Results 21 to 30 of about 46 (39)

Who Is Dermanyssus gallinae? Genetic Structure of Populations and Critical Synthesis of the Current Knowledge. [PDF]

Front Vet Sci, 2021
Roy L, Giangaspero A, Sleeckx N, Øines Ø.   +3 more
europepmc   +1 more source

Mitophagy in Human Diseases. [PDF]

Int J Mol Sci, 2021
Doblado L, Lueck C, Rey C, Samhan-Arias AK, Prieto I, Stacchiotti A, Monsalve M.   +6 more
europepmc   +1 more source

Relación entre el nivel de heteroplasmia de la mutación m.3243AG en diferentes tejidos y el fenotipo en familias con diabetes y sordera de herencia materna (midd) y melas

, 2015
El MELAS y la Diabetes y Sordera de Herencia Materna (MIDD) son enfermedades mitocondriales producidas en la mayor parte de los casos por una misma mutación: la m.3243AG, la cual afecta al gen MT-TL1. Esto muestra la gran variabilidad fenotípica de dicha mutación. Una de las posibles causas de esta variación puede ser el nivel de heteroplasmia de la
openaire   +1 more source

Heteroplasmia em Bombus morio (Hymenoptera, Apidae) e impactos em estudos evolutivos [PDF]

, 2018
openaire   +1 more source

New Variant of MELAS Syndrome With Executive Dysfunction, Heteroplasmic Point Mutation in the MT-ND4 Gene (m.12015T>C; p.Leu419Pro) and Comorbid Polyglandular Autoimmune Syndrome Type 2. [PDF]

Front Immunol, 2019
Endres D, Süß P, Maier SJ, Friedel E, Nickel K, Ziegler C, Fiebich BL, Glocker FX, Stock F, Egger K, Lange T, Dacko M, Venhoff N, Erny D, Doostkam S, Komlosi K, Domschke K, Tebartz van Elst L.   +17 more
europepmc   +1 more source

Long-term health of dopaminergic neuron transplants in Parkinson's disease patients. [PDF]

Cell Rep, 2014
Hallett PJ, Cooper O, Sadi D, Robertson H, Mendez I, Isacson O.   +5 more
europepmc   +1 more source

[Mitochondrial diabetes: From suspicion in primary care to a multidisciplinary family approach]. [PDF]

Aten Primaria
Macías Martínez BA, Dalmau Vila A, Hernández García M, Lafarga Giribets MA.   +3 more
europepmc   +1 more source

Rewriting nuclear epigenetic scripts in mitochondrial diseases as a strategy for heteroplasmy control. [PDF]

EMBO Mol Med
Pérez MJ, Colombo RB, Real SM, Branham MT, Laurito SR, Moraes CT, Mayorga L.   +6 more
europepmc   +1 more source

Screening of the mitochondrial A1555G mutation in patients with sensorineural hearing loss. [PDF]

Braz J Otorhinolaryngol, 2008
Maniglia LP, Moreira BCL, da Silva MAOM, Piatto VB, Maniglia JV.   +4 more
europepmc   +1 more source

Cancer cell growth and survival as a system-level property sustained by enhanced glycolysis and mitochondrial metabolic remodeling. [PDF]

Front Physiol, 2012
Alberghina L, Gaglio D, Gelfi C, Moresco RM, Mauri G, Bertolazzi P, Messa C, Gilardi MC, Chiaradonna F, Vanoni M.   +9 more
europepmc   +1 more source