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 1998 1998

Information analysis of human splice site mutations, Peter K. Rogan, Brian M. Faux, and Thomas D. Schneider

Submissions from 1997 1997

Klinefelter and trisomy X syndromes in patients with Prader-Willi syndrome and uniparental maternal disomy of chromosome 15--a coincidence?, M. G. Butler, L. K. Hedges, P. K. Rogan, J. R. Seip, S. B. Cassidy, and J. B. Moeschler

Report of the Third International Workshop on Human Chromosome 15 Mapping 1996. October 25-27, 1996 in Vancouver B.C., Canada., W. P. Robinson, B. Horsthemke, S. Leonard, S. Malcolm, C. Morton, R. D. Nicholls, R. J. Ritchie, P. Rogan, R. Schultz, S. Schwartz, J. Sharp, R. Trent, R. Wevrick, M. Williamson, and J. H. Knoll

Clinical spectrum and molecular diagnosis of Angelman and Prader-Willi syndrome patients with an imprinting mutation, Shinji Saitoh, Karin Buiting, Suzanne B. Cassidy, Jeffrey M. Conroy, Daniel J. Driscoll, James M. Gabriel, Gabriele Gillessen-Kaesbach, Christopher C. Glenn, Louise R. Greenswag, Bernhard Horsthemke, Ikuko Kondo, Katsuko Kuwajima, Norio Niikawa, Peter K. Rogan, Stuart Schwartz, James Seip, Charles A. Williams, and Robert D. Nicholls

Submissions from 1996 1996

Distinct 15q genotypes in Russell-Silver and ring 15 syndromes, Peter K. Rogan, James R. Seip, Daniel J. Driscoll, Peter R. Papenhausen, Virginia P. Johnson, Salmo Raskin, Amy L. Woodward, and Merlin G. Butler

Relationship of Sleep Abnormalities to Patient Genotypes in Prader-Willi Syndrome, Alexandros N. Vgontzas, Anthony Kales, James Seip, Maria J. Mascari, Edward O. Bixler, David C. Myers, Antonio Vela-Bueno, and Peter K. Rogan

Allele-specific replication of 15q11-q13 loci: A diagnostic test for detection of uniparental disomy, Lisa M. White, Peter K. Rogan, Robert D. Nicholls, Bai Lin Wu, Bruce Korf, and Joan H.M. Knoll

Submissions from 1994 1994

A new missense mutation, Arg719Gln, in the β-cardiac heavy chain myosin gene of patients with familial hypertrophic cardiomyopathy, Michael W. Consevage, Grant C. Salada, Barry G. Baylen, Roger L. Ladda, and Peter K. Rogan

A new missense mutation, Arg719Gln, in the β-cardiac heavy chain myosin gene of patients with familial hypertrophic cardiomyopathy, M. W. Consevage, G. C. Salada, B. G. Baylen, R. L. Ladda, and P. K. Rogan

Corrigendum: A new missense mutation, Arg719Gln, in the β-cardiac heavy chain myosin gene of patients with familial hypertrophic cardiomyopathy (Human Molecular Genetics (1994) 3 (1025-1026)), M. W. Consevage, G. C. Salada, B. G. Baylen, R. L. Ladda, and P. K. Rogan

Bloom syndrome and maternal uniparental disomy for chromosome 15, Trevor Woodage, Madhuri Prasad, Joanne W. Dixon, Roslyn E. Selby, Dennis R. Romain, Letizia M. Columbano-Green, David Graham, Peter K. Rogan, James R. Seip, Arabella Smith, and Ronald J. Trent

Submissions from 1992 1992

Introduction. Prader-Willi Syndrome Association Seventh Annual Scientific meeting, R. L. Ladda and P. K. Rogan

Pseudomosaicism trisomy 15 in amniocytes: Concern about the possibility of uniparental disomy in the fetus, M. J. Mascari, P. K. Rogan, L. S. Gannutz, M. P. McCurdy, C. D. Croft, T. R. Lichty, and R. L. Ladda

Mouse models for genomic imprinting and phenotypic features in Prader-Willi and Angelman syndromes, R. D. Nicholls, W. Gottlieb, K. M. Avidano, M. T.C. Jong, B. Horsthemke, L. B. Russell, S. J. Bultman, R. A. Spritz, P. K. Rogan, and E. M. Rinchik

Development of a molecular genetic data base for patients with Prader-Willi syndrome, P. K. Rogan, M. J. Mascari, R. D. Nicholls, and R. L. Ladda