Yang Luo

发表

Biallelic Mutations in CFAP43 and CFAP44 Cause Male Infertility with Multiple Morphological Abnormalities of the Sperm Flagella.

F. Zhang, Jian Wang, Hongyan Wang, 2017, American journal of human genetics.

Novel and recurrent mutations in the EXT1 and EXT2 genes in Chinese kindreds with multiple osteochondromas

Yang Luo, Yuhong Wu, X. Xing, 2013, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.

Identification of a mutation in the WISP3 gene in three unrelated families with progressive pseudorheumatoid dysplasia.

Yang Luo, X. Xing, Hong-wei Ma, 2015, Molecular medicine reports.

Overexpression of DOC-1R Inhibits Cell Cycle G1/S Transition by Repressing CDK2 Expression and Activation

Yang Luo, Shu-sen Wang, Jinlan Gao, 2013, International journal of biological sciences.

Novel vitamin D 1α-hydroxylase gene mutations in a Chinese vitamin-D-dependent rickets type I patient

Yang Luo, Jian Ma, Hong-wei Ma, 2011, Journal of Genetics.

To control or to be controlled? Dual roles of CDK2 in DNA damage and DNA damage response.

Yingying Guo, Yang Luo, X. Xing, 2019, DNA repair.

Five novel mutations in the ADAR1 gene associated with dyschromatosis symmetrica hereditaria

Zhen Wang, Yang Luo, Yuhong Wu, 2014, BMC Medical Genetics.

Knock-in human GDF5 proregion L373R mutation as a mouse model for proximal symphalangism

Heyi Wang, Yang Luo, X. Xing, 2017, Oncotarget.

Cyclin G2 Is Involved in the Proliferation of Placental Trophoblast Cells and Their Interactions with Endothelial Cells

Yang Luo, T. Meng, Hai-ying Chen, 2020, Medical science monitor : international medical journal of experimental and clinical research.

Mutation analysis of the negative regulator cyclin G2 in gastric cancer

Yang Luo, Shu-sen Wang, Jinlan Gao, 2011 .

Molecular Genetic Characterization of a Chinese Family with Severe Split Hand/Foot Malformation.

C. Chen, Xue Zhang, Yang Luo, 2017, Genetic testing and molecular biomarkers.

Cyclin G2 regulates canonical Wnt signalling via interaction with Dapper1 to attenuate tubulointerstitial fibrosis in diabetic nephropathy

Yang Luo, X. Xing, Shu-sen Wang, 2020, Journal of cellular and molecular medicine.

A missense mutation of HOXA13 underlies hand-foot-genital syndrome in a Chinese family

C. Chen, Xue Zhang, Yang Luo, 2017, Journal of Genetics.

A splice donor site mutation in HOXD13 underlies synpolydactyly with cortical bone thinning.

Yang Luo, Yuhong Wu, Yuyang Shang, 2013, Gene.

A Novel Splicing Mutation Identified in a Chinese Family with X-linked Alport Syndrome Using Targeted Next-Generation Sequencing.

C. Chen, Xue Zhang, Yang Luo, 2016, Genetic testing and molecular biomarkers.

Novel point mutations in GDF5 associated with two distinct limb malformations in Chinese: brachydactyly type C and proximal symphalangism

Li Jiang, Miao Sun, W. H. Lo, 2008, Journal of Human Genetics.

Mutations in mevalonate pathway genes in patients with familial or sporadic porokeratosis

Yang Luo, Lihua Cao, Shu-sen Wang, 2018, The Journal of dermatology.

Screening of Duchenne Muscular Dystrophy (DMD) Mutations and Investigating Its Mutational Mechanism in Chinese Patients

Xue Zhang, Feng Zhang, Yang Luo, 2014, PloS one.

Cyclin G2 upregulation impairs migration, invasion, and network formation through RNF123/Dvl2/JNK signaling in the trophoblast cell line HTR8/SVneo, a possible role in preeclampsia

Yang Luo, T. Meng, Hai-ying Chen, 2020, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Cyclin G2 reverses immunosuppressive tumor microenvironment and potentiates PD-1 blockade in glioma

Yang Luo, X. Xing, Shu-sen Wang, 2021, Journal of experimental & clinical cancer research : CR.

Rare variants in FANCA induce premature ovarian insufficiency

L. Jin, Qinghua Shi, Feng Zhang, 2019, Human Genetics.

Cyclin G2 in macrophages triggers CTL-mediated antitumor immunity and antiangiogenesis via interferon-gamma

Yang Luo, X. Xing, Shu-sen Wang, 2022, Journal of experimental & clinical cancer research : CR.

Efficient CNV breakpoint analysis reveals unexpected structural complexity and correlation of dosage‐sensitive genes with clinical severity in genomic disorders

J. Lupski, C. Carvalho, Hongyan Wang, 2017, Human molecular genetics.

Cyclin G2 suppresses Wnt/β-catenin signaling and inhibits gastric cancer cell growth and migration through Dapper1

Chunhua Yang, Yang Luo, Sen Li, 2018, Journal of experimental & clinical cancer research : CR.

Cyclin G2 suppresses Wnt/β-catenin signaling and inhibits gastric cancer cell growth and migration through Dapper1

Chunhua Yang, Yang Luo, X. Xing, 2018, Journal of Experimental & Clinical Cancer Research.

Copy-number mutations on chromosome 17q24.2-q24.3 in congenital generalized hypertrichosis terminalis with or without gingival hyperplasia.

Miao Sun, Xin Li, Lin He, 2009, American journal of human genetics.

Cyclin G2 Inhibits the Warburg Effect and Tumour Progression by Suppressing LDHA Phosphorylation in Glioma

Yang Luo, X. Xing, Sen Li, 2019, International journal of biological sciences.

A novel mutation in the EXT1 gene identified in a Han Chinese kindred with hereditary multiple exostosis.

Yang Luo, Lihua Cao, Shu-sen Wang, 2010, Genetic testing and molecular biomarkers.

Cyclin G2 Suppresses Estrogen-Mediated Osteogenesis through Inhibition of Wnt/β-Catenin Signaling

Yang Luo, Shu-sen Wang, Jinlan Gao, 2014, PloS one.

Cyclin G2 promotes the formation of smooth muscle cells derived foam cells in atherosclerosis via PP2A/NF-κB/LOX-1 pathway

Yang Luo, X. Xing, Shu-sen Wang, 2021, Annals of translational medicine.

Mutations of the EPHA2 receptor tyrosine kinase gene cause autosomal dominant congenital cataract

D. Mackey, S. Bhattacharya, J. Craig, 2009, Human mutation.

Three novel mutations of APC gene in Chinese patients with familial adenomatous polyposis

Yang Luo, Hong-wei Ma, Sen Li, 2016, Tumor Biology.

Cyclin G2 Suppresses Glomerulosclerosis by Regulating Canonical Wnt Signalling

Yang Luo, X. Xing, Shu-sen Wang, 2018, BioMed research international.

Clinical and genetic characteristics of Chinese patients with familial or sporadic pediatric cataract

Xue Zhang, Yang Luo, Lihua Cao, 2018, Orphanet Journal of Rare Diseases.

Cyclin G2 Inhibits Oral Squamous Cell Carcinoma Growth and Metastasis by Binding to IGFBP3 and Regulating the FAK-SRC-STAT Signaling Pathway

Yang Luo, Sen Li, Di Zhang, 2020, Frontiers in Oncology.

Cyclin G2 Inhibits Oral Squamous Cell Carcinoma Growth and Metastasis by Binding to IGFBP3 and Regulating the FAK-SRC-STAT Signaling Pathway

Yang Luo, Sen Li, Di Zhang, 2020, bioRxiv.

Mutation analysis of a Chinese pedigree with triphalangeal thumb-polysyndactyly syndrome.

Yang Luo, X. Xing, Shu-sen Wang, 2014, Genetics and molecular research : GMR.