Search Results - "Justin P Rubio"
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1
An 18-kDa Translocator Protein (TSPO) polymorphism explains differences in binding affinity of the PET radioligand PBR28
Published in Journal of cerebral blood flow and metabolism (01-01-2012)“…[11C]PBR28 binds the 18-kDa Translocator Protein (TSPO) and is used in positron emission tomography (PET) to detect microglial activation. However,…”
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2
Histamine Receptor 3 negatively regulates oligodendrocyte differentiation and remyelination
Published in PloS one (18-12-2017)“…Agents promoting oligodendrocyte precursor cell differentiation have the potential to restore halted and/or delayed remyelination in patients with multiple…”
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3
SIRT1 Activates MAO-A in the Brain to Mediate Anxiety and Exploratory Drive
Published in Cell (23-12-2011)“…SIRT1 is a NAD +-dependent deacetylase that governs a number of genetic programs to cope with changes in the nutritional status of cells and organisms…”
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4
Transcriptomic effects of rs4845604, an IBD and allergy-associated RORC variant, in stimulated ex vivo CD4+ T cells
Published in PloS one (21-10-2021)“…RORγt is an isoform of RORC, preferentially expressed in Th17 cells, that functions as a critical regulator of type 3 immunity. As murine Th17-driven…”
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5
Splicing, cis genetic variation and disease
Published in Biochemical Society transactions (01-12-2009)“…Splicing is a post-transcriptional modification of RNA during which introns are removed and exons are joined. Most of the mammalian genes undergo constitutive…”
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6
A conserved sorting-associated protein is mutant in chorea-acanthocytosis
Published in Nature genetics (01-06-2001)“…Chorea-acanthocytosis (CHAC, MIM 200150) is an autosomal recessive neurodegenerative disorder characterized by the gradual onset of hyperkinetic movements and…”
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7
McLeod neuroacanthocytosis: Genotype and phenotype
Published in Annals of neurology (01-12-2001)“…McLeod syndrome is caused by mutations of XK, an X‐chromosomal gene of unknown function. Originally defined as a peculiar Kell blood group variant, the disease…”
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8
Background and Breakthrough Opioid Choice May Determine Different Pain Outcomes
Published in Journal of pain and symptom management (01-03-2024)Get full text
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9
Opioid Switch Dosing in Chronic Cancer Pain: A Prospective Longitudinal Study
Published in Journal of palliative medicine (01-03-2024)“…Opioid switching is common, however, conversion tables have limitations. Guidelines suggest postswitch dose reduction, yet, observations show opioid doses may…”
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10
Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci
Published in Annals of neurology (01-12-2011)“…Objective: To perform a 1‐stage meta‐analysis of genome‐wide association studies (GWAS) of multiple sclerosis (MS) susceptibility and to explore functional…”
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11
Evidence for the role of FMR1 gray zone alleles as a risk factor for parkinsonism in females
Published in Movement disorders (01-07-2018)“…ABSTRACT Background and Objective There is convincing evidence that small CGG expansion (41‐54 repeats): FMR1 “gray zone” alleles (GZ) contribute to the risk…”
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12
Variants of ST8SIA1 are associated with risk of developing multiple sclerosis
Published in PloS one (09-07-2008)“…Multiple sclerosis (MS) is an inflammatory demyelinating disease of the central nervous system of unknown etiology with both genetic and environmental factors…”
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13
Tafenoquine treatment of Plasmodium vivax malaria: suggestive evidence that CYP2D6 reduced metabolism is not associated with relapse in the Phase 2b DETECTIVE trial
Published in Malaria journal (18-02-2016)“…Tafenoquine (TQ) and primaquine (PQ) are 8-aminoquinolines (8-AQ) with anti-hypnozoite activity against vivax malaria. PQ is the only FDA-approved medicine for…”
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14
Estimation of the Antirelapse Efficacy of Tafenoquine, Using Plasmodium vivax Genotyping
Published in The Journal of infectious diseases (01-03-2016)“…Prevention of relapse of Plasmodium vivax infection is a key treatment goal in malaria. Use of P. vivax genotyping in a multicenter, double-blind, randomized,…”
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15
Genetic deficiency of plasma lipoprotein-associated phospholipase A2 (PLA2G7 V297F null mutation) and risk of Alzheimer's disease in Japan
Published in Journal of Alzheimer's disease (02-09-2010)“…High plasma lipoprotein phospholipase A2 activity (Lp-PLA2) is reported to be a risk factor for dementia. A loss of function polymorphism in the Lp-PLA2 gene -…”
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16
Transcriptomic effects of rs4845604, an IBD and allergy-associated RORC variant, in stimulated ex vivo CD4+ T cells
Published in PloS one (21-10-2021)“…RORγt is an isoform of RORC, preferentially expressed in Th17 cells, that functions as a critical regulator of type 3 immunity. As murine Th17-driven…”
Get full text
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17
Evaluation of the effect of UGT1A1 polymorphisms on dolutegravir pharmacokinetics
Published in Pharmacogenomics (01-01-2014)“…To evaluate potential pharmacogenetic effects of UGT1A1 polymorphisms on the pharmacokinetics (PK) of dolutegravir (Tivicay®; ViiV Healthcare, NC, USA), an…”
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18
Exome array analysis suggests an increased variant burden in families with schizophrenia
Published in Schizophrenia research (01-07-2017)“…Abstract The exome array assays rare-but-recurrent, likely deleterious, exonic variants and represents an intermediary between single nucleotide polymorphism…”
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19
Effects of enzyme inducers efavirenz and tipranavir/ritonavir on the pharmacokinetics of the HIV integrase inhibitor dolutegravir
Published in European journal of clinical pharmacology (01-10-2014)“…Purpose Dolutegravir (DTG) is an unboosted, integrase inhibitor for the treatment of HIV infection. Two studies evaluated the effects of efavirenz (EFV) and…”
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20
Saliva-Derived DNA Performs Well in Large-Scale, High-Density Single-Nucleotide Polymorphism Microarray Studies
Published in Cancer epidemiology, biomarkers & prevention (01-03-2010)“…As of June 2009, 361 genome-wide association studies (GWAS) had been referenced by the HuGE database. GWAS require DNA from many thousands of individuals,…”
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