Résultats de la recherche

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Genetics, genomics, and evolutionary biology of NKG2D ligands.
Use of in vivo imaging to monitor the progression of experimental mouse cytomegalovirus infection in neonates.
Next-Generation Sequencing of the HLA locus: Methods and impacts on HLA typing, population genetics and disease association studies.
The TRANSPLANTEX initiative.
Back to the future: bacteriophages as promising therapeutic tools.
Natural Killer Group 2, Member D/NKG2D Ligands in Hematopoietic Cell Transplantation.
The non-conventional MHC class I MR1 molecule controls infection by Klebsiella pneumoniae in mice.
Increased Viral Dissemination in the Brain and Lethality in MCMV-Infected, Dicer-Deficient Neonates
Cascade: a R package to study, predict and simulate the diffusion of a signal through a temporal gene network.
The miR-17 ∼ 92 Cluster: A Key Player in the Control of Inflammation during Rheumatoid Arthritis.
Eosinophilic myositis as first manifestation in a patient with type 2 myotonic dystrophy CCTG expansion mutation and rheumatoid arthritis.
B lymphocytes and B-cell activating factor promote collagen and profibrotic markers expression by dermal fibroblasts in systemic sclerosis.
Deregulation of Type I IFN-Dependent Genes Correlates with Increased Susceptibility to Cytomegalovirus Acute Infection of Dicer Mutant Mice.
Exome sequencing identifies a novel missense variant in CTSC causing nonsyndromic aggressive periodontitis.
Homozygosity for the V377I mutation in mevalonate kinase causes distinct clinical phenotypes in two sibs with hyperimmunoglobulinaemia D and periodic fever syndrome (HIDS).
Protein-altering MYH3 variants are associated with a spectrum of phenotypes extending to spondylocarpotarsal synostosis syndrome.
Homozygous IL36RN mutation and NSD1 duplication in a patient with severe pustular psoriasis and symptoms unrelated to deficiency of interleukin-36 receptor antagonist.
Reverse-engineering the genetic circuitry of a cancer cell with predicted intervention in chronic lymphocytic leukemia.

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