C. Collins

Identification of a common PEX1 mutation in Zellweger syndrome

S. Gould, C. Collins, 1999, Human mutation.

Disruption of a PEX1-PEX6 interaction is the most common cause of the neurologic disorders Zellweger syndrome, neonatal adrenoleukodystrophy, and infantile Refsum disease.

B. Geisbrecht, S. Gould, B. E. Reuber, 1998, Proceedings of the National Academy of Sciences of the United States of America.

In Vitro Site-Specific Incorporation of Fluorescent Probes into β-Galactosidase

A. Chamberlin, Marcella A. Gilmore, Justin E. Carlson, 1997 .

The Peroxisome Biogenesis Factors Pex4p, Pex22p, Pex1p, and Pex6p Act in the Terminal Steps of Peroxisomal Matrix Protein Import

J. McCaffery, S. Gould, Cynthia S. Collins, 2000, Molecular and Cellular Biology.

Mutations in PEX1 are the most common cause of peroxisome biogenesis disorders

H. Moser, D. Valle, S. Gould, 1997, Nature Genetics.

A small interfering RNA screen for modulators of tumor cell motility identifies MAP4K4 as a promigratory kinase.

Yingyao Zhou, L. Sapinoso, G. Hampton, 2006, Proceedings of the National Academy of Sciences of the United States of America.

Peroxisomal-protein import: is it really that complex?

S. Gould, C. Collins, 2002, Nature Reviews Molecular Cell Biology.

A small interfering RNA screen for modulators of tumor cell motility identifies MAP4K4 as a promigratory kinase.

Yingyao Zhou, L. Sapinoso, G. Hampton, 2006, Proceedings of the National Academy of Sciences of the United States of America.