Search Results - "PAGE, Grier P"
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1
MEK inhibition exhibits efficacy in human and mouse neurofibromatosis tumors
Published in The Journal of clinical investigation (01-01-2013)“…Neurofibromatosis type 1 (NF1) patients develop benign neurofibromas and malignant peripheral nerve sheath tumors (MPNST). These incurable peripheral nerve…”
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2
Late-Onset Sepsis in Very Low Birth Weight Infants from Singleton and Multiple-Gestation Births
Published in The Journal of pediatrics (01-06-2013)“…Objectives To describe and compare the incidence of late-onset sepsis (LOS) and demographic and clinical characteristics associated with LOS in very low birth…”
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3
The interactome of the N-terminus of band 3 regulates red blood cell metabolism and storage quality
Published in Haematologica (Roma) (01-11-2021)“…Band 3 (anion exchanger 1; AE1) is the most abundant membrane protein in red blood cells, which in turn are the most abundant cells in the human body. A…”
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4
FLOWERING LOCUS T duplication coordinates reproductive and vegetative growth in perennial poplar
Published in Proceedings of the National Academy of Sciences - PNAS (28-06-2011)“…Annual plants grow vegetatively at early developmental stages and then transition to the reproductive stage, followed by senescence in the same year. In…”
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5
Comparison of maternal venous blood metabolomics collected as dried blood spots, dried blood microsamplers, and plasma for integrative environmental health research
Published in Environment international (01-05-2024)“…[Display omitted] •309 maternal metabolites in dried blood microsamplers (DBM) and spots (DBS), and plasma.•Moderate metabolite correlation and rank level…”
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6
Sex-specific genetic modifiers identified susceptibility of cold stored red blood cells to osmotic hemolysis
Published in BMC genomics (23-03-2022)“…Genetic variants have been found to influence red blood cell (RBC) susceptibility to hemolytic stress and affect transfusion outcomes and the severity of blood…”
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7
Identification of genes required for cellulose synthesis by regression analysis of public microarray data sets
Published in Proceedings of the National Academy of Sciences - PNAS (14-06-2005)“…Coexpression patterns of gene expression across many microarray data sets may reveal networks of genes involved in linked processes. To identify factors…”
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8
Integrated Genomic Analyses in Bronchopulmonary Dysplasia
Published in The Journal of pediatrics (01-03-2015)“…Objective To identify single-nucleotide polymorphisms (SNPs) and pathways associated with bronchopulmonary dysplasia (BPD) because O2 requirement at 36 weeks'…”
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9
Familial and Genetic Susceptibility to Major Neonatal Morbidities in Preterm Twins
Published in Pediatrics (Evanston) (01-06-2006)“…Intraventricular hemorrhage, necrotizing enterocolitis, and bronchopulmonary dysplasia remain significant causes of morbidity and mortality in preterm…”
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10
Ethnicity, sex, and age are determinants of red blood cell storage and stress hemolysis: results of the REDS-III RBC-Omics study
Published in Blood advances (27-06-2017)“…Genetic polymorphisms in blood donors may contribute to donor-specific differences in the survival of red blood cells (RBCs) during cold storage and after…”
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11
Transcriptional Coordination of the Metabolic Network in Arabidopsis
Published in Plant physiology (Bethesda) (01-10-2006)“…Patterns of coexpression can reveal networks of functionally related genes and provide deeper understanding of processes requiring multiple gene products. We…”
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12
Brief Report: Hydroxychloroquine does not induce hemolytic anemia or organ damage in a “humanized” G6PD A- mouse model
Published in PloS one (02-10-2020)“…Background Hydroxychloroquine (HCQ) is widely used in the treatment of malaria, rheumatologic disease such as lupus, and most recently, COVID-19. These uses…”
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13
CressExpress: A Tool For Large-Scale Mining of Expression Data from Arabidopsis
Published in Plant physiology (Bethesda) (01-07-2008)“…CressExpress is a user-friendly, online, coexpression analysis tool for Arabidopsis (Arabidopsis thaliana) microarray expression data that computes patterns of…”
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14
Urinary Peptidome May Predict Renal Function Decline in Type 1 Diabetes and Microalbuminuria
Published in Journal of the American Society of Nephrology (01-09-2009)“…One third of patients with type 1 diabetes and microalbuminuria experience an early, progressive decline in renal function that leads to advanced stages of…”
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15
Large genome-wide association study identifies three novel risk variants for restless legs syndrome
Published in Communications biology (25-11-2020)“…Restless legs syndrome (RLS) is a common neurological sensorimotor disorder often described as an unpleasant sensation associated with an urge to move the…”
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16
Donor genetic and nongenetic factors affecting red blood cell transfusion effectiveness
Published in JCI insight (11-01-2022)“…BACKGROUNDRBC transfusion effectiveness varies due to donor, component, and recipient factors. Prior studies identified characteristics associated with…”
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17
Gene expression profiling of aging in multiple mouse strains: identification of aging biomarkers and impact of dietary antioxidants
Published in Aging cell (01-08-2009)“…Summary We used DNA microarrays to identify panels of transcriptional markers of aging that are differentially expressed in young (5 month) and old (25 month)…”
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18
Genetic Contributions to Urgency Urinary Incontinence in Women
Published in The Journal of urology (01-06-2015)“…Purpose We identify genetic variants associated with urgency urinary incontinence in postmenopausal women. Materials and Methods A 2-stage genome-wide…”
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19
Evaluation of pediatric epigenetic clocks across multiple tissues
Published in Clinical epigenetics (02-09-2023)“…Epigenetic clocks are promising tools for assessing biological age. We assessed the accuracy of pediatric epigenetic clocks in gestational and chronological…”
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20
DCDC2 Is Associated with Reading Disability and Modulates Neuronal Development in the Brain
Published in Proceedings of the National Academy of Sciences - PNAS (22-11-2005)“…DYX2 on 6p22 is the most replicated reading disability (RD) locus. By saturating a previously identified peak of association with single nucleotide…”
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