نتایج جستجو برای: mitochondrial encephalomyopathy

تعداد نتایج: 132426  

Journal: :Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease 1995

2011
Emiliano González-Vioque Javier Torres-Torronteras Antoni L. Andreu Ramon Martí

Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE) is a severe human disease caused by mutations in TYMP, the gene encoding thymidine phosphorylase (TP). It belongs to a broader group of disorders characterized by a pronounced reduction in mitochondrial DNA (mtDNA) copy number in one or more tissues. In most cases, these disorders are caused by mutations in genes involved in deoxyrib...

2014
Taraka R. Donti Carmen Stromberger Ming Ge Karen W. Eldin William J. Craigen Brett H. Graham

Mutations in subunits of succinyl-CoA synthetase/ligase (SCS), a component of the citric acid cycle, are associated with mitochondrial encephalomyopathy, elevation of methylmalonic acid (MMA), and mitochondrial DNA (mtDNA) depletion. A FACS-based retroviral-mediated gene trap mutagenesis screen in mouse embryonic stem (ES) cells for abnormal mitochondrial phenotypes identified a gene trap allel...

Journal: :Stroke 2001
E Martínez-Fernández A Gil-Peralta R García-Lozano I Chinchón I Aguilera O Fernández-López J Arenas Y Campos J Bautista

BACKGROUND AND PURPOSE It is well known that some mitochondrial disorders are responsible for ischemic cerebral infarction in young patients. Our purpose was to determine, in this prospective ongoing study, whether ischemic stroke is the only manifestation of a mitochondrial disorder in young patients. METHODS Patients aged </=50 years, admitted to the Stroke Unit from January 1999 to May 200...

Journal: :The Journal of biological chemistry 2007
Matthew McKenzie Danae Liolitsa Natalya Akinshina Michelangelo Campanella Sanjay Sisodiya Ian Hargreaves Niranjanan Nirmalananthan Mary G Sweeney Patrick M Abou-Sleiman Nicholas W Wood Michael G Hanna Michael R Duchen

Mitochondrial encephalomyopathy and lactic acidosis with strokelike episodes (MELAS) is a severe young onset stroke disorder without effective treatment. We have identified a MELAS patient harboring a 13528A-->G mitochondrial DNA (mtDNA) mutation in the Complex I ND5 gene. This mutation was homoplasmic in mtDNA from patient muscle and nearly homoplasmic (99.9%) in blood. Fibroblasts from the pa...

2013
John Hayman

Charles Darwin's long-term illness has been the subject of much speculation. His numerous symptoms have led to conclusions that his illness was essentially psychogenic in nature. These diagnoses have never been fully convincing, however, particularly in regard to the proposed underlying psychological background causes of the illness. Similarly, two proposed somatic causes of illness, Chagas dis...

2018
Francesco Bruni Ivano Di Meo Emanuele Bellacchio Bryn D Webb Robert McFarland Zofia M A Chrzanowska-Lightowlers Langping He Ewa Skorupa Isabella Moroni Anna Ardissone Anna Walczak Henna Tyynismaa Pirjo Isohanni Hanna Mandel Holger Prokisch Tobias Haack Penelope E Bonnen Bertini Enrico Ewa Pronicka Daniele Ghezzi Robert W Taylor Daria Diodato

In recent years, an increasing number of mitochondrial disorders have been associated with mutations in mitochondrial aminoacyl-tRNA synthetases (mt-aaRSs), which are key enzymes of mitochondrial protein synthesis. Bi-allelic functional variants in VARS2, encoding the mitochondrial valyl tRNA-synthetase, were first reported in a patient with psychomotor delay and epilepsia partialis continua as...

Journal: :Human molecular genetics 2013
Laura García-Corzo Marta Luna-Sánchez Carolina Doerrier José A García Adela Guarás Rebeca Acín-Pérez Javier Bullejos-Peregrín Ana López Germaine Escames José A Enríquez Darío Acuña-Castroviejo Luis C López

Coenzyme Q10 (CoQ(10)) or ubiquinone is a well-known component of the mitochondrial respiratory chain. In humans, CoQ(10) deficiency causes a mitochondrial syndrome with an unexplained variability in the clinical presentations. To try to understand this heterogeneity in the clinical phenotypes, we have generated a Coq9 Knockin (R239X) mouse model. The lack of a functional Coq9 protein in homozy...

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