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Andre J. Van Wijnen
Researcher at University of Massachusetts Medical School
Publications - 239
Citations - 15151
Andre J. Van Wijnen is an academic researcher from University of Massachusetts Medical School. The author has contributed to research in topics: Transcription factor & Regulation of gene expression. The author has an hindex of 73, co-authored 239 publications receiving 14282 citations.
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Journal ArticleDOI
Runx2 (Cbfa1, AML-3) interacts with histone deacetylase 6 and represses the p21(CIP1/WAF1) promoter.
Jennifer J. Westendorf,S. Kaleem Zaidi,Jonathan E. Cascino,Rachel A. Kahler,Andre J. Van Wijnen,Jane B. Lian,Minoru Yoshida,Gary S. Stein,Xiaodong Li +8 more
TL;DR: Runx2 is identified as the first transcription factor to interact with HDAC6 and it is suggested thatHDAC6 may bind to Runx2 in differentiating osteoblasts to regulate tissue-specific gene expression.
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Dlx3 Transcriptional Regulation of Osteoblast Differentiation: Temporal Recruitment of Msx2, Dlx3, and Dlx5 Homeodomain Proteins to Chromatin of the Osteocalcin Gene
Mohammad Q. Hassan,Amjad Javed,Maria I. Morasso,Jeremy Karlin,Martin Montecino,Andre J. Van Wijnen,Gary S. Stein,Janet L. Stein,Jane B. Lian +8 more
TL;DR: It is proposed that multiple HD proteins in osteoblasts constitute a regulatory network that mediates development of the bone phenotype through the sequential association of distinct HD proteins with promoter regulatory elements.
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Identification of a nuclear matrix targeting signal in the leukemia and bone-related AML/CBF-alpha transcription factors
Congmei Zeng,Andre J. Van Wijnen,Janet L. Stein,Shari Meyers,Wuhua Sun,Lindsay S. Shopland,Jeanne B. Lawrence,Sheldon Penman,Jane B. Lian,Gary S. Stein,Scott W. Hiebert +10 more
TL;DR: The results suggest that the loss of the C-terminal domain of AML-1B is a frequent consequence of the leukemia-related t(8; 21) and t(3;21) translocations and may be functionally linked to the modified interrelationships between nuclear structure and gene expression characteristic of cancer cells.
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Transcriptional autoregulation of the bone related CBFA1/RUNX2 gene.
Hicham Drissi,Quyen Luc,A. Rauf Shakoori,Susana M. Chuva de Sousa Lopes,Je-Yong Choi,Anne Terry,Ming Hu,Stephen N. Jones,James C. Neil,Jane B. Lian,Janet L. Stein,Andre J. Van Wijnen,Gary S. Stein +12 more
TL;DR: Functional contributions of 5′ regulatory sequences conserved in rat, mouse and human CBFA1 genes to transcription are defined and indicate that the CB FA1 gene is autoregulated in part by negative feedback on its own promoter to stringently controlCBFA1 gene expression and function during bone formation.
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The Tissue-Specific Nuclear Matrix Protein, NMP-2, Is a Member of the AML/ CBF/PEBP2/Runt Domain Transcription Factor Family: Interactions with the Osteocalcin Gene Promoter
Harold L. Merriman,Andre J. Van Wijnen,Scott W. Hiebert,Joseph P. Bidwell,Edward G. Fey,Jane B. Lian,Janet L. Stein,Gary S. Stein +7 more
TL;DR: The results support the concept that the nuclear matrix mediates osteoblast-specific expression of the osteocalcin gene and indicate that AML family members may selectively partition between nuclear matrix and nonmatrix compartments.