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Resultados 75 resultados
LastUpdate Última actualización 15/06/2025 [06:47:00]
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Solicitudes publicadas en los últimos 30 días / Applications published in the last 30 days
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DETECTION OF DISEASE STATE MACROMOLECULES BINDING TO NORMAL MACROMOLECULES AS A BIOMARKER FOR DISEASE IDENTIFICATION

NºPublicación:  WO2025080894A1 17/04/2025
Solicitante: 
VERAVAS INC [US]
PHANES BIOTECH INC [US]
VERAVAS, INC,
PHANES BIOTECH, INC
WO_2025080894_PA

Resumen de: WO2025080894A1

In one aspect, the present disclosure provides a method of detecting a presence or absence of a biomarker for a disease in the sample, wherein the biomarker comprises: a) a complex of physiologically active target macromolecules or a fragment or portion thereof and target macromolecules that are not physiologically active; b) a conformation of the physiologically active macromolecules or fragment thereof when the physiologically active target macromolecules or the fragment or portion thereof is a complex with a non- physiologically active target macromolecule; c) the conformation of physiologically active target macromolecules or a portion or fragment thereof in a PAT-Tau complex; d) the conformation of non-physiologically active target macromolecules or a portion or fragment thereof in a PAT-Tau complex; or e) a combination of a), b), c), d) and/or e).

EPIGENOME BIOMARKERS FOR IDENTIFYING ALZHEIMER'S DISEASE

NºPublicación:  US2025122570A1 17/04/2025
Solicitante: 
SALK INST FOR BIOLOGICAL STUDIES [US]
Salk Institute for Biological Studies
US_2025122570_PA

Resumen de: US2025122570A1

Methods are provided for identifying Alzheimer's disease cells or subjects, based on the methylation status of multiple methylation markers in genomic DNA. Also provided are methods for identifying therapeutic agents for treating Alzheimer's disease by monitoring changes in the methylation status of multiple methylation markers.

Supermere Nanoparticles and Methods of Isolation and Use Thereof

NºPublicación:  US2025123297A1 17/04/2025
Solicitante: 
VANDERBILT UNIV [US]
Vanderbilt University
US_2025123297_PA

Resumen de: US2025123297A1

Disclosed herein is a newly identified secreted nanoparticle that is morphologically and molecularly distinct from the recently described nanoparticle termed an exomere. The disclosed nanoparticle is referred to herein as a supermere. Both exomeres and supermeres are amembranous in contrast to membrane-enclosed extracellular vesicles (EVs). Supermeres are smaller and morphologically distinct from exomeres. These supermeres contain cargo with diagnostic and therapeutic applications.

A Beta Biomarker of Alzheimer’s Disease Model Mouse and Analysis Method Thereof

NºPublicación:  US2025123296A1 17/04/2025
Solicitante: 
SHIMADZU CORP [JP]
THE UNIV OF TOKYO [JP]
Shimadzu Corporation,
The University of Tokyo
US_2025123296_A1

Resumen de: US2025123296A1

A level of mouse Aβ1-40 and a level of mouse APP669-711 in a biological sample derived from an AD model mouse are measured by detection of markers including mouse Aβ1-40 and mouse APP669-711; an APP669-711/Aβ1-40 ratio which is a ratio of the level of mouse APP669-711 to the level of mouse Aβ1-40 is calculated; and when the ratio in the AD model mouse is higher than the same ratio in a reference mouse in which cerebral Aβ deposition is absent, it is judged that an amount of cerebral Aβ deposition in the AD model mouse is higher than an amount of cerebral Aβ deposition in the reference mouse.

METHODS FOR DETECTING B-ISOX PRECIPITATES OR CAPTURED PROTEINS AS BIOFLUID BIOMARKERS

Nº publicación: EP4537112A1 16/04/2025

Solicitante:

YEEFAN MED INC [US]
YeeFan Med Inc

AU_2023294616_PA

Resumen de: AU2023294616A1

Described herein are detecting methods for conformational disease, aging and proteinopathies, by measuring the presence of b-isox-precipitates and the levels of b-isox-captured proteins in biofluids of healthy individuals and patients. Research identified additional biomarkers, which made it possible to detect, diagnose or treat, a human disease in a human subject by, with or without adding an isoxazole to an obtained biofluid sample, detecting the biomarker. Use of b-iso and/or biomarkers for diagnosing the disease are made possible.

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