Biochemistry Publications
Scientists in the Department of Biochemistry have expertise in genome dynamics, epigenetics, and gene expression; human genetics and clinical biochemistry; signal transduction and intracellular communication; macromolecular structure and dynamics; proteomics; and bioinformatics.
Visit the Department of Biochemistry Research website for additional information,
Submissions from 2005
A variant form of Oguchi disease mapped to 13q34 associated with partial deletion of GRK1 gene, Qingjiong Zhang, Fareeha Zulfiqar, S. Amer Riazuddin, Xueshan Xiao, Afshan Yasmeen, Peter K. Rogan, Raphael Caruso, Paul A. Sieving, Sheikh Riazuddin, and J. Fielding Hejtmancik
Submissions from 2004
Bipartite Pattern Discovery by Entropy Minimization-based Multiple Local Alignment, Chengpeng Bi and Peter K. Rogan
A Comprehensive Evaluation of Food Fortification with Folic Acid for the Primary Prevention of Neural Tube Defects, Shiliang Liu, Roy West, Edward Randell, Linda Longerich, Kathleen Steel O'Connor, Helen Scott, Marian Crowley, Angeline Lam, Victor Prabhakaran, and Catherine McCourt
High resolution detection of chromosome abnormalities with single copy Fluorescence In Situ Hybridization, Peter K. Rogan and Joan H.M. Knoll
Chemically Induced DNA Hypomethylation in Breast Carcinoma Cells Detected by the Amplification of Intermethylated Sites, Bekim Sadikovic, Thomas R. Haines, Darci T. Butcher, and David I. Rodenhiser
Enhanced Dupuytren's Disease Fibroblast Populated Collagen Lattice Contraction is Independent of Endogenous Active TGF-beta2, Raymond Tse, Jeffrey Howard, Yan Wu, and Bing Siang Gan
Development and Refinement of Pregnane X Receptor (PXR) DNA Binding Site Model Using Information Theory, Carrie A. Vyhlidal, Peter K. Rogan, and J. Steven Leeder
Submissions from 2003
Regulation of T-cell Activation by Phosphodiesterase 4B2 Requires its Dynamic Redistribution during Immunological Synapse Formation, Jacqueline Arp, Mark G. Kirchhof, Miren L. Baroja, Steven H. Nazarian, Thu A. Chau, Craig A. Strathdee, Eric H. Ball, and Joaquín Madrenas
Genomic Organization and Evolution of the CX3CR1/CCR8 Chemokine Receptor Locus, Mark E. DeVries, Henian Cao, Jian Wang, Luoling Xu, Alyson A. Kelvin, Longsi Ran, Luan A. Chau, Joaquin Madrenas, Robert A. Hegele, and David J. Kelvin
Genome-wide prediction, display and refinement of binding sites with information theory-based models, Sashidhar Gadiraju, Carrie A. Vyhlidal, J. Steven Leeder, and Peter K. Rogan
Genome-wide Prediction, Display and Refinement of Binding Sites with Information Theory-based Models, Sashidhar Gadiraju, Carrie A. Vyhlidal, J. Steven Leeder, and Peter K. Rogan
Elevated Levels of β-catenin and Fibronectin in Three-dimensional Collagen Cultures of Dupuytren's Disease Cells are Regulated by Tension in Vitro, Jeffrey C. Howard, Vincenzo M. Varallo, Douglas C. Ross, James H. Roth, Kenneth J. Faber, Benjamin Alman, and Bing Siang Gan
Submissions from 2002
Splice Variants But Not Mmutations of DNA Polymerase ß Are Common in Bladder Cancer, Tracy E. Thompson, Peter K. Rogan, John I. Risinger, and Jack A. Taylor
Splice variants but not mutations of DNA polymerase β are common in bladder cancer, Tracy E. Thompson, Jack A. Taylor, John I. Risinger, and Peter K. Rogan
Submissions from 2000
HDL-cholesterol-raising Effect of Orange Juice in Subjects with Hypercholesterolemia, Elzbieta M. Kurowska, J. David Spence, John Jordan, Stephen Wetmore, David J. Freeman, Leonard A. Piché, and Paula Serratore
Mosaicism in Prader-Willi syndrome., P. A. Mowery-Rushton, J. M. Hanchett, W. B. Zipf, P. K. Rogan, and U. Surti
Mosaicism in Prader-Willi syndrome [2] (multiple letters), R. D. Nicholls, P. A. Mowery-Rushton, J. M. Hanchett, W. B. Zipf, P. K. Rogan, and U. Surti
Redundant designations of BRCA1 intron 11 splicing mutation; c. 4216-2A>G; IVS11-2A>G; L78833, 37698, A>G, Stan R. Svojanovsky, Thomas D. Schneider, and Peter K. Rogan
Submissions from 1999
Chromosome breakage in the prader-Willi and Angelman syndromes involves recombination between large, transcribed repeats at proximal and distal breakpoints, James M. Amos-Landgraf, Ji Yonggang, Wayne Gottlieb, Theresa Depinet, Amy E. Wandstrat, Suzanne B. Cassidy, Daniel J. Driscoll, Peter K. Rogan, Stuart Schwartz, and Robert D. Nicholls
Maternal uniparental disomy of chromosome 14 confined to an interstitial segment (14q23-14q24.2), Rick A. Martin, Darrin W. Sabol, and Peter K. Rogan
Imprinting-mutation mechanisms in Prader-Willi syndrome, T. Ohta, T. A. Gray, P. K. Rogan, K. Buiting, J. M. Gabriel, S. Saitoh, B. Muralidhar, B. Bilienska, M. Krajewska-Walasek, D. J. Driscoll, B. Horsthemke, M. G. Butler, and Robert D. Nicholls
Maternal uniparental disomy of chromosome 21 in a normal child, Peter K. Rogan, Darrin W. Sabol, and Hope H. Punnett
Erratum: Information analysis of human splice site mutations (Human Mutation (1998) 12 (153-171)), P. K. Rogan, B. M. Faux, and T. D. Schneider
Submissions from 1998
Organization of the ABCR gene: Analysis of promoter and splice junction sequences, Rando Allikmets, Wyeth W. Wasserman, Amy Hutchinson, Philip Smallwood, Jeremy Nathans, Peter K. Rogan, Thomas D. Schneider, and Michael Dean
Autosomal dominant zonular cataract with sutural opacities is associated with a splice mutation in the betaA3/A1-crystallin gene., C. Kannabiran, P. K. Rogan, L. Olmos, S. Basti, G. N. Rao, M. Kaiser-Kupfer, and J. F. Hejtmancik