Dan E Wells
Dan E Wells
Professor Biology and Biochemistry, University of Houston
Verified email at uh.edu
TitleCited byYear
The genome of the Western clawed frog Xenopus tropicalis
U Hellsten, RM Harland, MJ Gilchrist, D Hendrix, J Jurka, V Kapitonov, ...
Science 328 (5978), 633-636, 2010
5912010
Cloning of the putative tumour suppressor gene for hereditary multiple exostoses (EXT1)
J Ahn, HJ Lüdecke, S Lindow, WA Horton, B Lee, MJ Wagner, ...
Nature genetics 11 (2), 137, 1995
4431995
Disruption of gastrulation and heparan sulfate biosynthesis in EXT1-deficient mice
X Lin, G Wei, Z Shi, L Dryer, JD Esko, DE Wells, MM Matzuk
Developmental biology 224 (2), 299-311, 2000
4132000
Genetic heterogeneity in families with hereditary multiple exostoses
A Cook, W Raskind, SH Blanton, RM Pauli, RG Gregg, CA Francomano, ...
American journal of human genetics 53 (1), 71, 1993
2221993
Loss of chromosome arm 8p loci in prostate cancer: mapping by quantitative allelic imbalance
D MacGrogan, A Levy, D Bostwick, M Wagner, D Wells, R Bookstein
Genes, Chromosomes and Cancer 10 (3), 151-159, 1994
2091994
Structure of a human histone cDNA: evidence that basally expressed histone genes have intervening sequences and encode polyadenylylated mRNAs
D Wells, L Kedes
Proceedings of the National Academy of Sciences 82 (9), 2834-2838, 1985
1851985
A comprehensive compilation and alignment of histones and histone genes
D Wells, C McBride
Nucleic acids research 17 (Suppl), r311, 1989
1611989
Compilation analysis of histones and histone genes
DE Wells
Nucleic acids research 14 (Suppl), r119, 1986
1481986
Hereditary multiple exostoses (EXT): mutational studies of familial EXT1 cases and EXT-associated malignancies.
JT Hecht, D Hogue, Y Wang, SH Blanton, M Wagner, LC Strong, ...
American journal of human genetics 60 (1), 80, 1997
1381997
Molecular dissection of a contiguous gene syndrome: localization of the genes involved in the Langer—Giedion syndrome
HJ Lüdecke, M J. Wagner, J Nardmann, BL Pillo, J E. Parrish, P J. Willems, ...
Human molecular genetics 4 (1), 31-36, 1995
1321995
Mutation screening of the EXT1 and EXT2 genes in patients with hereditary multiple exostoses
C Philippe, DE Porter, ME Emerton, DE Wells, A Hamish, RW Simpson, ...
The American Journal of Human Genetics 61 (3), 520-528, 1997
1241997
Light induction of a vertebrate clock gene involves signaling through blue-light receptors and MAP kinases
N Cermakian, MP Pando, CL Thompson, AB Pinchak, CP Selby, ...
Current Biology 12 (10), 844-848, 2002
1192002
Chromosomal localization of the human and mouse hyaluronan synthase genes
AP Spicer, MF Seldin, AS Olsen, N Brown, DE Wells, NA Doggett, N Itano, ...
Genomics 41 (3), 493-497, 1997
1161997
Accumulation in embryogenesis of five mRNAs enriched in the ectoderm of the sea urchin pluteus
AM Bruskin, AL Tyner, DE Wells, RM Showman, WH Klein
Developmental biology 87 (2), 308-318, 1981
1071981
Mutation in CEP290 discovered for cat model of human retinal degeneration
M Menotti-Raymond, VA David, AA Schäffer, R Stephens, D Wells, ...
Journal of Heredity 98 (3), 211-220, 2007
982007
A hybrid cell mapping panel for regional localization of probes to human chromosome 8
MJ Wagner, Y Ge, M Siciliano, DE Wells
Genomics 10 (1), 114-125, 1991
891991
Identification of intrinsic termination sites in vitro for RNA polymerase II within eukaryotic gene sequences
D Reines, D Wells, MJ Chamberlin, CM Kane
Journal of molecular biology 196 (2), 299-312, 1987
861987
Unusual structure, evolutionary conservation of non-coding sequences and numerous pseudogenes characterize the human H3. 3 histone multigene family
D Wells, D Hoffman, L Kedes
Nucleic acids research 15 (7), 2871-2889, 1987
811987
Molecular definition of the shortest region of deletion overlap in the Langer-Giedion syndrome
HJ Lüdecke, C Johnson, MJ Wagner, DE Wells, C Turleau, N Tommerup, ...
American journal of human genetics 49 (6), 1197, 1991
781991
Evaluation of locus heterogeneity and EXT1 mutations in 34 families with hereditary multiple exostoses
WH Raskind, EU Conrad III, M Matsushita, EM Wijsman, DE Wells, ...
Human mutation 11 (3), 231-239, 1998
731998
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