K. H. Choo

发表

Molecular cloning of the gene for human anti-haemophilic factor IX

D. Rees, G. Brownlee, K. Gould, 1982, Nature.

LINKAGE ANALYSIS OF X-LINKED MENTAL RETARDATION WITH AND WITHOUT FRAGILE-X USING FACTOR IX GENE PROBE

M. Leversha, D. Danks, J. Halliday, 1984, The Lancet.

Cosmid vectors for high efficiency DNA-mediated transformation and gene amplification in mammalian cells: studies with the human growth hormone gene.

Y. Kan, Y. Lau, S. Greco, 1986, Gene.

Application of DNA-DNA hybridization of dual labeled probes to the detection of trisomy 21, monosomy 21, and sex determination.

D. Danks, H. Dahl, K. H. Choo, 1988, American journal of human genetics.

Genetics of the mammalian phenylalanine hydroxylase system. Studies of human liver phenylalanine hydroxylase subunit structure and of mutations in phenylketonuria.

R. Cotton, D. Danks, I. Jennings, 1979, The Biochemical journal.

Phenylalanine hydroxylation and tyrosine requirement of cultured cells. Evidence of phenylalanine hydroxylation in mastocytoma cells in culture.

R. Cotton, D. Danks, K. H. Choo, 1976, Experimental cell research.

Assignment of the haemophilia B (Factor IX) locus to the q26‐qter region of the X chromosome

B. Migeon, I. Craig, Y. Boyd, 1984, Annals of human genetics.

The gene structure of human anti‐haemophilic factor IX.

D. Rees, G. Brownlee, K. Gould, 1984, The EMBO journal.

CHARACTERISATION AND USE OF AN INTRAGENIC POLYMORPHIC MARKER FOR DETECTION OF CARRIERS OF HAEMOPHILIA B (FACTOR IX DEFICIENCY)

G. Brownlee, C. Rizza, F. Giannelli, 1984, The Lancet.

Gene deletions in patients with haemophilia B and anti-factor IX antibodies

D. Rees, G. Brownlee, C. Rizza, 1983, Nature.

Vectors for expression and amplification of cDNA in mammalian cells: expression of rat phenylalanine hydroxylase.

I. Jennings, K. Fowler, K. H. Choo, 1986, DNA.

Heterogeneity of the molecular defect in human dihydropteridine reductase deficiency.

R. Cotton, D. Danks, K. H. Choo, 1981, Biochemical Journal.

Genetics of the mammalian phenylalanine hydroxylase system. II. Immunological and two-dimensional gel electrophoretic studies of phenylalanine hydroxylase in cultured normal and mutant rat hepatoma cells

R. Cotton, K. H. Choo, 1979, Biochemical Genetics.

Genetics of the mammalian phenylalanine hydroxylase system. IV. Evidence of phenylalanine hydroxylase in a cultured human hepatoma cell line

R. Cotton, D. Danks, I. Jennings, 1980, Biochemical Genetics.

Genetics of the mammalian phenylalanine hydroxylase system: I. Isolation of phenylalanine hydroxylase-deficient tyrosine auxotrophs from rat hepatoma cells

R. Cotton, K. H. Choo, 1977, Somatic cell genetics.

Comparative studies of four monoclonal antibodies to phenylalanine hydroxylase exhibiting different properties with respect to substrate-dependence, species-specificity and a range of effects on enzyme activity.

R. Cotton, I. Jennings, K. H. Choo, 1981, The Biochemical journal.

Isolation and characterization of a myeloma--spleen-cell hybrid producing antibody to phenylalanine hydroxylase.

R. Cotton, I. Jennings, K. Fowler, 1980, The Biochemical journal.

Isolation of phenylalanine hydroxylase-stimulating monoclonal antibody by rat-myeloma--rat-spleen-cell fusion.

R. Cotton, D. Danks, J. Camakaris, 1980, The Biochemical journal.

Regional localisation of a non-specific X-linked mental retardation gene (MRX19) to Xp22.

A. Donnelly, J. Mulley, D. Danks, 1994, American journal of medical genetics.

Double-labeling and high precision comparison of complex protein patterns on two-dimensional polyacrylamide gels.

R. Cotton, D. Danks, K. H. Choo, 1980, Analytical biochemistry.