M. Jong

发表

Adhesion-promoting receptors on human macrophages recognize Escherichia coli by binding to lipopolysaccharide

S. Wright, M. Jong, Michelle T. C. Jong, 1986, The Journal of experimental medicine.

Gene structure, DNA methylation, and imprinted expression of the human SNRPN gene.

D. J. Driscoll, U. Surti, S. Saitoh, 1996, American journal of human genetics.

The homeodomain protein, Pit-1/GHF-1, is capable of binding to and activating cell-specific elements of both the growth hormone and prolactin gene promoters.

S. R. Fox, H. Samuels, F. Stanley, 1990, Molecular endocrinology.

Multiple imprinted genes associated with Prader-Willi syndrome and location of an imprinting control element.

D. J. Driscoll, S. Saitoh, P. Rogan, 1996, Acta geneticae medicae et gemellologiae.

C3bi receptor (complement receptor type 3) recognizes a region of complement protein C3 containing the sequence Arg-Gly-Asp.

B. W. Erickson, S. Wright, M. Jong, 1987, Proceedings of the National Academy of Sciences of the United States of America.

Interferon-gamma depresses binding of ligand by C3b and C3bi receptors on cultured human monocytes, an effect reversed by fibronectin

S. Wright, P. Detmers, M. Jong, 1986, The Journal of experimental medicine.

Organization and sequence of the human P gene and identification of a new family of transport proteins.

R. Spritz, R. Nicholls, S. T. Lee, 1995, Genomics.

A gene for the mouse pink-eyed dilution locus and for human type II oculocutaneous albinism

R. Spritz, B. Horsthemke, R. Nicholls, 1993, Nature.

A sequence in the rat Pit-1 gene promoter confers synergistic activation by glucocorticoids and protein kinase-C.

B M Raaka, H H Samuels, B. Raaka, 1994, Molecular endocrinology.

A novel imprinted gene, encoding a RING zinc-finger protein, and overlapping antisense transcript in the Prader-Willi syndrome critical region.

D. J. Driscoll, S. Saitoh, Y. Ji, 1999, Human molecular genetics.

Imprinting of a RING zinc-finger encoding gene in the mouse chromosome region homologous to the Prader-Willi syndrome genetic region.

D. J. Driscoll, M. Handel, K. Caldwell, 1999, Human molecular genetics.

Functional imprinting and epigenetic modification of the human SNRPN gene.

D. J. Driscoll, R. Nicholls, C. Glenn, 1993, Human molecular genetics.

CR3 (CD11b/CD18) expresses one binding site for Arg-Gly-Asp-containing peptides and a second site for bacterial lipopolysaccharide

S. Wright, Z. Chad, L. Kabbash, 1989, The Journal of experimental medicine.