Results 11 to 20 of about 4,798,414 (293)

Evaluation of Functional T-Cell Assays That Predict Causal Allergens in Eosinophilic Esophagitis

open access: yesDiagnostics
Background: Eosinophilic esophagitis (EoE) is a chronic, food antigen-driven disease of the esophagus that causes considerable morbidity. Elimination of allergenic foods from a patient’s diet is a highly effective treatment.
Julianna Dilollo   +10 more
doaj   +5 more sources

A performance evaluation of commercial fibrinogen reference preparations and assays for Clauss and PT-derived fibrinogen [PDF]

open access: yes, 2002
The wide availability of fibrinogen estimations based on the prothrombin time (PT-Fg) has caused concern about the variability and clinical utility of fibrinogen assays.
Lowe, G.D.O.   +19 more
core   +9 more sources

Functional assays to screen and select monoclonal antibodies that target Yersinia pestis

open access: yesHuman Vaccines & Immunotherapeutics, 2023
Yersinia pestis is a gram-negative bacterium that causes plague in animals and humans. Depending on the route of disease transmission, the bacterium can cause an acute, often fatal disease that has a narrow window for treatment with antibiotics ...
Sergei S. Biryukov   +14 more
doaj   +2 more sources

Predictive chemoproteomics and functional validation reveal Coeae6g-mediated insecticide cross-resistance in the malaria vector Anopheles gambiae [PDF]

open access: yesNature Communications
Sustaining malaria control in Africa is imperilled by the rapid evolution of insecticide resistance in the major vector Anopheles gambiae. Although current genomic and transcriptomic approaches map known resistance alleles, they often lack predictive ...
Sofia Balaska   +8 more
doaj   +2 more sources

Benchmarking deep learning splice prediction tools using functional splice assays [PDF]

open access: yesHuman Mutation, 2020
Hereditary disorders are frequently caused by genetic variants that affect pre-mRNA splicing. Whilst genetic variants in the canonical splice motifs are almost always disrupting splicing, the pathogenicity of variants in the non-canonical splice sites (NCSS) and deep intronic (DI) regions are difficult to predict.
Tabea V. Riepe   +4 more
openaire   +4 more sources

Development of a rapid functional assay that predicts GLUT1 disease severity [PDF]

open access: yesNeurology Genetics, 2018
To examine the genotype to phenotype connection in glucose transporter type 1 (GLUT1) deficiency and whether a simple functional assay can predict disease outcome from genetic sequence alone.GLUT1 deficiency, due to mutations in SLC2A1, causes a wide range of epilepsies. One possible mechanism for this is variable impact of mutations on GLUT1 function.
Zaman, SM   +15 more
openaire   +3 more sources

Compound Functional Prediction Using Multiple Unrelated Morphological Profiling Assays [PDF]

open access: yesSLAS Technology, 2018
Phenotypic cell-based assays have proven to be efficient at discovering first-in-class therapeutic drugs mainly because they allow for scanning a wide spectrum of possible targets at once. However, despite compelling methodological advances, posterior identification of a compound's mechanism of action (MOA) has remained difficult and highly refractory ...
France, Rose   +5 more
openaire   +2 more sources

Andrology: Two functional assays of sperm responsiveness to progesterone and their predictive values in in-vitro fertilization [PDF]

open access: yesHuman Reproduction, 1996
We have recently reported, in a small cohort of subjects, that acrosome reaction (AR) and intracellular free calcium ([Ca2+]i) increase in response to progesterone were significantly correlated with in-vitro fertilization (IVF) rate. In the present study we extended these results to 90 subjects undergoing IVF.
KRAUSZ, CSILLA GABRIELLA   +8 more
openaire   +3 more sources

In vitro functional assays.

open access: yes, 2022
In vitro functional assays.
Miłosz Wieczór (527514)   +26 more
core   +1 more source

Contribution of bioinformatics predictions and functional splicing assays to the interpretation of unclassified variants of the BRCA genes [PDF]

open access: yesEuropean Journal of Human Genetics, 2011
A large fraction of sequence variants of unknown significance (VUS) of the breast and ovarian cancer susceptibility genes BRCA1 and BRCA2 may induce splicing defects. We analyzed 53 VUSs of BRCA1 or BRCA2, detected in consecutive molecular screenings, by using five splicing prediction programs, and we classified them into two groups according to the ...
Théry, Jean Christophe   +14 more
openaire   +4 more sources

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