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Publications

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1988
Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification., Chamberlain, J. S., Gibbs R. A., Ranier J. E., Nguyen P. N., and Caskey C. T. , Nucleic acids research, 1988 Dec 9, Volume 16, Issue 23, p.11141-56, (1988) Abstract
1989
Automated DNA sequencing methods for detection and analysis of mutations: applications to the Lesch-Nyhan syndrome., Edwards, A., Gibbs R. A., Nguyen P. N., Ansorge W., and Caskey C. T. , Transactions of the Association of American Physicians, 1989, Volume 102, p.185-94, (1989)
Detection of single DNA base differences by competitive oligonucleotide priming., Gibbs, R. A., Nguyen P. N., and Caskey C. T. , Nucleic acids research, 1989 Apr 11, Volume 17, Issue 7, p.2437-48, (1989) Abstract
Identification of mutations leading to the Lesch-Nyhan syndrome by automated direct DNA sequencing of in vitro amplified cDNA., Gibbs, R. A., Nguyen P. N., McBride L. J., Koepf S. M., and Caskey C. T. , Proceedings of the National Academy of Sciences of the United States of America, 1989 Mar, Volume 86, Issue 6, p.1919-23, (1989) Abstract
1990
Long HIV-1 incubation periods and dynamics of transmission within a family., Burger, H., Belman A. L., Grimson R., Kaell A., Flaherty K., Gulla J., Gibbs R. A., Nguyun P. N., and Weiser B. , Lancet, 1990 Jul 21, Volume 336, Issue 8708, p.134-6, (1990) Abstract
Multiplex DNA deletion detection and exon sequencing of the hypoxanthine phosphoribosyltransferase gene in Lesch-Nyhan families., Gibbs, R. A., Nguyen P. N., Edwards A., Civitello A. B., and Caskey C. T. , Genomics, 1990 Jun, Volume 7, Issue 2, p.235-44, (1990) Abstract
1991
Evolution of human immunodeficiency virus type 1 nucleotide sequence diversity among close contacts., Burger, H., Weiser B., Flaherty K., Gulla J., Nguyen P. N., and Gibbs R. A. , Proceedings of the National Academy of Sciences of the United States of America, 1991 Dec 15, Volume 88, Issue 24, p.11236-40, (1991) Abstract
Alu-primed polymerase chain reaction for regional assignment of 110 yeast artificial chromosome clones from the human X chromosome: identification of clones associated with a disease locus., Nelson, D. L., Ballabio A., Victoria M. F., Pieretti M., Bies R. D., Gibbs R. A., Maley J. A., Chinault A. C., Webster T. D., and Caskey C. T. , Proceedings of the National Academy of Sciences of the United States of America, 1991 Jul 15, Volume 88, Issue 14, p.6157-61, (1991) Abstract
1993
Fine structure of the human FMR1 gene., Eichler, E. E., Richards S., Gibbs R. A., and Nelson D. L. , Human molecular genetics, 1993 Aug, Volume 2, Issue 8, p.1147-53, (1993) Abstract
1994
Molecular cloning of the wild-type and mutant thyA gene from Shigella flexneri Y., Nur-E-Kamal, M. S., Al Mamun A. A., and Ahmed Z. U. , Microbiology and immunology, 1994, Volume 38, Issue 4, p.309-12, (1994) Abstract
Fine structure of the human FMR1 gene., Eichler, E. E., Richards S., Gibbs R. A., and Nelson D. L. , Human molecular genetics, 1994 Apr, Volume 3, Issue 4, p.684-5, (1994)
1995
130 kb of DNA sequence reveals two new genes and a regional duplication distal to the human iduronate-2-sulfate sulfatase locus., Timms, K. M., Lu F., Shen Y., Pierson C. A., Muzny D. M., Gu Y., Nelson D. L., and Gibbs R. A. , Genome research, 1995 Aug, Volume 5, Issue 1, p.71-8, (1995) Abstract
1996
Duplication of a gene-rich cluster between 16p11.1 and Xq28: a novel pericentromeric-directed mechanism for paralogous genome evolution., Eichler, E. E., Lu F., Shen Y., Antonacci R., Jurecic V., Doggett N. A., Moyzis R. K., Baldini A., Gibbs R. A., and Nelson D. L. , Human molecular genetics, 1996 Jul, Volume 5, Issue 7, p.899-912, (1996) Abstract
Identification of FMR2, a novel gene associated with the FRAXE CCG repeat and CpG island., Gu, Y., Shen Y., Gibbs R. A., and Nelson D. L. , Nature genetics, 1996 May, Volume 13, Issue 1, p.109-13, (1996) Abstract
1997
Sequencing and functional analysis of the SNRPN promoter: in vitro methylation abolishes promoter activity., Huq, A. H., Sutcliffe J. S., Nakao M., Shen Y., Gibbs R. A., and Beaudet A. L. , Genome research, 1997 Jun, Volume 7, Issue 6, p.642-8, (1997) Abstract
Molecular and phenotypic variation in patients with severe Hunter syndrome., Timms, K. M., Bondeson M. L., Ansari-Lari M. A., Lagerstedt K., Muzny D. M., Dugan-Rocha S. P., Nelson D. L., Pettersson U., and Gibbs R. A. , Human molecular genetics, 1997 Mar, Volume 6, Issue 3, p.479-86, (1997) Abstract
1999
Identification of three novel Ca(2+) channel gamma subunit genes reveals molecular diversification by tandem and chromosome duplication., Burgess, D. L., Davis Caleb F., Gefrides L. A., and Noebels J. L. , Genome research, 1999 Dec, Volume 9, Issue 12, p.1204-13, (1999) Abstract
2000
Section V. Application of Chimeras in Monitoring and Manipulating Cell Physiology-37 Use of Fusions to Green Fluorescent Protein in the Detection of Apoptosis, Shinbrot, Eve, Spencer Collin, Natale Valerie, and Kain Steven R. , Methods in Enzymology, Volume 327, p.513–521, (2000)
Use of fusions to green fluorescent protein in the detection of apoptosis., Shinbrot, Eve, Spencer Collin, Natale Valerie, and Kain Steven R. , Methods in enzymology, Volume 327, p.513, (2000)
Haplotypes at ATM identify coding-sequence variation and indicate a region of extensive linkage disequilibrium., Bonnen, P. E., Story M. D., Ashorn C. L., Buchholz T. A., Weil M. M., and Nelson D. L. , American journal of human genetics, 2000 Dec, Volume 67, Issue 6, p.1437-51, (2000) Abstract
A BAC-based physical map of the major autosomes of Drosophila melanogaster., Hoskins, R. A., Nelson C. R., Berman B. P., Laverty T. R., George R. A., Ciesiolka L., Naeemuddin M., Arenson A. D., Durbin J., David R. G., et al. , Science (New York, N.Y.), 2000 Mar 24, Volume 287, Issue 5461, p.2271-4, (2000) Abstract
The genome sequence of Drosophila melanogaster., Adams, M. D., Celniker S. E., Holt R. A., Evans C. A., Gocayne J. D., Amanatides P. G., Scherer S. E., Li P. W., Hoskins R. A., Galle R. F., et al. , Science (New York, N.Y.), 2000 Mar 24, Volume 287, Issue 5461, p.2185-95, (2000) Abstract
Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10., Matsuura, T., Yamagata T., Burgess D. L., Rasmussen A., Grewal R. P., Watase K., Khajavi M., McCall A. E., Davis Caleb F., Zu L., et al. , Nature genetics, 2000 Oct, Volume 26, Issue 2, p.191-4, (2000) Abstract
Enterococcus faecalis adhesin, ace, mediates attachment to extracellular matrix proteins collagen type IV and laminin as well as collagen type I., Nallapareddy, S. R., Qin X., Weinstock G. M., Höök M., and Murray B. E. , Infection and immunity, 2000 Sep, Volume 68, Issue 9, p.5218-24, (2000) Abstract
Enterococcus faecalis adhesin, ace, mediates attachment to extracellular matrix proteins collagen type IV and laminin as well as collagen type I., Nallapareddy, S. R., Qin X., Weinstock G. M., Höök M., and Murray B. E. , Infection and immunity, 2000 Sep, Volume 68, Issue 9, p.5218-24, (2000) Abstract


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