Changshun Shao

Author PubWeight™ 50.81‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Embryonic stem cells and somatic cells differ in mutation frequency and type. Proc Natl Acad Sci U S A 2002 2.17
2 Inflammatory cytokine-induced intercellular adhesion molecule-1 and vascular cell adhesion molecule-1 in mesenchymal stem cells are critical for immunosuppression. J Immunol 2010 2.12
3 CCR2-dependent recruitment of macrophages by tumor-educated mesenchymal stromal cells promotes tumor development and is mimicked by TNFα. Cell Stem Cell 2012 1.97
4 CUL4B activates Wnt/β-catenin signalling in hepatocellular carcinoma by repressing Wnt antagonists. J Pathol 2015 1.54
5 Mutation in CUL4B, which encodes a member of cullin-RING ubiquitin ligase complex, causes X-linked mental retardation. Am J Hum Genet 2007 1.41
6 MiR-182 overexpression in tumourigenesis of high-grade serous ovarian carcinoma. J Pathol 2012 1.38
7 Human DNA ligases I and III, but not ligase IV, are required for microhomology-mediated end joining of DNA double-strand breaks. Nucleic Acids Res 2008 1.37
8 HMGA2 overexpression-induced ovarian surface epithelial transformation is mediated through regulation of EMT genes. Cancer Res 2011 1.27
9 Brief report: interferon-gamma induces expansion of Lin(-)Sca-1(+)C-Kit(+) Cells. Stem Cells 2010 1.20
10 Modulation of DNA end joining by nuclear proteins. J Biol Chem 2005 1.14
11 miR-17-5p and miR-106a are involved in the balance between osteogenic and adipogenic differentiation of adipose-derived mesenchymal stem cells. Stem Cell Res 2012 1.14
12 Characterization of nuclear localization signal in the N terminus of CUL4B and its essential role in cyclin E degradation and cell cycle progression. J Biol Chem 2009 1.12
13 A missense mutation in SLC33A1, which encodes the acetyl-CoA transporter, causes autosomal-dominant spastic paraplegia (SPG42). Am J Hum Genet 2008 1.09
14 Resveratrol augments the canonical Wnt signaling pathway in promoting osteoblastic differentiation of multipotent mesenchymal cells. Exp Cell Res 2009 1.08
15 Berberine induces p53-dependent cell cycle arrest and apoptosis of human osteosarcoma cells by inflicting DNA damage. Mutat Res 2008 1.04
16 CRL4B catalyzes H2AK119 monoubiquitination and coordinates with PRC2 to promote tumorigenesis. Cancer Cell 2012 1.02
17 An osteopontin-integrin interaction plays a critical role in directing adipogenesis and osteogenesis by mesenchymal stem cells. Stem Cells 2014 1.00
18 Berberine, a genotoxic alkaloid, induces ATM-Chk1 mediated G2 arrest in prostate cancer cells. Mutat Res 2012 1.00
19 Somatic recombination redux. Nat Genet 2003 1.00
20 Lack of Cul4b, an E3 ubiquitin ligase component, leads to embryonic lethality and abnormal placental development. PLoS One 2012 1.00
21 Berberine radiosensitizes human esophageal cancer cells by downregulating homologous recombination repair protein RAD51. PLoS One 2011 0.97
22 53BP1 functions as a tumor suppressor in breast cancer via the inhibition of NF-κB through miR-146a. Carcinogenesis 2012 0.96
23 Metadherin enhances the invasiveness of breast cancer cells by inducing epithelial to mesenchymal transition. Cancer Sci 2011 0.96
24 Cullin 4B protein ubiquitin ligase targets peroxiredoxin III for degradation. J Biol Chem 2011 0.95
25 Chemokine receptor CXCR2 is transactivated by p53 and induces p38-mediated cellular senescence in response to DNA damage. Aging Cell 2013 0.93
26 MIF produced by bone marrow-derived macrophages contributes to teratoma progression after embryonic stem cell transplantation. Cancer Res 2012 0.93
27 Replication stress induces micronuclei comprising of aggregated DNA double-strand breaks. PLoS One 2011 0.93
28 Resveratrol modulates angiogenesis through the GSK3β/β-catenin/TCF-dependent pathway in human endothelial cells. Biochem Pharmacol 2010 0.92
29 Recurrence of the D100N mutation in a Chinese family with brachydactyly type A1: evidence for a mutational hot spot in the Indian hedgehog gene. Am J Med Genet A 2007 0.91
30 Mesenchymal stem/stromal cells induce the generation of novel IL-10-dependent regulatory dendritic cells by SOCS3 activation. J Immunol 2012 0.89
31 miR-106a represses the Rb tumor suppressor p130 to regulate cellular proliferation and differentiation in high-grade serous ovarian carcinoma. Mol Cancer Res 2013 0.87
32 Knockdown of Pnpla6 protein results in motor neuron defects in zebrafish. Dis Model Mech 2012 0.87
33 Serum withdrawal up-regulates human SIRT1 gene expression in a p53-dependent manner. J Cell Mol Med 2009 0.87
34 Radiation-induced genetic instability in vivo depends on p53 status. Mutat Res 2002 0.85
35 X-rays induce distinct patterns of somatic mutation in fetal versus adult hematopoietic cells. DNA Repair (Amst) 2007 0.84
36 Reduced apoptosis and increased deletion mutations at Aprt locus in vivo in mice exposed to repeated ionizing radiation. Cancer Res 2007 0.84
37 Prdx1 deficiency in mice promotes tissue specific loss of heterozygosity mediated by deficiency in DNA repair and increased oxidative stress. Mutat Res 2012 0.82
38 Neferine, an alkaloid ingredient in lotus seed embryo, inhibits proliferation of human osteosarcoma cells by promoting p38 MAPK-mediated p21 stabilization. Eur J Pharmacol 2011 0.82
39 X-linked intellectual disability gene CUL4B targets Jab1/CSN5 for degradation and regulates bone morphogenetic protein signaling. Biochim Biophys Acta 2013 0.80
40 Oxidative stress preferentially induces a subtype of micronuclei and mediates the genomic instability caused by p53 dysfunction. Mutat Res 2014 0.79
41 CUL4B promotes replication licensing by up-regulating the CDK2-CDC6 cascade. J Cell Biol 2013 0.79
42 Small scale genetic alterations contribute to increased mutability at the X-linked Hprt locus in vivo in Blm hypomorphic mice. DNA Repair (Amst) 2010 0.79
43 Whole-exome sequencing identifies a variant in TMEM132E causing autosomal-recessive nonsyndromic hearing loss DFNB99. Hum Mutat 2014 0.78
44 Identification and functional analysis of a SLC33A1: c.339T>G (p.Ser113Arg) variant in the original SPG42 family. Hum Mutat 2015 0.78
45 NANOG has a role in mesenchymal stem cells' immunomodulatory effect. Stem Cells Dev 2011 0.78
46 A novel deletion mutation in GJB1 causes X-linked Charcot-Marie-Tooth disease in a Han Chinese family. Muscle Nerve 2010 0.78
47 A human cell-based reporter detects microhomology-mediated end joining. Mutat Res 2011 0.78
48 Ionizing radiation is a potent inducer of mitotic recombination in mouse embryonic stem cells. Mutat Res 2011 0.77
49 Prenatal diagnosis of autosomal dominant hereditary spastic paraplegia (SPG42) caused by SLC33A1 mutation in a Chinese kindred. Prenat Diagn 2010 0.76
50 Role of the mismatch repair gene, Msh6, in suppressing genome instability and radiation-induced mutations. Mutat Res 2008 0.76
51 Differentiation of normal and leukemic cells by 2D light scattering label-free static cytometry. Opt Express 2016 0.75