Results 31 to 40 of about 199 (86)

Genetic Aspects for the Management of the Stocks of the Spiny Spider Crab Maja Brachydactyla: Heteroplasmy and Multipaternity [PDF]

, 2020
[Abstract] The spiny spider crab Maja brachydactyla is a decapod of high commercial interest. Despite the large number of studies conducted on this species, genetic research is still scarce. This doctoral thesis was focused on studying genetic aspects
Rodríguez Pena, Elba
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Dos familias con midd y melas: nivel de heteroplasmia de la mutación m.3243a>g y primer reporte de la mutación m.3271t>c en colombia

, 2016
MELAS syndrome (mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes) and MIDD syndrome (maternally inherited diabetes and deafness) are mitochondrial diseases caused in most cases by the same mutation m.3243A> G, which affects ...
Granadillo De Luque, Jorge Luis, Arteaga-Díaz, Juan Manuel, Hernández-Reina, Leonardo, Luna, Manuel, Arteaga-Diaz, Clara   +4 more
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Mutaciones en ARNt mitocondriales asociadas al síndrome de Leigh: estudio de la mutación m.5537Ti [PDF]

, 2020
El síndrome de Leigh es una enfermedad neurodegenerativa progresiva que suele aparecer en los primeros años de vida y es una de las enfermedades mitocondriales más comunes.
Emperador Ortiz, Sonia, Hernández Ainsa, Carmen, Martínez Cruz, Marina   +2 more
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Mitochondrial Oxidative Stress-A Causative Factor and Therapeutic Target in Many Diseases. [PDF]

Int J Mol Sci, 2021
Kowalczyk P, Sulejczak D, Kleczkowska P, Bukowska-Ośko I, Kucia M, Popiel M, Wietrak E, Kramkowski K, Wrzosek K, Kaczyńska K.   +9 more
europepmc   +1 more source

Mitochondrial DNA Polymorphism in HV1 and HV2 Regions and 12S rDNA in Perimenopausal Hypertensive Women. [PDF]

Biomedicines, 2023
Kwaśniewski W, Stupak A, Warowicka A, Goździcka-Józefiak A, Mosiewicz J, Mieczkowska J.   +5 more
europepmc   +1 more source

Mitochondrial Dysfunctions and Potential Molecular Markers in Sport Horses. [PDF]

Int J Mol Sci, 2022
Dzięgielewska A, Dunislawska A.
europepmc   +1 more source

Clinical, Genetic, and Histological Characterization of Patients with Rare Neuromuscular and Mitochondrial Diseases Presenting with Different Cardiomyopathy Phenotypes. [PDF]

Int J Mol Sci, 2023
Monda E, Lioncino M, Caiazza M, Simonelli V, Nesti C, Rubino M, Perna A, Mauriello A, Budillon A, Pota V, Bruno G, Varone A, Nigro V, Santorelli FM, Pacileo G, Russo MG, Frisso G, Sampaolo S, Limongelli G.   +18 more
europepmc   +1 more source

Mitochondrial DNA Changes in Respiratory Complex I Genes in Brain Gliomas. [PDF]

Biomedicines, 2023
Kozakiewicz P, Grzybowska-Szatkowska L, Ciesielka M, Całka P, Osuchowski J, Szmygin P, Jarosz B, Ostrowska-Leśko M, Dudka J, Tkaczyk-Wlizło A, Ślaska B.   +10 more
europepmc   +1 more source

HV1 and HV2 analysis of mitochondrial DNA from a sample of individuals from the City of São Paulo. Forensic aspects and study of heteroplasmy

, 2011
Em amostras biologicas em que a quantidade de DNA e muito pequena ou muito degradada ha uma maior probabilidade de se obter um perfil de DNA mitocondrial.Objetivos: Analisar os haplotipos mais frequentes em uma amostra da populacao da Cidade de São Paulo
Godoy, Carla Daniele de [UNIFESP]
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A phylogeny analysis on six mullet species (Teleosti: Mugillidae) using PCR-sequencing method [PDF]

, 2013
In this study, genetic differences and phylogenic relationships among six Mugillidae species (Mugil cephalus, M. capito, Liza subviridis, L. saliens, L. aurata, Valamugil buchanani) were determined using PCR-sequencing. M. cephalus, L. subviridis, and V.
Nematzadeh, M., Fahim, A., Khalesi, M.K., Laloei, F., Rezvani, S.   +4 more
core   +1 more source