Results 161 to 170 of about 4,127,534 (292)
RNA Sequencing Resolves Cryptic Pathogenic Variants in Mitochondrial Disease
ABSTRACT Objective Mitochondrial diseases are the most common inherited metabolic disorders, characterized by pronounced clinical and genetic heterogeneity that complicates molecular diagnosis. Although DNA‐based sequencing approaches have become standard in genetic testing, up to half of patients remain without a definitive diagnosis.
Zhimei Liu +21 more
wiley +1 more source
IMPACT OF FLUORESCENT DYES ON MUTATIONS IN NEXT GENERATION SEQUENCING LIBRARY GENERATION. [PDF]
Butty V, Patel P, Green S, Levine S.
europepmc +1 more source
IMLS Support to Idaho Libraries, 2014
Idaho Commission for Libraries report on finding to Idaho libraries from the Institute of Museum and Library Services for ...
Libraries, Idaho Commission for;
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ABSTRACT Background and Purpose White matter hyperintensities (WMH) are a core neuroimaging marker of cerebral small vessel disease (CSVD). Sleep apnoea (SA) is a recognized vascular risk factor, but its associations with regional WMH burden, short‐interval WMH change and cognitive performance in population‐based cohorts remain incompletely defined. We
Peng Cheng +4 more
wiley +1 more source
IMLS Support to Idaho Libraries, 2015
Idaho Commission for Libraries report on finding to Idaho libraries from the Institute of Museum and Library Services for ...
Libraries, Idaho Commission for;
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Association Between Motor Pathway Damage and Motor Deficit in Upper and Lower Limb in People With MS
ABSTRACT Objective Corticospinal tract damage is common in people with MS, but the degree of clinical symptoms varies. We hypothesize that corticospinal tract lesions are more extensive and severe in people with MS with motor impairments in both upper and lower limbs.
Mathilde Liffran +13 more
wiley +1 more source
A Perspective on Covalent Hit Identification and Validation in the European Pharmaceutical Industry. [PDF]
Schadt O, Essig S, Testolin G.
europepmc +1 more source
ABSTRACT Objective Variants in SLC6A1, encoding the GABA transporter 1 (GAT‐1), cause epilepsy, autism spectrum disorder, and developmental delay via loss of GABA uptake, impaired trafficking, and ER retention. We previously found that 4‐Phenylbutyrate (PBA), an FDA‐approved drug, restores GABA uptake and reduces seizures in SLC6A1‐related disorders ...
Melissa B. DeLeeuw +5 more
wiley +1 more source
Libraries as Spaces for Inclusive Communities: A Literature Review. [PDF]
Rodríguez Poveda SP +3 more
europepmc +1 more source
Report of the fact finding Sub-Committee on Libraries [1959]
Report of the Fact Finding Sub-Committee On Libraries -- Introduction -- School Libraries -- Institutional Libraries -- Public Libraries -- Contributing Agencies And ...
Kansas Governor's Steering Committee on White House Conference Planning, Subcommittee on Libraries
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