Theodore C. Iancu

24 Hazevi Avenue
Haifa, HA 34355, Israel

Last Updated: 09/26/2026

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Found 11 publications

ATP6AP1 deficiency causes an immunodeficiency with hepatopathy, cognitive impairment and abnormal protein glycosylation.

ATP6AP1 deficiency causes an immunodeficiency with hepatopathy, cognitive impairment and abnormal protein glycosylation.

Journal: Nature communications

Published: July 27, 2015

Fat malabsorption due to bile acid synthesis defect.

Fat malabsorption due to bile acid synthesis defect.

Journal: The Israel Medical Association journal : IMAJ

Published: May 08, 2015

Iron-rich ferritin in the hypoxia-tolerant rodent Spalax ehrenbergi: a naturally-occurring biomarker confirms the internalization and pathways of intracellular macromolecules.

Iron-rich ferritin in the hypoxia-tolerant rodent Spalax ehrenbergi: a naturally-occurring biomarker confirms the internalization and pathways of intracellular macromolecules.

Journal: Journal of structural biology

Published: March 07, 2014

What's in a name?-"Lipolysosome": ultrastructural features of a lipid-containing organelle.

What's in a name?-"Lipolysosome": ultrastructural features of a lipid-containing organelle.

Journal: Ultrastructural pathology

Published: September 20, 2013

Pronounced cancer resistance in a subterranean rodent, the blind mole-rat, Spalax: in vivo and in vitro evidence.

Pronounced cancer resistance in a subterranean rodent, the blind mole-rat, Spalax: in vivo and in vitro evidence.

Journal: BMC biology

Published: April 18, 2013

Infantile mitochondrial hepatopathy is a cardinal feature of MEGDEL syndrome (3-methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and Leigh-like syndrome) caused by novel mutations in SERAC1.

Infantile mitochondrial hepatopathy is a cardinal feature of MEGDEL syndrome (3-methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and Leigh-like syndrome) caused by novel mutations in SERAC1.

Journal: American journal of medical genetics. Part A

Published: September 14, 2012

Poor lysosomal membrane integrity in proximal tubule cells of haptoglobin 2-2 genotype mice with diabetes mellitus.

Poor lysosomal membrane integrity in proximal tubule cells of haptoglobin 2-2 genotype mice with diabetes mellitus.

Journal: Free radical biology & medicine

Published: March 22, 2012

Effects of novel neuroprotective and neurorestorative multifunctional drugs on iron chelation and glucose metabolism.

Effects of novel neuroprotective and neurorestorative multifunctional drugs on iron chelation and glucose metabolism.

Journal: Journal of neural transmission (Vienna, Austria : 1996)

Published: January 19, 2012

Ultrastructural aspects of iron storage, transport and metabolism.

Ultrastructural aspects of iron storage, transport and metabolism.

Journal: Journal of neural transmission (Vienna, Austria : 1996)

Published: August 26, 2010

Ultrastructural aspects of enterocyte defects in infancy and childhood.

Ultrastructural aspects of enterocyte defects in infancy and childhood.

Journal: Ultrastructural pathology

Published: May 12, 2010

The liver in congenital disorders of glycosylation: ultrastructural features.

The liver in congenital disorders of glycosylation: ultrastructural features.

Journal: Ultrastructural pathology

Published: July 07, 2007

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Last Updated: 09/26/2026