K. Lomax

发表

Genes for two autosomal recessive forms of chronic granulomatous disease assigned to 1q25 (NCF2) and 7q11.23 (NCF1).

U. Francke, C. Hsieh, B. Foellmer, 1990, American journal of human genetics.

Cloning and functional expression of the mouse homologue of p47phox

S. Holland, C. Kozak, H. Malech, 2004, Immunogenetics.

Studies of Gene Expression During Granulocyte Maturation

C. Stolle, J. Schneider, K. High, 1987 .

Expression of multiple Na+,K+-adenosine triphosphatase isoform genes in human hematopoietic cells. Behavior of the novel A3 isoform during induced maturation of HL60 cells.

C. Stolle, J. Schneider, E. Benz, 1989, The Journal of clinical investigation.

Selective defect in myeloid cell lactoferrin gene expression in neutrophil specific granule deficiency.

M. Kaliner, D. Rotrosen, L. Boxer, 1989, The Journal of clinical investigation.

Cloning of a 67-kD neutrophil oxidase factor with similarity to a noncatalytic region of p60c-src.

H. Malech, W. Nauseef, T. Leto, 1990, Science.

Recombinant 47-kilodalton cytosol factor restores NADPH oxidase in chronic granulomatous disease.

H. Malech, T. Leto, J. Gallin, 1989, Science.

Minor errors in two published sequences.

H. Malech, T. Leto, J. Gallin, 1989, Science.

The molecular biology of selected phagocyte defects.

J. Gallin, H. Malech, K. Lomax, 1989, Blood reviews.

Retroviral expression of recombinant p47phox protein by Epstein-Barr virus-transformed B lymphocytes from a patient with autosomal chronic granulomatous disease.

R. Blaese, H. Malech, T. Leto, 1992, Blood.