N. Dracopoli

发表

A genetic map of the mouse suitable for typing intraspecific crosses.

E S Lander, E. Lander, S. Lincoln, 1992, Genetics.

J. Haines, J. Attwood, J. Gusella, 1994, Genomics.

A genetic linkage map of 27 loci from PND to FY on the short arm of human chromosome I.

E. Lander, S. Lincoln, D. Housman, 1988, American journal of human genetics.

Branched chain acyltransferase absence due to an Alu-based genomic deletion allele and an exon skipping allele in a compound heterozygote proband expressing maple syrup urine disease.

D. Danner, N. Dracopoli, W. J. Herring, 1992, Biochimica et biophysica acta.

Rapid physical mapping of cloned DNA on banded mouse chromosomes by fluorescence in situ hybridization.

D. Housman, D. Ward, N. Dracopoli, 1992, Genomics.

Familial hypothyroidism caused by a nonsense mutation in the thyroid-stimulating hormone beta-subunit gene.

I. Kourides, D. Feltquate, C. Dacou-voutetakis, 1990, American journal of human genetics.

Identification of a new murine runt domain-containing gene, Cbfa3, and localization of the human homolog, CBFA3, to chromosome 1p35-pter.

Ping Liu, C. Wijmenga, F. Collins, 1995, Genomics.

Probe 8B/E5' detects a second RFLP at the human liver/bone/kidney alkaline phosphatase (ALPL) locus.

H. Harris, M. Weiss, K. Ray, 1988, Nucleic acids research.

Assignment of the gene for the beta subunit of thyroid-stimulating hormone to the short arm of human chromosome 1.

L. Old, G. Darlington, I. Kourides, 1986, Proceedings of the National Academy of Sciences of the United States of America.

Antigens Expressed by Melanoma and Melanocytes

A. Houghton, A. Albino, N. Dracopoli, 1987 .

Genes controlling gp25/30 cell-surface molecules map to chromosomes X and Y and escape X-inactivation.

N. Archidiacono, M. Rocchi, D. Esposito, 1985, American journal of human genetics.

Somatic cell genetic analysis of human cell surface antigens: chromosomal assignments and regulation of expression in rodent-human hybrid cells.

L. Old, H. Oettgen, B. Spengler, 1984, Proceedings of the National Academy of Sciences of the United States of America.

A PCR-based linkage map of human chromosome 1.

J. Weber, L. Peltonen, T. Hudson, 1993, Genomics.

Three human cell surface antigen systems determined by genes on chromosome 12

A. Houghton, L. Old, H. Oettgen, 1984, Somatic cell and molecular genetics.

Loss of polymorphic restriction fragments in malignant melanoma: implications for tumor heterogeneity.

A. Houghton, L. Old, N. Dracopoli, 1985, Proceedings of the National Academy of Sciences of the United States of America.

Two thyroid hormone regulated genes, the beta-subunits of nerve growth factor (NGFB) and thyroid stimulating hormone (TSHB), are located less than 310 kb apart in both human and mouse genomes.

D. Housman, I. Kourides, E. Rose, 1988, Genomics.

The CEPH consortium linkage map of human chromosome 1.

R L White, K H Buetow, J M Lalouel, 1991, Genomics.

Role of human chromosome 11 in determining surface antigenic phenotype of normal and malignant cells. Somatic cell genetic analysis of eight antigens, including putative human Thy-1

L. Old, H. Beresford, B. Spengler, 1985, The Journal of experimental medicine.

Mapping the human amylase gene cluster on the proximal short arm of chromosome 1 using a highly informative (CA)n repeat.

M. Meisler, N. Dracopoli, 1990, Genomics.

Evidence for human meiotic recombination interference obtained through construction of a short tandem repeat-polymorphism linkage map of chromosome 19.

J. Weber, B. Keats, Z. Wang, 1993, American journal of human genetics.

Isolation and chromosomal assignment of 100 highly informative human simple sequence repeat polymorphisms.

T. Hudson, D. Housman, M. Rubenfield, 1992, Genomics.

The IPP gene is assigned to human chromosome 1p32-1p22.

E. Jabs, R. Huang, X. Li, 1993, Genomics.

Loss of heterozygosity at autosomal and X-linked loci during tumor progression in a patient with melanoma.

A. Houghton, L. Old, N. Dracopoli, 1987, Cancer research.

Genetic and physical map of the interferon region on chromosome 9p.

D. Housman, D. Ward, M. Karayiorgou, 1992, Genomics.

Localization of the FGR protooncogene on the genetic linkage map of human chromosome 1p.

D. Housman, B. Stanger, N. Dracopoli, 1988, Genomics.

Restriction analysis of the structural alpha-L-fucosidase gene and its linkage to fucosidosis.

E. Wijsman, D. Gerhard, D. Housman, 1988, American journal of human genetics.

Optimized conditions for cloning PCR products into an XcmI T-vector.

B. Schutte, K. Ranade, N. Dracopoli, 1997, BioTechniques.

Integration of gene maps: chromosome 1.

N E Morton, D C Shields, B J Keats, 1992, Proceedings of the National Academy of Sciences of the United States of America.