Wanguo Liu

发表

Mutations in AXIN2 cause colorectal cancer with defective mismatch repair by activating β-catenin/TCF signalling

David I. Smith, Xiangyang Dong, S. Thibodeau, 2000, Nature Genetics.

Mutations in components of the Wnt signaling pathway in gastric cancer.

K. Pan, Lian Zhang, W. You, 2008, World journal of gastroenterology.

p53 Inactivation Upregulates p73 Expression through E2F-1 Mediated Transcription

T. Sakai, A. Thor, S. Anant, 2012, PloS one.

Identification and Chromosomal Localization of CTNNAL1, a Novel Protein Homologous to α-Catenin

David I. Smith, R. Urrutia, V. Shridhar, 1998 .

PTEN/MMAC1 mutations identified in small cell, but not in non-small cell lung cancers

David I. Smith, D. Tindall, W. Franklin, 1998, Oncogene.

Epigenetic silencing of TCEAL7 (Bex4) in ovarian cancer

David I. Smith, L. Hartmann, J. Chien, 2005, Oncogene.

The pathogenicity of the Pro1148Ala substitution in the FBN1 gene: causing or predisposing to Marfan syndrome and aortic aneurysm, or clinically innocent?

U. Francke, I. Schrijver, Wanguo Liu, 1997, Human Genetics.

p53 Mutations in Barrett's esophagus predict poor response to photodynamic therapy

Kenneth K Wang, N. Buttar, T. Sebo, 2001 .

FHIT and TSG101 in thyroid tumours: aberrant transcripts reflect rare abnormal RNA processing events of uncertain pathogenetic or clinical significance

N. Eberhardt, I. Hay, J. Goellner, 2000, Clinical endocrinology.

The gene for microfibril-associated protein-1 (MFAP1) is located several megabases centromeric to FBN1 and is not mutated in Marfan syndrome

U. Francke, J. Faraco, Wanguo Liu, 1997, Human Genetics.

Identification and Characterization of Putative Tumor Suppressor NGB, a GTP-Binding Protein That Interacts with the Neurofibromatosis 2 Protein

D. Coppola, S. Nicosia, J. Cheng, 2007, Molecular and Cellular Biology.

Acetylation of androgen receptor by ARD1 promotes dissociation from HSP90 complex and prostate tumorigenesis

Zehua Wang, Haitao Zhang, Wanguo Liu, 2016, Oncotarget.

Loss of imprinting and allele switching of p73 in renal cell carcinoma

David I. Smith, D. Tindall, D. Bostwick, 1998, Oncogene.

A Molecular Cytogenetic Analysis of 7 q 31 in Prostate Cancer 1

David I. Smith, D. Bostwick, Haojie Huang, 2006 .

Human acid ceramidase is overexpressed but not mutated in prostate cancer

D. Bostwick, W. Liu, A. Yokomizo, 2000, Genes, chromosomes & cancer.

Luteinizing hormone β polymorphism and risk of familial and sporadic prostate cancer

S. Thibodeau, S. McDonnell, J. Cunningham, 2003 .

Loss of expression of the DRR 1 gene at chromosomal segment 3p21.1 in renal cell carcinoma

D. Bostwick, B. Opalka, J. Qian, 2000, Genes, chromosomes & cancer.

The Cloning of Tumor Suppressor Genes from the Short Arm of Human Chromosome 3 that Play a Role in the Development of Renal Cell Carcinoma

David I. Smith, V. Shridhar, Wanguo Liu, 1995 .

Centrosome amplification drives chromosomal instability in breast tumor development

Carol Reynolds, C. Reynolds, W. Lingle, 2002, Proceedings of the National Academy of Sciences of the United States of America.

Mutational spectrum of β-catenin, AXIN1, and AXIN2 in hepatocellular carcinomas and hepatoblastomas

David I. Smith, Xiangyang Dong, D. Nagorney, 2002, Oncogene.

Identification of speckle-type POZ protein somatic mutations in African American prostate cancer

E. Buckles, Wanguo Liu, C. Qian, 2014, Asian journal of andrology.

Inactivation of androgen-induced regulator ARD1 inhibits androgen receptor acetylation and prostate tumorigenesis

J. Bavarva, Yingchun Li, Wanguo Liu, 2012, Proceedings of the National Academy of Sciences.

β-catenin inhibitor ICAT modulates the invasive motility of melanoma cells.

L. Papon, B. Job, F. Rambow, 2014, Cancer research.

Mutations in CHEK2 associated with prostate cancer risk.

David I. Smith, J. Cheville, D. Tindall, 2003, American journal of human genetics.

Silent mutation induces exon skipping of fibrillin-1 gene in Marfan syndrome

U. Francke, Wanguo Liu, C. Qian, 1997, Nature Genetics.

Characterization of CHEK2 mutations in prostate cancer

Junjie Chen, Wanguo Liu, Xiang-yang Dong, 2006, Human mutation.

Truncating variants in p53AIP1 disrupting DNA damage-induced apoptosis are associated with prostate cancer risk.

D. Tindall, D. Schaid, F. Couch, 2006, Cancer research.

Mutation and expression analysis of the p73 gene in prostate cancer

D. Tindall, D. Bostwick, Liang Cheng, 1999, The Prostate.

Overexpression of the wild type p73 gene in human bladder cancer

D. Tindall, D. Bostwick, Liang Cheng, 1999, Oncogene.

Polymorphisms in the promoter region of the neutrophil elastase gene are associated with lung cancer development.

Claude Deschamps, James Jett, J. Jett, 2002, Clinical cancer research : an official journal of the American Association for Cancer Research.

Role for the p53 homologue p73 in E2F-1-induced apoptosis

David I. Smith, K. Tsai, T. Jacks, 2000, Nature.

KIF3a Promotes Proliferation and Invasion via Wnt Signaling in Advanced Prostate Cancer

Yingchun Li, Wanguo Liu, C. Qian, 2014, Molecular Cancer Research.

Cell Cycle and Senescence KIF 3 a Promotes Proliferation and Invasion via Wnt Signaling in Advanced Prostate Cancer

Zehua Wang, Yingchun Li, Wanguo Liu, 2014 .

Genome-Wide Transcriptional Profiling Reveals MicroRNA-Correlated Genes and Biological Processes in Human Lymphoblastoid Cell Lines

Hugues Sicotte, Shannon K. McDonnell, Yan W. Asmann, 2009, PloS one.

The Human p 73 Promoter : Characterization and Identification of Functional E 2 F Binding Sites 1

P. V. Stoop, W. Kaelin, M. Irwin, 2014 .

The human p73 promoter: characterization and identification of functional E2F binding sites.

W. Kaelin, P. V. D. van der Stoop, M. Irwin, 2002, Neoplasia.

Mutations in the Human naked cuticle Homolog NKD1 Found in Colorectal Cancer Alter Wnt/Dvl/β-Catenin Signaling

Jianhui Guo, Stephen N. Thibodeau, Richard Hamelin, 2009, PloS one.

Unique substitution of CHEK2 and TP53 mutations implicated in primary prostate tumors and cancer cell lines

J. Cheville, D. Tindall, R. Neumann, 2006, Human mutation.

Mutational analysis of thirty-two double-strand DNA break repair genes in breast and pancreatic cancers.

J. Cerhan, F. Couch, S. Thibodeau, 2008, Cancer research.

FAVL elevation in human tumors disrupts Fanconi anemia pathway signaling and promotes genomic instability and tumor growth.

D. Tindall, Hong Wang, M. McNiven, 2010, The Journal of clinical investigation.

Premature termination mutations in FBN1: distinct effects on differential allelic expression and on protein and clinical phenotypes.

Uta Francke, Peter Oefner, Iris Schrijver, 2002, American journal of human genetics.

Marfan Database (third edition): new mutations and new routines for the software

Hanns-Georg Klein, Christophe Béroud, Gwenaëlle Collod-Béroud, 1998, Nucleic Acids Res..

Multi-exon deletions of the FBN1 gene in Marfan syndrome

U. Francke, I. Schrijver, T. Brenn, 2001, BMC Medical Genetics.

Gluthatione-S-transferase P1 polymorphism I105V in familial and sporadic prostate cancer.

D. Tindall, D. Schaid, S. Thibodeau, 2004, Cancer genetics and cytogenetics.

Detection of frameshift mutations of RIZ in gastric cancers with microsatellite instability.

K. Pan, Lian Zhang, W. You, 2004, World journal of gastroenterology.

Genetic determinants of lung cancer short-term survival: the role of glutathione-related genes.

T. Lesnick, J. Jett, J. Sloan, 2002, Lung cancer.

High throughput detection of microsatellite instability by denaturing high‐performance liquid chromatography

S. Thibodeau, K. Pan, Lian Zhang, 2003, Human mutation.

ARD1/NAA10 acetylation in prostate cancer

Katherine J. Kuhns, Wanguo Liu, Guanyi Zhang, 2018, Experimental & Molecular Medicine.

Cloning and functional analysis of human mTERFL encoding a novel mitochondrial transcription termination factor-like protein.

Min Yu, Wei Tang, Wanguo Liu, 2005, Biochemical and biophysical research communications.

DIXDC1 isoform, l-DIXDC1, is a novel filamentous actin-binding protein.

Xianshu Wang, J. Chien, Lin Chen, 2006, Biochemical and biophysical research communications.

Frequent truncating mutation of TFAM induces mitochondrial DNA depletion and apoptotic resistance in microsatellite-unstable colorectal cancer.

Dongchon Kang, Jianhui Guo, S. Thibodeau, 2011, Cancer research.

ARD1/NAA10 acetylation in prostate cancer

Katherine J. Kuhns, Zehua Wang, Wanguo Liu, 2018, Experimental & Molecular Medicine.

Clinical and Functional Analyses of p73R1 Mutations in Prostate Cancer

Wanguo Liu, 2005 .

Abstract 4937: KIF3A promotes prostate cancer cell proliferation, migration, and invasion via activation of Dvl2 and the Wnt signaling pathway.

Yingchun Li, Wanguo Liu, C. Qian, 2013 .

HEF1, a novel target of Wnt signaling, promotes colonic cell migration and cancer progression

Jasmin H. Bavarva, S. Thibodeau, J. Bavarva, 2011, Oncogene.

Denaturing high performance liquid chromatography (DHPLC) used in the detection of germline and somatic mutations.

S N Thibodeau, C. James, S. Thibodeau, 1998, Nucleic acids research.

Cysteine substitutions in epidermal growth factor-like domains of fibrillin-1: distinct effects on biochemical and clinical phenotypes.

U. Francke, I. Schrijver, T. Brenn, 1999, American journal of human genetics.

PTEN/MMAC1 mutations and EGFR amplification in glioblastomas.

C. James, W. Liu, B. Alderete, 1997, Cancer research.

Cloning of the human homolog of conductin (AXIN2), a gene mapping to chromosome 17q23-q24.

W. Liu, A. Yokomizo, D. Smith, 1999, Genomics.

Genomic organization and mutation analysis of p73 in oligodendrogliomas with chromosome 1 p-arm deletions.

W. Liu, H. Huang, D. Smith, 1998, Genomics.

Activation of p73 silent allele in lung cancer.

D. Tindall, W. Liu, A. Yokomizo, 1998, Cancer research.

p73 mutations are not detected in sporadic and hereditary breast cancer

David I. Smith, F. Couch, N. Lindor, 1999, Breast Cancer Research and Treatment.

Differential expression and allelotyping of the p73 gene in neuroblastoma.

D. Tindall, S. Thibodeau, W. Liu, 2000, International journal of oncology.

Mutant fibrillin-1 monomers lacking EGF-like domains disrupt microfibril assembly and cause severe marfan syndrome.

U. Francke, T. Brenn, H. Furthmayr, 1996, Human molecular genetics.

Exon skipping in IVD RNA processing in isovaleric acidemia caused by point mutations in the coding region of the IVD gene.

J. Vockley, W. Liu, P. Rogan, 2000, American journal of human genetics.

Denaturing HPLC-identified novel FBN1 mutations, polymorphisms, and sequence variants in Marfan syndrome and related connective tissue disorders.

P. Oefner, U. Francke, Wanguo Liu, 1997, Genetic testing.

A Gly1127Ser mutation in an EGF-like domain of the fibrillin-1 gene is a risk factor for ascending aortic aneurysm and dissection.

U. Francke, D. Miller, T. Aoyama, 1995, American journal of human genetics.

FAVL elevation in human tumors disrupts Fanconi anemia pathway signaling and promotes genomic instability and tumor growth.

D. Tindall, Hong Wang, M. McNiven, 2010, The Journal of clinical investigation.