The mutagenic activity of razoxane (ICRF 159): an anticancer agent.

Por Albanese, R., Watkins, P. A.
Publicado em 1985

PXA1, a possible Saccharomyces cerevisiae ortholog of the human adrenoleukodystrophy gene.

Por Shani, N, Watkins, P A, Valle, D
Publicado em 1995

Inhibition of the GTPase activity of transducin by an NAD+:arginine ADP-ribosyltransferase from turkey erythrocytes.

Por Watkins, P A, Kanaho, Y, Moss, J
Publicado em 1987

Mechanism for acute control of fatty acid synthesis by glucagon and 3':5'-cyclic AMP in the liver cell.

Por Watkins, P A, Tarlow, D M, Lane, M D
Publicado em 1977

Direct recovery of in vitro transcripts in a protected form suitable for prolonged storage and shipment at ambient temperatures.

Por Jupin, I, Sleat, D E, Watkins, P A, Wilson, T M
Publicado em 1989

Peroxisomal beta-oxidation enzyme proteins in adrenoleukodystrophy: distinction between X-linked adrenoleukodystrophy and neonatal adrenoleukodystrophy.

Por Chen, W W, Watkins, P A, Osumi, T, Hashimoto, T, Moser, H W
Publicado em 1987

Metabolism of Inositol(1,4,5)trisphosphate by a Soluble Enzyme Fraction from Pea (Pisum sativum) Roots

Por Drøbak, B. K., Watkins, P. A. C., Chattaway, J. A., Roberts, K., Dawson, A. P.
Publicado em 1991

Role of ALDP (ABCD1) and Mitochondria in X-Linked Adrenoleukodystrophy

Por McGuinness, M. C., Lu, J.-F., Zhang, H.-P., Dong, G.-X., Heinzer, A. K., Watkins, P. A., Powers, J., Smith, K. D.
Publicado em 2003

Altered expression of ALDP in X-linked adrenoleukodystrophy.

Por Watkins, P A, Gould, S J, Smith, M A, Braiterman, L T, Wei, H M, Kok, F, Moser, A B, Moser, H W, Smith, K D
Publicado em 1995

A New Genetic Disorder in Mitochondrial Fatty Acid β-Oxidation: ACAD9 Deficiency

Por He, M. , Rutledge, S. L. , Kelly, D. R. , Palmer, C. A. , Murdoch, G. , Majumder, N. , Nicholls, R. D. , Pei, Z. , Watkins, P. A. , Vockley, J. 
Publicado em 2007

Peroxisomal bifunctional enzyme deficiency.

Por Watkins, P A, Chen, W W, Harris, C J, Hoefler, G, Hoefler, S, Blake, D C, Balfe, A, Kelley, R I, Moser, A B, Beard, M E
Publicado em 1989

Peroxisomal bifunctional protein deficiency revisited: resolution of its true enzymatic and molecular basis.

Por van Grunsven, E G, van Berkel, E, Mooijer, P A, Watkins, P A, Moser, H W, Suzuki, Y, Jiang, L L, Hashimoto, T, Hoefler, G, Adamski, J, Wanders, R J
Publicado em 1999