Intestinal mononuclear phagocytes as prognostic biomarker for crohn's disease
US-2024425923-A1 · Dec 26, 2024 · US
US2024018593A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2024018593-A1 |
| Application number | US-202118038915-A |
| Country | US |
| Kind code | A1 |
| Filing date | Nov 29, 2021 |
| Priority date | Nov 30, 2020 |
| Publication date | Jan 18, 2024 |
| Grant date | — |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
Provided are a marker for detecting the severity of atopic dermatitis and a method for detecting the severity of atopic dermatitis using the marker.
Opening claim text (preview).
1 . A method for detecting severity of systemic eruption by atopic dermatitis in a subject, the method comprising: measuring an expression level of a marker for detecting severity of systemic eruption by atopic dermatitis in a subject, wherein the marker for detecting severity of systemic eruption by atopic dermatitis is at least one selected from the group consisting of following genes: TWF1 ADAM15, and SETD1B, and expression products of the genes, wherein the severity is severity of atopic dermatitis corresponding to Excema Area and Severity Index. 2 . The method according to claim 1 , further comprising detecting severity of systemic eruption by atopic dermatitis in the subject based on the expression level of the marker. 3 .- 12 . (canceled) 13 . The method according to claim 1 , wherein the marker is at least one selected from the group consisting of the following genes: TWF1, ADAM15, CIZ1, AND SETD1B and expression products of the genes, and the higher the expression level of the marker is, the worse the severity of systemic eruption by atopic dermatitis in the subject is detected. 14 . (canceled) 15 . The method according to claim 1 , comprising measuring the expression level of the marker in the subject at different time points. 16 . The method according to claim 15 , wherein the marker is at least one selected from the group consisting of the following genes: TWF1, ADAM15, CIZ1, an SETD1B, and expression products of the genes, and when the measured expression level of the marker in the subject is higher than the expression level in the subject at previous measurement, the severity of systemic eruption by atopic dermatitis in the subject is detected to be exacerbated, or when the measured expression level of the marker in the subject is lower than the expression level in the subject at previous measurement, the severity of systemic eruption by atopic dermatitis in the subject is detected to be remitted. 17 .- 33 . (canceled) 34 . The method according to claim 1 , wherein the marker is a nucleic acid marker. 35 . The method according to claim 34 , wherein the nucleic acid is mRNA collected from skin surface lipids.
for diseases caused by alterations of genetic material · CPC title
Expression markers · CPC title
Disease subtyping, staging or classification · CPC title
related to diseases not provided for elsewhere · CPC title
Dermatitis · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.