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BioWorld - Monday, June 1, 2026
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Zebrafish
Neurology/Psychiatric

Novel POMT1 knockout zebrafish model of congenital muscular dystrophy

Oct. 31, 2022
Dystroglycanopathies are a subset of rare congenital muscular dystrophies (CMDs) caused by dysregulation in the assemblage of glycans on the α-dystroglycan (α-DG) transmembrane glycoprotein.
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Brain and DNA
Biomarkers

Researchers find relationship between ITGB8 gene variants and neurogenetic rare disease traits

Oct. 31, 2022
Recent findings have unveiled some integrins are associated with Mendelian conditions. In a recent study, researchers directed efforts toward studying integrin-beta 8 (ITGB8) and its association with pathology, especially with neurological pathology, as none of them have been linked to neuropathology to date.
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cancer cell
Cancer

BBO-8520, a novel KRAS G12C GTP/GDP dual inhibitor

Oct. 31, 2022
Researchers from Bridgebio Pharma Inc. presented preclinical characterization of the novel next-generation KRAS G12C GTP/GDP dual inhibitor candidate, BBO-8520, being developed for the treatment of cancer.
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Lung cancer illustration
Cancer

Preclinical characterization of BAY-2927088 in models of EGFR mutant NSCLC

Oct. 31, 2022
Researchers from Bayer AG presented the discovery of BAY-2927088, a new noncovalent tyrosine kinase inhibitor targeting EGFR exon 20 insertions and C797S resistance mutations in non-small-cell lung cancer (NSCLC).
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Cancer

Bridgene Biosciences reports discovery of BGI-9004, a potent and efficacious covalent pan-TEAD inhibitor for Hippo-altered cancers

Oct. 31, 2022
Targeting TEAD with small-molecule inhibitors is an emerging therapeutic strategy for YAP/TAZ-dependent human cancers with Hippo pathway alterations. Bridgene Biosciences Inc. identified three hits with the Isobaric Mass Tagged Affinity Characterization (IMTAC) screening platform that covalently bound to TEAD1 with the binding site being cysteine 359, which led to the BGI-9004 compound.
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ECTRIMS 2022

Biogen data demonstrates potential of digital health to support MS care

Oct. 28, 2022
By Meg Bryant
Biogen Inc. presented new data showing how applying artificial intelligence (AI), machine learning (ML) and radiomics can produce actionable insights on multiple sclerosis (MS) disease progression. The results, released at this week’s European Committee for Treatment and Research in Multiple Sclerosis (ECTRIMS) Congress, could help to advance new digital health tools to improve monitoring and quality of life of MS patients.
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Brain cross section showing thalamus.
Neurology/Psychiatric

ECTRIMS 2022: Network lens could explain paradox in multiple sclerosis

Oct. 28, 2022
By Anette Breindl
Circuit dysfunction is clearly recognized as a driver of neuropsychiatric disease, and some neurodegenerative diseases such as Parkinson’s disease. And at the European Committee for Treatment and Research in Multiple Sclerosis (ECTRIMS) 2022 Congress, researchers made an argument that the same is true in multiple sclerosis (MS). Such a lens could explain the radiological-clinical paradox between the amount of structural damage and clinical severity.
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Cancer

Preclinical studies support use of TAS-1440 in combination with anti-PD-1 antibodies for treatment of immunotherapy-resistant cancer

Oct. 28, 2022
Lysine-specific demethylase 1A (LSD1) is a monoamine oxidase encoded by the KDM1A...
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DNA illustration
Biomarkers

Pathogenic ELOC gene variants as a novel cause for VHL disease

Oct. 28, 2022
To date, only inactivating germline variations in the VHL gene have been linked to von Hippel-Lindau...
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Cancer

I-0436650, a potent and selective SHP2 allosteric inhibitor for solid tumor treatment

Oct. 28, 2022
Src homology region 2-containing protein tyrosine phosphatase 2 (SHP2) is a target for cancer...
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