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Fructose-asparagine is a primary nutrient during growth of Salmonella in the inflamed intestineChIP-Seq and RNA-Seq reveal an AmrZ-mediated mechanism for cyclic di-GMP synthesis and biofilm development by Pseudomonas aeruginosaPhosphatidylinositol 3-kinase (PI3K) signaling via glycogen synthase kinase-3 (Gsk-3) regulates DNA methylation of imprinted lociPancreatic beta cells require NeuroD to achieve and maintain functional maturityAn international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge.Defining the role of pneumococcal neuraminidases and O-glycosidase in pneumococcal haemolytic uraemic syndrome.HrrF is the Fur-regulated small RNA in nontypeable Haemophilus influenzae.Intrauterine growth restriction is a direct consequence of localized maternal uropathogenic Escherichia coli cystitisUse of a targeted, combinatorial next-generation sequencing approach for the study of bicuspid aortic valve.Churchill: an ultra-fast, deterministic, highly scalable and balanced parallelization strategy for the discovery of human genetic variation in clinical and population-scale genomics.A genome-wide association study of congenital cardiovascular left-sided lesions shows association with a locus on chromosome 20.CREB-mediated alterations in the amygdala transcriptome: coordinated regulation of immune response genes following cocaine.Utilization of Whole Exome Sequencing to Identify Causative Mutations in Familial Congenital Heart Disease.Broad functional correction of molecular impairments by systemic delivery of scAAVrh74-hSGSH gene delivery in MPS IIIA mice.A Novel In Vitro Human Granuloma Model of Sarcoidosis and Latent TB Infection.Gene copy-number variations (CNVs) of complement C4 and C4A deficiency in genetic risk and pathogenesis of juvenile dermatomyositis.AR-13, a Celecoxib Derivative, Directly Kills Francisella In Vitro and Aids Clearance and Mouse Survival In Vivo.The nucleosome map of the mammalian liver.A patient with van Maldergem syndrome with endocrine abnormalities, hypogonadotropic hypogonadism, and breast aplasia/hypoplasia.Control of pancreatic β cell regeneration by glucose metabolism.Functional genomics of the beta-cell: short-chain 3-hydroxyacyl-coenzyme A dehydrogenase regulates insulin secretion independent of K+ currents.Safety Profile of Good Manufacturing Practice Manufactured Interferon γ-Primed Mesenchymal Stem/Stromal Cells for Clinical Trials.EF-P dependent pauses integrate proximal and distal signals during translation.Deletion of Pofut1 in Mouse Skeletal Myofibers Induces Muscle Aging-Related Phenotypes in cis and in trans.Blood genome-wide transcriptional profiles reflect broad molecular impairments and strong blood-brain links in Alzheimer's disease.Human CRMP4 mutation and disrupted Crmp4 expression in mice are associated with ASD characteristics and sexual dimorphism.A de novo nonsense mutation in ASXL3 shared by siblings with Bainbridge-Ropers syndrome.Genome sequencing identifies somatic BRAF duplication c.1794_1796dupTAC;p.Thr599dup in pediatric patient with low-grade ganglioglioma.Profiling the miRNome: Detecting Global miRNA Expression Levels with DNA MicroarraysGene Expression Analysis in Diabetes ResearchNutrition–hormone receptor–gene interactions: implications for development and diseasePathogenic variants in E3 ubiquitin ligase RLIM/RNF12 lead to a syndromic X-linked intellectual disability and behavior disorderIn-frame de novo mutation in in two patients with muscular atrophy and arthrogryposisWhole Transcriptome Analysis of Renal Intercalated Cells Predicts Lipopolysaccharide Mediated Inhibition of Retinoid X Receptor alpha FunctionPublisher Correction: Whole Transcriptome Analysis of Renal Intercalated Cells Predicts Lipopolysaccharide Mediated Inhibition of Retinoid X Receptor alpha FunctionReprioritization of biofilm metabolism is associated with nutrient adaptation and long-term survival of Haemophilus influenzaeSamovar: Single-Sample Mosaic Single-Nucleotide Variant Calling with Linked ReadsExpansion of B4GALT7 linkeropathy phenotype to include perinatal lethal skeletal dysplasiaExpanding the clinical history associated with syndromic Klippel-Feil: A unique case of comorbidity with medulloblastomaHuman Bile-Mediated Regulation of Salmonella Curli Fimbriae
P50
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P50
description
hulumtues
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researcher
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հետազոտող
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name
Peter White
@ast
Peter White
@en
Peter White
@es
Peter White
@nl
Peter White
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type
label
Peter White
@ast
Peter White
@en
Peter White
@es
Peter White
@nl
Peter White
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prefLabel
Peter White
@ast
Peter White
@en
Peter White
@es
Peter White
@nl
Peter White
@sl
P1053
E-4301-2011
P106
P21
P31
P3829
P496
0000-0002-5218-5903