C. Jones

发表

Isolation and localization of DNA segments from specific human chromosomes.

D. Housman, J. Gusella, T. Puck, 1980, Proceedings of the National Academy of Sciences of the United States of America.

Regional localization of human extracellular superoxide dismutase gene to 4pter-q21.

Y. Ho, C. Jones, J. Fisher, 1990, Genomics.

The gene for the α2 chain of the human fibrillar collagen type XI (COL11A2) assigned to the short arm of chromosome 6

R. Berger, E. Solomon, C. Jones, 1990, Annals of human genetics.

Assignment of the gene for human sphingolipid activator protein-2 (SAP-2) to chromosome 10.

C. Jones, D. Wenger, F. Kao, 1985, American journal of human genetics.

Further changes in differentiation state accompanying the conversion of Chinese hamster cells of fibroblastic form by dibutyryl adenosine cyclic 3':5'-monophosphate and hormones.

T. Puck, A. Hsie, C. Jones, 1971, Proceedings of the National Academy of Sciences of the United States of America.

Isolation of 1001 new markers from human chromosome 11, excluding the region of 11p13-p15.5, and their sublocalization by a new series of radiation-reduced somatic cell hybrids.

D. Gerhard, N. Ma, E. Lawrence, 1992, Genomics.

Mammalian cell growth proteins. I. Growth stimulation of fetuin.

T. Puck, C. Waldren, C. Jones, 1968, Proceedings of the National Academy of Sciences of the United States of America.

Thirteen loci physically assigned to sheep Chromosome 2 by cell hybrid analysis and in situ hybridization

A. Gleeson, D. Burkin, C. Jones, 1995, Mammalian Genome.

Expression and reconstitution of a biologically active human interferon-gamma receptor in hamster cells.

C. Jones, V. Jung, C. Kumar, 1990, The Journal of biological chemistry.

Chromosomal assignment of the human erythropoietin gene and its DNA polymorphism.

C. H. Lin, F. Lin, C. Jones, 1986, Proceedings of the National Academy of Sciences of the United States of America.

Identification of two human ferritin H genes on the short arm of chromosome 6.

R. Benarous, C. Jones, G. Handelman, 1990, Genomics.

The gene for the human immune interferon receptor is located on chromosome 6.

J. Trill, J. Tischfield, H. Kung, 1986, Proceedings of the National Academy of Sciences of the United States of America.

Human chromosomes 6 and 21 are required for sensitivity to human interferon gamma.

T. Shows, J. Tischfield, A. Rashidbaigi, 1987, Proceedings of the National Academy of Sciences of the United States of America.

Atypical Down syndrome and partial trisomy 21

W. Brown, K. Wisniewski, C. Jones, 1983, Clinical genetics.

The coding sequence for the 32,000-dalton pulmonary surfactant-associated protein A is located on chromosome 10 and identifies two separate restriction-fragment-length polymorphisms.

R. Mason, C. Jones, F. Kao, 1987, American journal of human genetics.

Localization of the structural gene for human apolipoprotein A-I on the long arm of human chromosome 11.

T. Puck, L. Chan, C. Jones, 1984, Proceedings of the National Academy of Sciences of the United States of America.

Genetics of somatic mammalian cells: genetic, immunologic, and biochemical analysis with Chinese hamster cell hybrids containing selected human chromosomes.

T. Puck, C. Jones, F. Kao, 1976, Proceedings of the National Academy of Sciences of the United States of America.

Precise localization of human beta-globin gene complex on chromosome 11.

D. Housman, J. Gusella, T. Puck, 1979, Proceedings of the National Academy of Sciences of the United States of America.

Most Jacobsen syndrome deletion breakpoints occur distal to FRA11B.

E. Pivnick, A. Tunnacliffe, R. Michaelis, 1998, American journal of medical genetics.

Demonstration, by somatic cell genetics, of coordinate regulation of genes for two enzymes of purine synthesis assigned to human chromosome 21.

D. Patterson, S. Graw, C. Jones, 1981, Proceedings of the National Academy of Sciences of the United States of America.

Chromosome 3q (22-ter) encodes the human transferrin receptor.

C. Jones, P. Seligman, H. Morse, 1983, American journal of human genetics.

High-resolution meiotic and physical mapping of the best vitelliform macular dystrophy (VMD2) locus to pericentromeric chromosome 11.

H. Stöhr, D. Walker, C. Jones, 1994, American journal of human genetics.

Human aminoacylase-1: cloning, regional assignment to distal chromosome 3p21.1, and identification of a cross-hybridizing sequence on chromosome 18.

H. Drabkin, C. Jones, J. Fisher, 1990, Genomics.

Assignment of the gene coding for the T3-delta subunit of the T3-T-cell receptor complex to the long arm of human chromosome 11 and to mouse chromosome 9.

D. Gerhard, D. Housman, G. Bruns, 1985, Proceedings of the National Academy of Sciences of the United States of America.

Relationships between genes on human chromosome 11 encoding cell-surface antigens

P. Goodfellow, J. Bill, A. Tunnacliffe, 1984, Somatic cell and molecular genetics.

The use of cell surface antigens to characterize and select for fragments of human chromosomes retained by interspecies hybrids.

F. Ruddle, C. Jones, M. Kamarck, 1984, The Journal of experimental zoology.

A panel of irradiation-reduced hybrids selectively retaining human chromosome 11p13: their structure and use to purify the WAGR gene complex.

D. Housman, T. Glaser, E. Rose, 1990, Genomics.

Genetics of somatic mammalian cells: lethal antigens as genetic markers for study of human linkage groups.

T. Puck, C. Jones, F. Kao, 1971, Proceedings of the National Academy of Sciences of the United States of America.

Human gene locations achieved by means of human-Chinese hamster (CHO-K1) auxotrophic cell hybridization.

T. Puck, D. Patterson, F. Kao, 1976, Birth defects original article series.

11p15.5-specific libraries for identification of potential gene sequences involved in Beckwith-Wiedemann syndrome and tumorigenesis.

A. Ivens, P. Little, C. Jeanpierre, 1992, Genomics.

Two-dimensional electrophoresis of human-CHO cell hybrids containing human chromosome 11

T. Puck, D. Patterson, C. Jones, 1981, Somatic cell genetics.

Genetic analysis of human cell surface structures.

C. Jones, C. Jones, 1979, Haematology and blood transfusion.

The progesterone receptor gene maps to human chromosome band 11q13, the site of the mammary oncogene int-2.

T. Puck, B. O’Malley, G. Greene, 1987, Proceedings of the National Academy of Sciences of the United States of America.

Synteny between glycinamide ribonucleotide synthetase and superoxide dismutase (soluble).

C. Jones, F. Kao, E. Moore, 1977, American journal of human genetics.

Human T-cell receptor alpha-chain genes: location on chromosome 14.

E. Palmer, C. Jones, F. Kao, 1985, Science.

Assignment of the gene coding for phosphoribosylglycineamide formyltransferase to human chromosome 14

D. Patterson, C. Jones, F. Kao, 1981, Somatic cell genetics.

Chromosomal assignment of the gene for folylpolyglutamate synthetase to human chromosome 9.

R. Taylor, C. Jones, F. Kao, 1980, Cytogenetics and cell genetics.

Development of a somatic cell hybrid mapping panel and molecular probes for human chromosome 3.

H. Drabkin, M. Sage, S. Gold, 1990, Genomics.

Measurement of mutagenesis in mammalian cells.

T. Puck, C. Jones, C. Waldren, 1979, Proceedings of the National Academy of Sciences of the United States of America.

Localization of the photoreceptor gene ROM1 to human chromosome 11 and mouse chromosome 19: sublocalization to human 11q13 between PGA and PYGM.

D. Ledbetter, H. Willard, D. Gerhard, 1992, American journal of human genetics.

Human ferritin gene is assigned to chromosome 19.

C. Jones, P. Seligman, Y. Miller, 1983, Proceedings of the National Academy of Sciences of the United States of America.