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Organizing biological data
Pasteurella multocida from deep nasal swabs and tracheobronchial lavage in calves
Homo sapiens
Novel Biallelic NARS2 Variants Leading To Refractory Seizures: A Case Report And Literature Review
FabT_+or-Tween_S.pyogenesM28_Transcriptomic analysis
Interaction between RA/JIA-associated PTPN2 loss of function and patient microbiome promotes the gut-joint axis in mice
Allogenomics
Identification of predictive models including polymorphisms in cytokines genes and clinical variables associated with post-transplant complications after identical HLA-allogeneic stem cell transplantation
Human skeletal muscle possesses an epigenetic memory of high intensity interval training
Plasmodium falciparum
Plasmodium falciparum selective whole genome amplification (sWGA)
The RNAseq analysis covered both the long- and short-winged variants of Nilaparvata lugens, along with Pyrrhocoris apterus
Paradendryphiella salina
Paradendryphiella salina Genome sequencing
Peninsula Iberica deep aquifers
Peninsula Iberica deep aquifers Metagenome
Changes of the gut microbiota and metabolite characteristics in obesity-prone and obesity-resistant dogs induced by a high-fat diet
A reference genome of Commelinales provides insights into the commelinids evolution and global spread of water hyacinth ( Pontederia crassipes)
FSGS
The most common founder pathogenic variant c.868G>A (p.Val290Met) in the NPHS2 gene in a representative ADULT Czech cohort with Focal Segmental Glomerulosclerosis (FSGS) is associated with a milder disease and its underdiagnosis in childhood.
Defence heterogeneity in host populations gives rise to pathogen diversity
Linear epitope mapping in the E and NS1 proteins of dengue and Zika viruses: prospection of peptides for vaccines and diagnostics GA_DZ_V2
Effects of chemical in vitro activation versus fragmentation on human ovarian tissue and follicle growth in culture
Mutation in mitochondrial chaperone TRAP1 is responsible for male-specific autism
The impact of Mmu17 non-Hsa21 orthologous genes in the Ts65Dn mouse model of Down syndrome: the “gold standard” refuted
DADA2TWINS
Consistent disease manifestations with a staggered time course in two identical twins affected by adenosine deaminase 2 deficiency
Altered DNA Methylation and Gene expression predict Disease Severity in Patients with Aicardi-Goutières Syndrome
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