Philip W. Tucker

Affiliations: 
1979-1980 Biochemistry The University of Mississippi Medical Center, Jackson, MS, United States 
 1980-1994 Microbiology University of Texas Southwestern Medical School, Dallas, TX, United States 
 1995- Cellular and Molecular Biology University of Texas at Austin, Austin, Texas, U.S.A. 
Area:
Molecular Biology, Oncology
Website:
https://www.bio.utexas.edu/research/tuckerlab/
Google:
"Philip William Tucker" OR "Philip W. Tucker" Texas""
Bio:

https://www.bio.utexas.edu/research/tuckerlab/class/TUCKERCV.htm
https://www.proquest.com/openview/3b70671c457a50301e7922bf737ad85e/1

Parents

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F. Albert Cotton grad student 1975 Texas A & M (Chemistry Tree)
 (Chemical and Crystallographic Studies of the Staphylococcal Nuclease)
Wendell August Landmann grad student 1975 Texas A & M (Chemistry Tree)
 (Co-Chairman)
Sidney Pestka post-doc 1974-1975 Roche Institute of Molecular Biology
Max F. Perutz post-doc 1975-1977 MRC-LMB (Chemistry Tree)
Frederick R. Blattner post-doc 1977-1979 UW Madison (Chemistry Tree)
Oliver Smithies post-doc 1977-1979 UW Madison (Neurotree)

Children

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Howard C. Crawford grad student 1994 UT Southwestern (Microtree)
Ching-Jung Huang grad student 2000 UT Austin
Li-Ping Sun grad student 2001 UT Austin
Grace E. Kubin grad student 2003 UT Austin
Dongkyoon Kim grad student 2004 UT Austin
John T. Powers grad student 2006 UT Austin
Baeck-Seung Lee grad student 2007 UT Austin
Josephine A. Curcio grad student 2008 UT Austin
Tara L. Rasmussen grad student 2008 UT Austin
BETA: Related publications

Publications

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Lee BS, Dekker JD, Lee BK, et al. (2017) Retraction for Lee et al., "The BCL11A Transcription Factor Directly Activates RAG Gene Expression and V(D)J Recombination". Molecular and Cellular Biology. 37
Lee BS, Dekker JD, Lee BK, et al. (2013) The BCL11A transcription factor directly activates RAG gene expression and V(D)J recombination. Molecular and Cellular Biology. 33: 1768-81
Fernandez I, Fridley KM, Arasappan D, et al. (2012) Gene expression profile and functionality of ESC-derived Lin-ckit+Sca-1+ cells are distinct from Lin-ckit+Sca-1+ cells isolated from fetal liver or bone marrow. Plos One. 7: e51944
Tidwell JA, Schmidt C, Heaton P, et al. (2011) Characterization of a new ARID family transcription factor (Brightlike/ARID3C) that co-activates Bright/ARID3A-mediated immunoglobulin gene transcription. Molecular Immunology. 49: 260-72
Foreman KW, Brown M, Park F, et al. (2011) Structural and functional profiling of the human histone methyltransferase SMYD3. Plos One. 6: e22290
Webb CF, Bryant J, Popowski M, et al. (2011) The ARID family transcription factor bright is required for both hematopoietic stem cell and B lineage development. Molecular and Cellular Biology. 31: 1041-53
Yao X, Nie H, Rojas IC, et al. (2010) The L2a element is a mouse CD8 silencer that interacts with MAR-binding proteins SATB1 and CDP. Molecular Immunology. 48: 153-63
Reddy ST, Ge X, Miklos AE, et al. (2010) Monoclonal antibodies isolated without screening by analyzing the variable-gene repertoire of plasma cells. Nature Biotechnology. 28: 965-9
An G, Miner CA, Nixon JC, et al. (2010) Loss of Bright/ARID3a function promotes developmental plasticity. Stem Cells (Dayton, Ohio). 28: 1560-7
Diehl F, Brown MA, van Amerongen MJ, et al. (2010) Cardiac deletion of Smyd2 is dispensable for mouse heart development. Plos One. 5: e9748
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