Results 101 to 110 of about 1,418 (198)

Alternative splicing in the Atp7a gene in the Cu deficient mosaic mutation in mice [PDF]

, 2004
Grzmil, Paweł, Lenartowicz, Małgorzata, Rusin, Marek, Styrna, Józefa   +3 more
core  

A Case of Infantile Reversible Cytochrome C Oxidase Deficiency Myopathy in Taiwan: A 4-Year Follow-Up. [PDF]

Case Rep Med
Ma YT, Lin JL, Lai MW, Chou IJ, Hwang MS.   +4 more
europepmc   +1 more source

Studies of the copper binding protein in the small intestinal membrane of black Agouti mice, 1983 [PDF]

core   +1 more source

Disorders of Copper Metabolism in Children-A Problem too Rarely Recognized. [PDF]

Metabolites
Więcek S, Paprocka J.
europepmc   +1 more source

Hair Shaft Fracture in a Young Athlete: A Rare Case Report of Acquired Trichorrhexis Nodosa. [PDF]

Cureus
S A, R G S, C R V N, D SK, Geeta Sai G.
europepmc   +1 more source

Elesclomol rescues mitochondrial copper deficiency in disease models without triggering cuproptosis. [PDF]

J Pharmacol Exp Ther
Zulkifli M, Maremanda KP, Okonkwo AU, Farid I, Gohil VM.   +4 more
europepmc   +1 more source

Copper, Cuproptosis, and Neurodegenerative Diseases. [PDF]

Int J Mol Sci
Genchi G, Catalano A, Carocci A, Sinicropi MS, Lauria G.   +4 more
europepmc   +1 more source

Menkes' disease: case report [PDF]

Aicardi J, Amato AA, Ana C.S. Crippa, Bankier A, Carlos E. Silvado, Chelly J, Fabio Agertt, Gu YH, Guitet M, Isac Bruck, Jacobs DS, Jayawant S, Kaler SG, Kodama H, Lineu C. Werneck, Luciano de Paola, Mandelstam SA, Menkes JH, Meyer BU, Morgello S, Paulo J. Lorenzoni, Pedespan JM, Rosana H. Scola, Santos LMG, Venta-Sobero JA, Voskoboinik I, Vulpe C, Vulpe CD, Werneck LC, White SR   +29 more
core   +1 more source

Copper in Human Health and Disease: Insights from Inherited Disorders. [PDF]

Physiology (Bethesda)
Petruzzelli R, Polishchuk E, Polishchuk R.   +2 more
europepmc   +1 more source