Results 271 to 280 of about 290,368 (328)

Deletion of the HLA-B Gene in One of the Inherited Haplotypes in a Northern European Family. [PDF]

open access: yesHLA
Grünebach F   +8 more
europepmc   +1 more source

Type 1 diabetes risk factors, risk prediction and presymptomatic detection: Evidence and guidance for screening

open access: yesDiabetes, Obesity and Metabolism, EarlyView.
Abstract Type 1 diabetes is recognized as a chronic disease with a presymptomatic phase that does not require insulin therapy and a clinical phase where insulin treatment becomes necessary. The presymptomatic phase is characterized by the presence of autoantibodies targeting pancreatic islet beta cell antigens (islet autoantibodies).
Ezio Bonifacio   +1 more
wiley   +1 more source

Type 1 Diabetes: A Guide to Autoimmune Mechanisms for Clinicians

open access: yesDiabetes, Obesity and Metabolism, EarlyView.
Abstract Type 1 diabetes (T1D) results from the destruction of pancreatic beta cells by autoreactive T lymphocytes, leading to insulin deficiency and lifelong insulin dependence. It develops in genetically predisposed individuals, triggered by environmental or immunological factors.
François‐Xavier Mauvais   +1 more
wiley   +1 more source

Novel Shared Heritable Candidate Risk Loci of Breast and Endometrial Cancer-A Swedish Haplotype Genome-Wide Association Study. [PDF]

open access: yesInt J Mol Sci
Barnekow E   +10 more
europepmc   +1 more source

Invasive insect genetics: Start codon targeted (SCoT) markers provide superior data to describe genetic diversity of brown marmorated stink bug, Halyomorpha halys, in a newly colonized region

open access: yesEntomologia Experimentalis et Applicata, EarlyView.
In this study, we assessed the genetic diversity of Halyomorpha halys, an invasive agricultural pest, in Türkiye using start codon targeted (SCoT) markers and mitochondrial cytochrome c oxidase subunit I (COI) sequences. SCoT markers revealed high polymorphism (91.4%) and six genetic clusters among 71 specimens from 12 provinces, with Trabzon showing ...
Ismail Oguz Ozdemir   +5 more
wiley   +1 more source

Cell type mapping of mild malformations of cortical development with oligodendroglial hyperplasia in epilepsy using single‐nucleus multiomics

open access: yesEpilepsia, EarlyView.
Abstract Objective Mild malformations of cortical development with oligodendroglial hyperplasia in epilepsy (MOGHE) are brain lesions associated with focal epilepsy and characterized by increased oligodendroglial density, heterotopic neurons, and hypomyelination in the white matter.
Isabella C. Galvão   +10 more
wiley   +1 more source

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