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The genome of the obligate intracellular parasite Trachipleistophora hominis: new insights into microsporidian genome dynamics and reductive evolutionMetaBase--the wiki-database of biological databasesPEX6 is Expressed in Photoreceptor Cilia and Mutated in Deafblindness with Enamel Dysplasia and MicrocephalyInduction of the mammalian node requires Arkadia function in the extraembryonic lineagesEarly-onset lymphoproliferation and autoimmunity caused by germline STAT3 gain-of-function mutationsThe EIF2AK3 gene region and type I diabetes in subjects from South IndiaThe molecular phenotype of heparan sulfate in the Hs2st-/- mutant mouseCrowdsourced direct-to-consumer genomic analysis of a family quartetLow budget analysis of Direct-To-Consumer genomic testing familial dataAn approach to describing and analysing bulk biological annotation quality: a case study using UniProtKBDNA methylation patterns in cord blood DNA and body size in childhoodMutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair SyndromeBioStar: An Online Question & Answer Resource for the Bioinformatics CommunityStrand selective generation of endo-siRNAs from the Na/phosphate transporter gene Slc34a1 in murine tissuesImproving and correcting the contiguity of long-read genome assemblies of three plant species using optical mapping and chromosome conformation capture data.Python for information theoretic analysis of neural dataSkeletal site-related variation in human trabecular bone transcriptome and signalingBioinformatic selection of putative epigenetically regulated loci associated with obesity using gene expression data.A mutation in the 5'-UTR of IFITM5 creates an in-frame start codon and causes autosomal-dominant osteogenesis imperfecta type V with hyperplastic callus.Postnatal growth and DNA methylation are associated with differential gene expression of the TACSTD2 gene and childhood fat mass.A CD4 T cell gene signature for early rheumatoid arthritis implicates interleukin 6-mediated STAT3 signalling, particularly in anti-citrullinated peptide antibody-negative disease.A germline mutation of CDKN2A and a novel RPLP1-C19MC fusion detected in a rare melanotic neuroectodermal tumor of infancy: a case report.Emergence of wheat blast in Bangladesh was caused by a South American lineage of Magnaporthe oryzae.Effects of Sirt1 on DNA methylation and expression of genes affected by dietary restriction.What do natural antisense transcripts regulate?Autosomal dominant SCA5 and autosomal recessive infantile SCA are allelic conditions resulting from SPTBN2 mutations.The supposed tumor suppressor gene WWOX is mutated in an early lethal microcephaly syndrome with epilepsy, growth retardation and retinal degeneration.What are natural antisense transcripts good for?Analysis of differential gene-regulatory responses to zinc in human intestinal and placental cell lines.Selenium alters miRNA profile in an intestinal cell line: evidence that miR-185 regulates expression of GPX2 and SEPSH2.Glutathione peroxidase 4 has a major role in protecting mitochondria from oxidative damage and maintaining oxidative phosphorylation complexes in gut epithelial cells.Immediate and gradual gene expression changes in telomerase over-expressing fibroblasts.Association of mutations in the NALP3/CIAS1/PYPAF1 gene with a broad phenotype including recurrent fever, cold sensitivity, sensorineural deafness, and AA amyloidosis.A genome wide analysis of the response to uncapped telomeres in budding yeast reveals a novel role for the NAD+ biosynthetic gene BNA2 in chromosome end protection.Leaf LIMS: A Flexible Laboratory Information Management System with a Synthetic Biology Focus.A role for the pregnane X receptor in flucloxacillin-induced liver injury.A variation in the ghrelin gene increases weight and decreases insulin secretion in tall, obese children.Pattern recognition receptor expression is not impaired in patients with chronic mucocutanous candidiasis with or without autoimmune polyendocrinopathy candidiasis ectodermal dystrophy.Comparative gene expression profiling of human umbilical vein endothelial cells and ocular vascular endothelial cells.Identification of the pathogenic pathways in osteoarthritic hip cartilage: commonality and discord between hip and knee OA
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description
hulumtues
@sq
onderzoeker
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researcher
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հետազոտող
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name
Daniel C Swan
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Daniel C Swan
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Daniel C Swan
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Daniel C Swan
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Daniel C Swan
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Daniel C Swan
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Daniel C Swan
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Daniel C Swan
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Daniel C Swan
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Daniel C Swan
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D Swan
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DC Swan
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Dan Swan
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Daniel C. Swan
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Daniel Swan
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Daniel C Swan
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Daniel C Swan
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Daniel C Swan
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Daniel C Swan
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Daniel C Swan
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P108
P106
P108
P1153
14044115000
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daniel-swan
P496
0000-0001-8978-8129