about
Dysferlin mutations and mitochondrial dysfunctionRespiratory chain deficiency in aged spinal motor neurons.Comparison of mitochondrial mutation spectra in ageing human colonic epithelium and disease: absence of evidence for purifying selection in somatic mitochondrial DNA point mutations.Cutting edge genomics reveal new insights into tumour development, disease progression and therapeutic impacts in multiple myeloma.Accurate measurement of mitochondrial DNA deletion level and copy number differences in human skeletal muscle.Mitochondrial donation--how many women could benefit?A novel immunofluorescent assay to investigate oxidative phosphorylation deficiency in mitochondrial myopathy: understanding mechanisms and improving diagnosis.Extensive respiratory chain defects in inhibitory interneurones in patients with mitochondrial disease.Mitochondrial and inflammatory changes in sporadic inclusion body myositisInvestigating complex I deficiency in Purkinje cells and synapses in patients with mitochondrial diseaseUnique quadruple immunofluorescence assay demonstrates mitochondrial respiratory chain dysfunction in osteoblasts of aged and PolgA(-/-) miceSudden adult death syndrome in m.3243A>G-related mitochondrial disease: an unrecognized clinical entity in young, asymptomatic adultsMitochondrial dysfunction in myofibrillar myopathy.Disease progression in patients with single, large-scale mitochondrial DNA deletions.Pseudo-obstruction, stroke, and mitochondrial dysfunction: A lethal combination.Triplex real-time PCR--an improved method to detect a wide spectrum of mitochondrial DNA deletions in single cells.Spatial frequency bandwidth of surround suppression tuning curves.Age-dependent homeostatic plasticity of GABAergic signaling in developing retinal networks.Complex mitochondrial DNA rearrangements in individual cells from patients with sporadic inclusion body myositis.Pathological mechanisms underlying single large-scale mitochondrial DNA deletions.Translocation Breakpoints Preferentially Occur in Euchromatin and Acrocentric Chromosomes.Decreased male reproductive success in association with mitochondrial dysfunction.Simultaneous profiling of activity patterns in multiple neuronal subclasses.Phenotypic heterogeneity in m.3243A>G mitochondrial disease: The role of nuclear factors.Skeletal muscle mitochondrial oxidative phosphorylation function in idiopathic pulmonary arterial hypertension: in vivo and in vitro study.Mitochondrial dysfunction within the synapses of substantia nigra neurons in Parkinson's disease.mtDNA heteroplasmy level and copy number indicate disease burden in m.3243A>G mitochondrial disease.Subclonal evolution in disease progression from MGUS/SMM to multiple myeloma is characterised by clonal stabilityGraphical user interface for simultaneous profiling of activity patterns in multiple neuronal subclassesInherited pathogenic mitochondrial DNA mutations and gastrointestinal stem cell populationsGenomic stratification and liquid biopsy in a rare adrenocortical carcinoma (ACC) case, with dual lung metastases.Dissecting the neuronal vulnerability underpinning Alpers' syndrome: a clinical and neuropathological studyPTEN deletion drives acute myeloid leukemia resistance to MEK inhibitorsDevelopment and validation of a targeted gene sequencing panel for application to disparate cancersChromosome arm aneuploidies shape tumour evolution and drug response
P50
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P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
John Grady
@ast
John Grady
@en
John Grady
@es
John Grady
@nl
John Grady
@sl
type
label
John Grady
@ast
John Grady
@en
John Grady
@es
John Grady
@nl
John Grady
@sl
prefLabel
John Grady
@ast
John Grady
@en
John Grady
@es
John Grady
@nl
John Grady
@sl
P106
P1153
55259925800
P21
P31
P496
0000-0001-9667-3872