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Overexpression of SSAT causes hair loss and skin issues, but reducing putrescine can help.

αCT1 improves scar appearance by changing early collagen structure.

Involucrin helps strengthen the inner parts of human hair.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

A new hydrogel with stem cells can repair damaged uterine lining and improve fertility.

Centipeda minima and brevilin A protect skin cells from damage and aging.

The study concluded that the arachidonic acid pathway and the protein KRT79 play a role in determining the fineness of cashmere.

POMC-derived peptides are important for skin functions like immune response and stress management.

Sesn2 protects inner ear hair cells from damage by regulating certain cell survival pathways.

LPA3 signaling in the uterus is crucial for placental formation and fetal development.

Transglutaminase does not modify human hair.

Human hair keratin has a 40% α-helix structure that changes to a random coil in 8 M urea.

BMP signaling is essential for the development of touch domes.

PKM2 is a promising target for heart repair and regeneration.

Extracellular vesicles from mammary cells help heal skin wounds effectively.

Most patients experienced mild to moderate skin problems during a trial for a desmoid tumor treatment.

Laminin, type IV collagen, and fibronectin help develop skin and hair structures in embryos.

Combining DHT and EDC improves the strength and stability of PADM scaffolds for tissue engineering.

A gene mutation in mice causes hair loss, weak bones, and protein buildup, showing how protein processing issues can lead to diseases.

A fatty acid/protein complex in human hair helps protect it from damage.

Lymphotoxin-β is crucial for proper skin development in embryos.

Laminin 332 is essential for normal skin cell behavior and structure.

Involucrin gene expression is controlled by specific proteins and signaling pathways.

MSC-protein helps regenerate gum tissue and bone.

A new method, iSiMPRe, effectively identifies key protein regions in cancer genes, highlighting potential drug targets.

Apoptosis is essential for human skin development and forming a functional epidermis.

Mutations at Val-889 and Arg-752 disrupt key interactions in the androgen receptor, affecting its function.

Mouse and human skin development share similar fibroblast timelines.

L-PGDS has specific binding sites for its functions and could help in drug delivery system design.