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8 results for author:"Stewart D.M." in Literature citations

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AOF1 is a histone H3K4 demethylase possessing demethylase activity-independent repression function.

Yang Z., Jiang J., Stewart D.M., Qi S., Yamane K., Li J., Zhang Y., Wong J.

Cell Res. 20:276-287(2010) · Mapped (2)

Mutations of the Wiskott-Aldrich Syndrome Protein (WASP): hotspots, effect on transcription, and translation and phenotype/genotype correlation.

Jin Y., Mazza C., Christie J.R., Giliani S., Fiorini M., Mella P., Gandellini F., Stewart D.M., Zhu Q., Nelson D.L. et al.

Blood 104:4010-4019(2004) · Mapped (3)

AKAP350 interaction with cdc42 interacting protein 4 at the Golgi apparatus.

Larocca M.C., Shanks R.A., Tian L., Nelson D.L., Stewart D.M., Goldenring J.R.

Mol. Biol. Cell 15:2771-2781(2004) · UniProtKB (3)

Altered gene expression pattern in cultured human breast cancer cells treated with hepatocyte growth factor/scatter factor in the setting of DNA damage.

Yuan R.-Q., Fan S., Achary M., Stewart D.M., Goldberg I.D., Rosen E.M.

Cancer Res. 61:8022-8031(2001) · UniProtKB (1)

A complex of N-WASP and WIP integrates signalling cascades that lead to actin polymerization.

Moreau V., Frischknecht F., Reckmann I., Vincentelli R., Rabut G., Stewart D.M., Way M.

Nat. Cell Biol. 2:441-448(2000) · UniProtKB (1)

Cdc42-interacting protein 4 mediates binding of the Wiskott-Aldrich syndrome protein to microtubules.

Tian L., Nelson D.L., Stewart D.M.

J. Biol. Chem. 275:7854-7861(2000) · UniProtKB (1) · Mapped (2)

Mutations that cause the Wiskott-Aldrich syndrome impair the interaction of Wiskott-Aldrich syndrome protein (WASP) with WASP interacting protein.

Stewart D.M., Tian L., Nelson D.L.

J. Immunol. 162:5019-5024(1999) · UniProtKB (1)

Defective actin polymerization in EBV-transformed B-cell lines from patients with the Wiskott-Aldrich syndrome.

Facchetti F., Blanzuoli L., Vermi W., Notarangelo L.D., Giliani S., Fiorini M., Fasth A., Stewart D.M., Nelson D.L.

J. Pathol. 185:99-107(1998) · UniProtKB (1)

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