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Exosomal miR-199a-3p from dermal papilla cells helps control hair color by affecting melanocytes.

DAB labeling effectively identifies collagen type III and PDGFR in horse skin, but may show false positives.

Exosomal miR-222-3p reduces melanin production in rabbits by targeting the SOX10 gene.

New compounds were made that block an enzyme linked to breast cancer better than existing treatments.

TTD patients don't have a higher skin cancer risk because their main issue is with transcription, not DNA repair.

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

The report expanded knowledge of MBTPS1-related disorders by identifying new symptoms.

Rhizobacterial strain RT3 helps lettuce survive drought by producing protective substances like proline.

Basonuclin is crucial for hair follicle development and cycling in mice.

OsUEV1B protein is essential for controlling phosphate levels in rice.

Long-read RNA sequencing can identify complex gene changes in IFAP syndrome.

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

CENPV, a new partner of CYLD, helps regulate ciliary acetylated tubulin and is overexpressed in certain skin tumors.

UBC13 and UBC22 enzymes are important for plant growth and development in Arabidopsis thaliana.

CI-1033 causes skin lesions in rats, similar to humans, due to EGF receptor inhibition.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

μ-Crystallin may help hair growth by affecting thyroid hormone levels in mouse hair follicles.

Dicer is crucial for hair growth in mice.

A specific gene mutation causes a severe skin disorder in a family.

Overexpression of LRIG3 in skin causes hair loss.

Trichothiodystrophy involves brittle hair due to low sulfur amino acids, not a transport defect.

Thyroid hormone receptor β1 is found in human hair follicles and helps them survive.