Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Somatic mutation in RUNX1 underlies mucocutaneus inflammatory manifestations.

Rheumatology (Oxford, England) - 1 Dec 2021

Okano Tsubasa, Nishimura Akira, Inoue Kento, Naruto Takuya, Tokoro Shown, Tomoda Takahiro, Kamiya Takahiro, Simbo Asami, Akutsu Yuko, Okamoto Keisuke, Yeh Tzuwen, Isoda Takeshi, Yanagimachi Masakatsu, Kajiwara Michiko, Imai Kohsuke, Kanegane Hirokazu, Mori Masaaki, Morio Tomohiro, Takagi Masatoshi

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Child
Share to Child, Preschool
Share to Core Binding Factor Alpha 2 Subunit

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Dermatitis

Share to Mutation

Share to Myelodysplastic Syndromes

Share to Whole Genome Sequencing

Source

Identifiers

PMID: 34528076
DOI: 10.1093/rheumatology/keab513

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Somatic mutation in RUNX1 underlies mucocutaneus inflammatory manifestations.PMID 34528076Read ↗

Myeloid and lymphoid neoplasms with FGFR1 abnormalities: diagnostic and therapeutic challenges.Semantic proximity Read ↗

Disease mutations in RUNX1 and RUNX2 create nonfunctional, dominant‐negative, or hypomorphic allelesSemantic proximity Read ↗

Variable phenotypic manifestation of IRF6 mutations in the Van der Woude syndrome and popliteal pterygium syndrome: implications for genetic counseling.Semantic proximity Read ↗

Natural history of GATA2 deficiency in a survey of 79 French and Belgian patientsSemantic proximity Read ↗

De Novo 21q22.1q22.2 deletion including RUNX1 mimicking a congenital infection.Semantic proximity Read ↗

A novel homozygous RAG1 mutation in a girl presenting with granulomas and alopecia capitis totalis.Semantic proximity Read ↗

New insights into the role of Runx1 in epithelial stem cell biology and pathologySemantic proximity Read ↗

Making sense of giant cell lesions of the jaws (GCLJ): lessons learned from next-generation sequencing.Semantic proximity Read ↗

MUC1-C Oncoprotein Integrates a Program of EMT, Epigenetic Reprogramming and Immune Evasion in Human CarcinomasSemantic proximity Read ↗

TRNT1 missense mutations define an autoinflammatory disease characterized by recurrent fever, severe anemia, and b-cell immunodeficiencySemantic proximity Read ↗

Oral and maxillofacial manifestations of lipoid proteinosis with a novel ECM1 mutation: case report and literature review.Semantic proximity Read ↗

Invasive mucorales sinusitis in a young patient with Emberger syndrome and newly diagnosed AML: A case report and literature review of invasive fungal infections in GATA2 deficiency.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.