Results 221 to 230 of about 73,771 (300)

Neurological diagnoses in children potentially fulfilling the criteria for developmental coordination disorder

open access: yesDevelopmental Medicine &Child Neurology, EarlyView.
In children potentially fulfilling the criteria for developmental coordination disorder (DCD), phenotypical assessment does not sufficiently predict the diagnostic outcome (i.e. DCD or an alternative diagnosis). Due to the lack of distinguishing clinical and diagnostic features and the high prevalence of genetic diagnoses in these patients, additional ...
Martinica Garofalo   +5 more
wiley   +1 more source

Disentangling the relationship between glucose, insulin and brain health: A UK Biobank study

open access: yesDiabetes, Obesity and Metabolism, EarlyView.
Abstract Background Glycaemic traits are associated with poorer brain health and dementia risk. Recent advances in genetic instruments for specific glycaemic markers enable an in‐depth investigation of the likely nature of associations and underlying mechanisms between diabetes‐related mechanisms and brain health and dementia.
Andrew C. Mason   +7 more
wiley   +1 more source

QTL Mapping of Yield-Related Traits in Tetraploid Wheat Based on Wheat55K SNP Array. [PDF]

open access: yesPlants (Basel)
Jia Y   +11 more
europepmc   +1 more source

Genetic risk factor identification for common epilepsies guided by integrative omics data analysis

open access: yesEpilepsia, EarlyView.
Abstract Objective Genetic generalized epilepsies (GGEs) comprise the most common genetically determined epilepsy syndromes, following a complex mode of inheritance. Although many important common and rare genetic factors causing or contributing to these epilepsies have been identified in the past decades, many features of the genetic architecture are ...
Ashwini Mushunuri   +9 more
wiley   +1 more source

Evaluating Translocation Gene Fusions by SNP Array Data

open access: yesCancer Informatics, 2011
Hong Liu   +6 more
doaj  

Mapping of Aegilops speltoides derived leaf rust and stripe rust resistance genes using 35K SNP array. [PDF]

open access: yesBMC Genom Data
Kaur B   +7 more
europepmc   +1 more source

Comprehensive high-resolution genomic profiling and cytogenetics of human chondrocyte cultures by GTG-banding, locus-specific FISH, SKY and SNP array

open access: gold, 2018
Marco Wallenborn   +11 more
openalex   +1 more source

Conditional deletion of the multiple sclerosis susceptibility gene ATXN1 identifies cell‐autonomous effects in the B‐cell compartment

open access: yesThe FEBS Journal, EarlyView.
Ataxin‐1 is a polyglutamine protein associated with the etiology of spinocerebellar ataxia type 1 (SCA1) that has been recently found implicated in the risk of developing the autoimmune disorder multiple sclerosis (MS). Here, we took a conditional knockout approach to ablate ataxin‐1 exclusively in the B‐cell compartment and we found that this protein ...
Jonathan Jacob Carver   +3 more
wiley   +1 more source

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