteoanabolic Action of Parathyroid Hormone on Mice

C. Xian, F. Luo, Junlan Huang, 2016, International journal of biological sciences.

Reduces Bone Mass as in Human Apert Syndrome

Xiangjie Li, X. Wen, Lu-chuan Liu, 2013, American journal of medical genetics. Part A.

Fibroblast growth factor receptor 1 regulates the differentiation and activation of osteoclasts through Erk1/2 pathway.

Yue Shen, Qifen He, Xiumin Lu, 2009, Biochemical and biophysical research communications.

FGFR3 deficient mice have accelerated fracture repair

Wei Xu, F. Luo, Q. Tan, 2017, International journal of biological sciences.

Cross‐talk between FGF and other cytokine signalling pathways during endochondral bone development

M. Jin, Xiaolan Du, Lin Chen, 2012, Cell biology international.

Overexpression of H1 calponin in osteoblast lineage cells leads to a decrease in bone mass by disrupting osteoblast function and promoting osteoclast formation

Di Chen, Qifen He, Ying Zhu, 2013, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Inhibited Wnt Signaling Causes Age-Dependent Abnormalities in the Bone Matrix Mineralization in the Apert Syndrome FGFR2S252W/+ Mice

Lu-chuan Liu, Shichang Zhang, Li Zhang, 2015, PloS one.

Intermittent PTH (1-34) injection rescues the retarded skeletal development and postnatal lethality of mice mimicking human achondroplasia and thanatophoric dysplasia.

C. Deng, Junbao Yang, C. Xian, 2012, Human molecular genetics.

Exosomal transfer of osteoclast-derived miRNAs to chondrocytes contributes to osteoarthritis progression

Ge Zhang, Aiping Lu, Xiaohao Wu, 2021, Nature Aging.

Genetic inhibition of fibroblast growth factor receptor 1 in knee cartilage attenuates the degeneration of articular cartilage in adult mice.

Di Chen, Qian Chen, C. Deng, 2012, Arthritis and rheumatism.

Role of FGFs/FGFRs in skeletal development and bone regeneration

C. Xian, Yangli Xie, Xiaolan Du, 2012, Journal of cellular physiology.

The prediction of survival of patients with gastric cancer with PD-L1 expression using contrast-enhanced ultrasonography

Xi Wei, Qing Li, Lin Chen, 2016, Tumor Biology.

A Pro253Arg mutation in fibroblast growth factor receptor 2 (Fgfr2) causes skeleton malformation mimicking human Apert syndrome by affecting both chondrogenesis and osteogenesis.

Xiaoling Xu, Cuiling Li, L. Yin, 2008, Bone.

FGFR3 induces degradation of BMP type I receptor to regulate skeletal development.

C. Deng, Y. Mishina, Di Chen, 2014, Biochimica et biophysica acta.

Distribution and clinical features of Paragonimiasis skrjabini in Three Gorges Reservoir Region.

Li-fang Wang, Guang-xi Wang, Lin Chen, 2012, Parasitology international.

Adult antigens of Pagumogonimus skrjabini identified by the serum with paragonimiasis and analysis on their characterizations

Lin Chen, Xi-lin Zhang, J. Niu, 2010 .

Stereoscopic study on capillary density of early brain oedema in a dog postburn model.

Jian-sen Sun, D. Ying, Haitao Li, 2009, Injury.

Role of fibroblast growth factor receptor 1 in the bone development and skeletal diseases

Xiaolan Du, Lin Chen, Fu-bing Li, 2007 .

Increase of macrophage migration inhibitory factor (MIF) expression in cardiomyocytes during chronic hypoxia.

Q. Zhong, Yingbin Xiao, Zhao Jian, 2009, Clinica chimica acta; international journal of clinical chemistry.

The Association between Aortic Calcification and Fracture Risk in Postmenopausal Women in China: The Prospective Chongqing Osteoporosis Study

Jianzhong Xu, Huadong Zhou, Lin Chen, 2014, PloS one.

Identification of Differently Expressed Genes and Small Molecule Drugs for Tetralogy of Fallot by Bioinformatics Strategy

Qiang Gu, Yingbin Xiao, Xue-Tao Chen, 2014, Pediatric Cardiology.

Low Bone Mass is Associated with Stroke in Chinese Postmenopausal Women: The Chongqing Osteoporosis Study

Huadong Zhou, Dong Liu, Lin Chen, 2015, Cell Biochemistry and Biophysics.

A novel FGFR3-binding peptide inhibits FGFR3 signaling and reverses the lethal phenotype of mice mimicking human thanatophoric dysplasia.

C. Deng, Di Chen, C. Xian, 2012, Human molecular genetics.

Inactivation of Vhl in Osteochondral Progenitor Cells Causes High Bone Mass Phenotype and Protects Against Age‐Related Bone Loss in Adult Mice

Di Chen, Qifen He, F. Luo, 2014, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Genetic inhibition of fibroblast growth factor receptor 1 in knee cartilage attenuates the degeneration of articular cartilage in adult mice.

Di Chen, Qian Chen, C. Deng, 2012, Arthritis and rheumatism.

Localized all-cell knock-out (LACKO) strategy is needed for studying adult stage diseases

Ying Zhu, F. Luo, Xiaolan Du, 2012, Transgenic Research.