Aviram Kogot-Levin

发表

Mucolipidosis type IV and the mucolipins.

D. Zeevi, A. Frumkin, G. Bach, 2010, Biochemical Society transactions.

A potentially dynamic lysosomal role for the endogenous TRPML proteins

D. Zeevi, A. Frumkin, G. Bach, 2009, The Journal of pathology.

Ablation of Ceramide Synthase 2 Causes Chronic Oxidative Stress Due to Disruption of the Mitochondrial Respiratory Chain*

A. Scherz, A. Merrill, Ann Saada, 2013, The Journal of Biological Chemistry.

The Thr224Asn mutation in the VPS45 gene is associated with the congenital neutropenia and primary myelofibrosis of infancy.

A. Borkhardt, D. Mevorach, U. Fischer, 2013, Blood.

Opposite physiological and pathological mTORC1-mediated roles of the CB1 receptor in regulating renal tubular function

B. Thorens, G. Leibowitz, J. Gertsch, 2022, Nature Communications.

Proximal Tubule mTORC1 Is a Central Player in the Pathophysiology of Diabetic Nephropathy and Its Correction by SGLT2 Inhibitors

B. Tirosh, E. Cerasi, G. Leibowitz, 2020, Cell reports.

Protection of a Ceramide Synthase 2 Null Mouse from Drug-induced Liver Injury

A. Merrill, B. Tirosh, Ann Saada, 2013, The Journal of Biological Chemistry.

PHAGOCYTES, GRANULOCYTES, AND MYELOPOIESIS The Thr224Asn mutation in the VPS45 gene is associated with the congenital neutropenia and primary myelo ﬁ brosis of infancy

A. Borkhardt, D. Mevorach, U. Fischer, 2013 .

Development of pheochromocytoma in ceramide synthase 2 null mice.

A. Merrill, Ann Saada, A. Futerman, 2015, Endocrine-related cancer.

The influence of in vivo exposure to nonylphenol ethoxylate 10 (NP-10) on the ovarian reserve in a mouse model.

B. Fisch, Ann Saada, Y. Shufaro, 2018, Reproductive toxicology.

Combined mineralocorticoid and glucocorticoid deficiency is caused by a novel founder nicotinamide nucleotide transhydrogenase mutation that alters mitochondrial morphology and increases oxidative stress

L. Carmel, E. Levy-Lahad, D. Zangen, 2015, Journal of Medical Genetics.

Ceramide and the mitochondrial respiratory chain.

Ann Saada, Aviram Kogot-Levin, 2014, Biochimie.

Upregulation of Mitochondrial Content in Cytochrome c Oxidase Deficient Fibroblasts

Ann Saada, G. Leibowitz, I. Raz, 2016, PloS one.

Pathogenesis of diabesity‐induced kidney disease: role of kidney nutrient sensing

G. Leibowitz, J. Tam, Aviram Kogot-Levin, 2021, The FEBS journal.

Mapping the metabolic reprogramming induced by sodium-glucose cotransporter 2 inhibition

E. Gottlieb, E. Bernal-Mizrachi, E. Cerasi, 2023, JCI insight.

Encephalopathy Caused by Ablation of Very Long Acyl Chain Ceramide Synthesis May Be Largely Due to Reduced Galactosylceramide Levels*

J. Alroy, I. Biton, A. Merrill, 2011, The Journal of Biological Chemistry.

Hyperglucagonaemia in diabetes: altered amino acid metabolism triggers mTORC1 activation, which drives glucagon production

B. Glaser, E. Gottlieb, E. Bernal-Mizrachi, 2023, Diabetologia.

Mucolipidosis Type IV: The Effect of Increased Lysosomal pH on the Abnormal Lysosomal Storage

A. Ornoy, G. Bach, M. Zeigler, 2009, Pediatric Research.

Ablation of Ceramide Synthase 2 Causes Chronic Oxidative Stress Due to Disruption of the Mitochondrial Respiratory Chain*

A. Scherz, A. Merrill, Ann Saada, 2013, The Journal of Biological Chemistry.

Combined mineralocorticoid and glucocorticoid deficiency is caused by a novel founder nicotinamide nucleotide transhydrogenase mutation that alters mitochondrial morphology and increases oxidative stress

L. Carmel, E. Levy-Lahad, D. Zangen, 2015, Journal of Medical Genetics.

A potentially dynamic lysosomal role for the endogenous TRPML proteins

D. Zeevi, A. Frumkin, G. Bach, 2009, The Journal of pathology.