Dermatology Lab · DeCure for X

DeCure for Recessive X-linked ichthyosis

DeCure's autonomous Dermatology AI scientist is researching a drug-repurposing hypothesis for recessive X-linked ichthyosis — screening already-approved drugs against its 2-gene Open Targets disease module to publish open-access research. Research is fast; the path to publication is funded in milestone stages.

Disease module2 genesLead labDermatology
All cures
DermatologyDOID:1700$DeCureDerma

The disease map

Disease moduleRecessive X-linked ichthyosis maps to a 2-gene Open Targets module — the target space DeCure's AI scientist screens approved drugs against.
DeCure.ai methodSignature reversal (LINCS) plus network proximity (STRING) rank already-approved drugs likely to perturb this module — the same engine that produces DeCure.ai's repurposing hypotheses.
Repurposing thesisScreening approved medicines against this disease module, then publishing the evidence for the strongest candidate. Known pharmacology and human exposure data make the first question sharper — they do not establish safety or efficacy in a new indication.

Research record

01
ResearchComing soon
Candidate research + dossier — target rationale, drug-repurposing thesis and evidence pack.proof: Published dossier + on-chain hash
02
ValidationComing soon
In-vitro biological validation at a contract research org (CRO).proof: CRO contract + in-vitro report
03
Peer review & paperComing soon
Peer-reviewed paper published open-access (preprint + journal).proof: DOI + open-access link + on-chain hash

Current lead

No approved-drug candidate for recessive x-linked ichthyosis is corroborated in the literature DeepSearch retrieved. Some conditions are managed with non-pharmacological care — a device, surgery or physical therapy — rather than a medicine; that may be the case here, or the literature we found may simply be too sparse yet to support a drug-repurposing angle.

Molecular view

steroid sulfatase (STS)STS is one of the genes genetically linked to this disease in Open Targets — shown as context, not as a drug target we're pursuing: no approved-drug candidate for this disease is yet corroborated in the literature we found.

Loading structure…
helix sheet bogdrag to rotate · scroll to zoom

RCSB Protein Data Bank · entry 8EG3 · 2.04 Å · ligand octyl beta-D-glucopyranoside (BOG). Experimental structure, not a prediction.

Evidence

Retrieved by DeepSearch across 234,678,978 indexed works and resolved on OpenAlex — ranked by citations, including the results that did not work.

Dermatologica · 2009 · 4 citations

X-Linked Recessive Ichthyosis

AbstractRecent findings in a family with X-linked recessive ichthyosis are presented. The first description of this family in the literature was given and correctly diagnosed by Csörsz in 1928. His paper can be considered one of the most widely cited proofs of the existence of X-linked ichthyosis. The extended pedigree as well as data of steroid sulfatase and arylsulfatase C determinations presented in this paper verify the diagnosis of the X-linked mode of inheritance of ichthyosis in this family. The biochemical investigations carried out on leukocytes of family members resulted not only in a confirmation of the clinico-genetic diagnosis, but they also helped to establish the heterozygous genotype of a female mentioned previously as an affected person.

https://doi.org/10.1159/000248907
Annals of Internal Medicine · 1967 · 0 citations

Genetic Varieties of Ichthyosis.

Abstracts1 May 1967Genetic Varieties of Ichthyosis.R. S. Wells, M.D.R. S. Wells, M.D.Search for more papers by this authorAuthor, Article, and Disclosure Informationhttps://doi.org/10.7326/0003-4819-66-5-1069_3 SectionsAboutPDF ToolsAdd to favoritesDownload CitationsTrack CitationsPermissions ShareFacebookTwitterLinkedInRedditEmail ExcerptDuring the last 4 years a total of 637 patients with various types of ichthyosis have been examined. The majority of these could be classified under one of four headings depending on clinical characteristics and mode of inheritance. Ichthyosis vulgaris (335 patients) is inherited as an autosomal dominant trait and has an estimated frequency of approximately 1 in 1,000 persons. Sex-linked (or more precisely X-linked) ichthyosis (194 patients) was found to have a frequency of approximately 1 in 6,000 men, and it has been established beyond doubt that the gene for sex-linked ichthyosis and that for the Xg blood group... This content is PDF only. To continue reading please click on the PDF icon. Author, Article, and Disclosure InformationAuthors: R. S. Wells, M.D.Affiliations: London, PreviousarticleNextarticle Advertisement FiguresReferencesRelatedDetails Metrics 1 May 1967Volume 66, Issue 5Page: 1069-1069KeywordsAutosomal dominant traitsBlood groupsGenetics ePublished: 1 December 2008 Issue Published: 1 May 1967 PDF downloadLoading ...

https://doi.org/10.7326/0003-4819-66-5-1069_3

Disease module: DeepOracle (Open Targets). Structures: RDKit from PubChem SMILES. Literature: retrieved by DeepSearch across 234,678,978 indexed works (targeted per-candidate search), resolved on OpenAlex.

DeCure is a research and publication project, not medical advice and not a treatment. "DeCure for X" describes a research goal, not a claim that a cure exists. Backing a cure is a contribution to fund the research — it is not an investment, and confers no yield, royalty, equity or IP ownership. Papers are published open-access by the DeCure.ai DAO.