A. Snowden

发表

Animal Lectins as Self/Non‐Self Recognition Molecules

H. Ahmed, G. Vasta, A. Marsh, 1994, Annals of the New York Academy of Sciences.

Redox-regulated Signaling by Lactosylceramide in the Proliferation of Human Aortic Smooth Muscle Cells*

A. Bhunia, S. Chatterjee, A. Snowden, 1997, The Journal of Biological Chemistry.

Oxidized low density lipoproteins stimulate galactosyltransferase activity, ras activation, p44 mitogen activated protein kinase and c-fos expression in aortic smooth muscle cells.

A. Bhunia, S. Chatterjee, H. Han, 1997, Glycobiology.

Nonsense suppressor therapies rescue peroxisome lipid metabolism and assembly in cells from patients with specific PEX gene mutations

J. Hacia, Nathan Oesch, N. Braverman, 2011, Journal of cellular biochemistry.

Lactosylceramide Stimulates Ras-GTP Loading, Kinases (MEK, Raf), p44 Mitogen-activated Protein Kinase, and c-fos Expression in Human Aortic Smooth Muscle Cells (*)

A. Bhunia, S. Chatterjee, A. Snowden, 1996, The Journal of Biological Chemistry.

X-linked adrenoleukodystrophy in a chimpanzee due to an ABCD1 mutation reported in multiple unrelated humans.

A. Moser, F. Eichler, A. Vanderver, 2017, Molecular genetics and metabolism.

Oxidized low density lipoproteins stimulate galactosyltransferase activity , ras activation , p 44 mitogen activated protein kinase and c-fos expression in aortic smooth muscle cells

A. Bhunia, S. Chatterjee, Hui-Jing Han, 2005 .

The peroxisomal AAA ATPase complex prevents pexophagy and development of peroxisome biogenesis disorders

A. Moser, N. Braverman, P. Kim, 2017, Autophagy.

Recovery of PEX1-Gly843Asp peroxisome dysfunction by small-molecule compounds

S. Jiralerspong, N. Braverman, S. Steinberg, 2010, Proceedings of the National Academy of Sciences.

X-linked adrenoleukodystrophy: ABCD1 de novo mutations and mosaicism.

A. Moser, G. Raymond, C. Reeves, 2011, Molecular genetics and metabolism.

A PEX10 defect in a patient with no detectable defect in peroxisome assembly or metabolism in cultured fibroblasts

H. Moser, A. Moser, G. Raymond, 2009, Journal of Inherited Metabolic Disease.

Functional characterization of novel mutations in GNPAT and AGPS, causing rhizomelic chondrodysplasia punctata (RCDP) types 2 and 3

A. Moser, S. Jiralerspong, N. Braverman, 2012, Human mutation.

Distribution of Choline Acetyltransferase in Cerebral and Extracerebral Cranial Arteries of the Cat: Its Relationship to Neurogenic Atropine‐Sensitive Dilation

J. Bevan, G. Buga, V. Florence, 1982, Circulation research.

Nonsense suppressor therapies rescue peroxisome lipid metabolism and assembly in cells from patients with specific PEX gene mutations

J. Hacia, Nathan Oesch, N. Braverman, 2011, Journal of cellular biochemistry.