N. Israelian

Highly variable clinical phenotype of carbamylphosphate synthetase 1 deficiency in one family: an effect of allelic variation in gene expression?

E. Christensen, J. Häberle, V. Klaus, 2009, Clinical genetics.

Sex Effects at the Ramparts: Nutrient- and Microbe-Mediated Regulation of the Immune-Metabolic Interface.

J. Danska, N. Israelian, 2017, Advances in experimental medicine and biology.

Deficiency of a Glycogen Synthase-associated Protein, Epm2aip1, Causes Decreased Glycogen Synthesis and Hepatic Insulin Resistance*

C. Ackerley, P. Frankland, A. Wheeler, 2013, The Journal of Biological Chemistry.

VMA21 deficiency prevents vacuolar ATPase assembly and causes autophagic vacuolar myopathy

J. Rilstone, C. Ackerley, I. Nishino, 2013, Acta Neuropathologica.

RETRACTED: VMA21 Deficiency Causes an Autophagic Myopathy by Compromising V-ATPase Activity and Lysosomal Acidification

J. Rilstone, C. Ackerley, I. Nishino, 2009, Cell.

VMA21 Deficiency Causes an Autophagic Myopathy by Compromising V-ATPase Activity and Lysosomal Acidification (Retracted article. See vol. 142, pg. 984, 2010)

J. Rilstone, C. Ackerley, I. Nishino, 2009 .

Behavioral evidence for photophobia and stress-related ipsilateral head pain in transgenic Cacna1a mutant mice

M. Ferrari, S. Spijker, A. M. van den Maagdenberg, 2013, PAIN®.

Retraction Notice to: VMA21 Deficiency Causes an Autophagic Myopathy by Compromising V-ATPase Activity and Lysosomal Acidification

J. Rilstone, C. Ackerley, I. Nishino, 2010, Cell.