Metabolic control of cell death

DR Green, L Galluzzi, G Kroemer - Science, 2014 - science.org
Background For several decades, intermediate metabolism and signal transduction have
been considered two independent entities. On one side stood the catabolic and anabolic …

Chemical composition of selected insect meals and their effect on apparent total tract digestibility, fecal metabolites, and microbiota of adult cats fed insect-based …

LM Reilly, Y Hu, PC Von Schaumburg… - Journal of animal …, 2022 - academic.oup.com
Insect meals are novel and potentially sustainable protein sources. The objectives of this
study were to determine the chemical composition and standardized amino acid digestibility …

[HTML][HTML] Exome sequence analysis suggests that genetic burden contributes to phenotypic variability and complex neuropathy

C Gonzaga-Jauregui, T Harel, T Gambin, M Kousi… - Cell reports, 2015 - cell.com
Summary Charcot-Marie-Tooth (CMT) disease is a clinically and genetically heterogeneous
distal symmetric polyneuropathy. Whole-exome sequencing (WES) of 40 individuals from 37 …

Ganglioside-induced differentiation associated protein 1 is a regulator of the mitochondrial network: new implications for Charcot-Marie-Tooth disease

A Niemann, M Ruegg, V La Padula… - The Journal of cell …, 2005 - rupress.org
Mutations in GDAP1 lead to severe forms of the peripheral motor and sensory neuropathy,
Charcot-Marie-Tooth disease (CMT), which is characterized by heterogeneous phenotypes …

Mitochondrial dynamics in diabetes

Y Yoon, CA Galloway, BS Jhun, T Yu - Antioxidants & redox …, 2011 - liebertpub.com
Mitochondria are at the center of cellular energy metabolism and regulate cell life and death.
The cell biological aspect of mitochondria, especially mitochondrial dynamics, has drawn …

Clinical and electrophysiological aspects of Charcot-Marie-Tooth disease

D Pareyson, V Scaioli, M Laura - Neuromolecular medicine, 2006 - Springer
Abstract Charcot-Marie-Tooth disease (CMT) is a genetically heterogeneous group of
disorders sharing the same clinical phenotype, characterized by distal limb muscle wasting …

Mutations in the HSP27 (HSPB1) gene cause dominant, recessive, and sporadic distal HMN/CMT type 2

H Houlden, M Laura, F Wavrant–De Vrièze, J Blake… - Neurology, 2008 - AAN Enterprises
Background: Charcot-Marie-Tooth disease (CMT) is the most common inherited
neuromuscular disorder and is characterized by significant clinical and genetic …

Mitochondrial dynamics and inherited peripheral nerve diseases

D Pareyson, P Saveri, A Sagnelli, G Piscosquito - Neuroscience letters, 2015 - Elsevier
Peripheral nerves have peculiar energetic requirements because of considerable length of
axons and therefore correct mitochondria functioning and distribution along nerves is …

Mutational screening of GDAP1 in dysphonia associated with Charcot-Marie-Tooth disease: clinical insights and phenotypic effects

U Manzoor, A Ali, SL Ali, O Abdelkarem… - Journal of Genetic …, 2023 - Elsevier
Abstract Introduction Mutations in GDAP1 (Ganglioside-induced differentiation-associated
protein 1) gene are linked to Charcot-Marie-Tooth disease (CMT), a Heterogenous group of …

GDAP1, the protein causing Charcot–Marie–Tooth disease type 4A, is expressed in neurons and is associated with mitochondria

L Pedrola, A Espert, X Wu, R Claramunt… - Human molecular …, 2005 - academic.oup.com
Mutations in GDAP1, the ganglioside-induced differentiation-associated protein 1 gene,
cause Charcot–Marie–Tooth (CMT) type 4A, a severe autosomal recessive form of …