Kurt J. Isselbacher

msg1, a novel melanocyte-specific gene, encodes a nuclear protein and is associated with pigmentation.

K. Isselbacher, T. Shioda, M. Fenner, 1996, Proceedings of the National Academy of Sciences of the United States of America.

Increased expression of eukaryotic translation initiation factors eIF-4E and eIF-2 alpha in response to growth induction by c-myc.

K. Isselbacher, E. Schmidt, I. Rosenwald, 1993, Proceedings of the National Academy of Sciences of the United States of America.

An increased risk of Crohn's disease in individuals who inherit the HLA class II DRB3*0301 allele.

K. Isselbacher, D. Podolsky, D. Forcione, 1996, Proceedings of the National Academy of Sciences of the United States of America.

Galactosemia, a congenital defect in a nucleotide transferase.

E. P. Anderson, K. Isselbacher, H. Kalckar, 1956, Biochimica et biophysica acta.

Genetic susceptibility to breast cancer: HLA DQB*03032 and HLA DRB1*11 may represent protective alleles.

K. Isselbacher, D. Haber, D. Bell, 2000, Proceedings of the National Academy of Sciences of the United States of America.

Defect in uptake of galactose-1-phosphate into liver nucleotides in congenital galactosemia.

E. P. Anderson, K. Isselbacher, H. Kalckar, 1957, Science.

Photoaffinity labeling of the stereospecific D-glucose transport system with cytochalasin B.

K. Isselbacher, M. Czech, J. Pessin, 1984, Federation proceedings.

Partial suppression of anchorage-independent growth and tumorigenicity in immunodeficient mice by transfection of the H-2 class I gene H-2Ld into a human colon cancer cell line (HCT).

K. Isselbacher, C. Willett, K. Kirsch, 1988, Proceedings of the National Academy of Sciences of the United States of America.