Results 191 to 200 of about 63,560 (282)

Meflin/ISLR is a meningeal cell‐specific marker involved in the development of meninges and meningioma progression

open access: yesBrain Pathology, Volume 36, Issue 2, March 2026.
Mesenchymal stromal cell‐and fibroblast‐expressing Linx paralogue (Meflin) is expressed in embryonic meninges and contributes to meningeal homeostasis. In meningiomas, elevated Meflin correlates with higher grade and recurrence. Single‐cell RNA sequencing revealed a Meflin‐high tumor cell subset marked by reduced proliferation, WNT6 expression, and ...
Yukihiro Shiraki   +13 more
wiley   +1 more source

Notch Signalling Plays a Role in Patterning the Ventral Mesoderm During Early Embryogenesis in <i>Drosophila melanogaster</i>. [PDF]

open access: yesInt J Mol Sci
Megaly M   +8 more
europepmc   +1 more source

Precision Oncology for Pediatric Solid Tumors Using In‐Hospital Pediatric/AYA Malignancy‐Specific Panel Sequencing

open access: yesCancer Science, Volume 117, Issue 3, Page 797-806, March 2026.
Our findings indicate that a pediatric/AYA‐specific targeted panel deployed in a hospital can deliver rapid, clinically actionable molecular insights with high diagnostic and prognostic yield. This complements larger sequencing platforms by offering speed, focused content, and easier interpretation.
Masato Kojima   +8 more
wiley   +1 more source

Segregation of endoderm and mesoderm germ layer identities in the diploblast Nematostella vectensis. [PDF]

open access: yesNat Commun
Haillot E   +6 more
europepmc   +1 more source

Kdf1 Regulates Molar Cusp Morphogenesis via the PI3K/AKT/mTOR Signalling Axis

open access: yesCell Proliferation, Volume 59, Issue 3, March 2026.
Epithelial Kdf1 knockout disrupts molar cusp morphogenesis by promoting inner enamel epithelium proliferation and invagination via PI3K/AKT/mTOR signalling. ABSTRACT Keratinocyte differentiation factor 1 (Kdf1) reportedly plays a significant role in enamel formation.
Jiayu Wang   +9 more
wiley   +1 more source

Constructing the spatiotemporal atlas of single-cell lineage trajectories in stereotypic biological structures. [PDF]

open access: yesiScience
Wang R   +10 more
europepmc   +1 more source

A Novel Model System to Identify Cellular and Molecular Defects Underlying Rare Genetic Disorders

open access: yesExperimental Dermatology, Volume 35, Issue 3, March 2026.
ABSTRACT Ankyloblepharon‐ectodermal defects‐cleft lip/palate (AEC) is a disorder caused by autosomal‐dominant mutations in the TP63 gene. AEC is characterised by the presence of severe and painful skin erosions that can take years to heal. Current treatment options for these devastating lesions are limited, highlighting the need for new therapeutic ...
Maddison N. Salois   +4 more
wiley   +1 more source

A chemical epigenetic tool to probe site-specific DNA-binding protein complexes. [PDF]

open access: yesProc Natl Acad Sci U S A
Zhu J   +10 more
europepmc   +1 more source

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