about
Mitochondrial DNA damage patterns and aging: revising the evidences for humans and miceMitochondrial DNA and Y-chromosome structure at the mediterranean and atlantic façades of the iberian peninsulaNuclear insertions of mitochondrial origin: Database updating and usefulness in cancer studiesMitochondrial DNA patterns in the Iberian Northern plateau: population dynamics and substructure of the Zamora province.Frequency and pattern of heteroplasmy in the control region of human mitochondrial DNA.Familial hypercholesterolemia: Molecular characterization of possible cases from the Azores Islands (Portugal).Frequency and pattern of heteroplasmy in the complete human mitochondrial genome.Validated primer set that prevents nuclear DNA sequences of mitochondrial origin co-amplification: a revision based on the New Human Genome Reference Sequence (GRCh37).Linguistic isolates in Portugal: insights from the mitochondrial DNA pattern.Novel candidate blood-based transcriptional biomarkers of Machado-Joseph disease.Involvement of mitochondrial haplogroups in myocardial infarction and stroke: A case-control study in Castile and Leon (Spain) population.Promoter Variant Alters Expression of the Autophagic BECN1 Gene: Implications for Clinical Manifestations of Machado-Joseph Disease.Differential mtDNA damage patterns in a transgenic mouse model of Machado-Joseph disease (MJD/SCA3).Verification of Inter-laboratorial Genotyping Consistency in the Molecular Diagnosis of Polyglutamine Spinocerebellar Ataxias.Triplet Repeat Primed PCR (TP-PCR) in Molecular Diagnostic Testing for Spinocerebellar Ataxia Type 3 (SCA3).Primer effect in the detection of mitochondrial DNA point heteroplasmy by automated sequencing.Replicating studies of genetic modifiers in spinocerebellar ataxia type 3: can homogeneous cohorts aid?Mitochondrial DNA haplogroups and age at onset of Machado-Joseph disease/Spinocerebellar ataxia type 3: a study in patients from multiple populationsPromoter Variation and Expression Levels of Inflammatory Genes IL1A, IL1B, IL6 and TNF in Blood of Spinocerebellar Ataxia Type 3 (SCA3) PatientsThe role of control region mitochondrial DNA mutations in cardiovascular disease: stroke and myocardial infarction
P50
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P50
description
hulumtuese
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Amanda Ramos
@ast
Amanda Ramos
@en
Amanda Ramos
@es
Amanda Ramos
@nl
Amanda Ramos
@sl
type
label
Amanda Ramos
@ast
Amanda Ramos
@en
Amanda Ramos
@es
Amanda Ramos
@nl
Amanda Ramos
@sl
prefLabel
Amanda Ramos
@ast
Amanda Ramos
@en
Amanda Ramos
@es
Amanda Ramos
@nl
Amanda Ramos
@sl
P1053
K-3739-2014
P106
P1153
24462249400
P21
P31
P3829
P496
0000-0002-9806-6651
P569
2000-01-01T00:00:00Z