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Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

New cancer treatments show promise in reducing tumor growth and improving skin regeneration in mice.

Triangular temporal alopecia can occur in adults and should be correctly identified to prevent misdiagnosis.

Deep phenotyping helps distinguish between xeroderma pigmentosum and trichothiodystrophy, aiding in diagnosis and treatment.

A new compound shows promise as a topical treatment for hair loss.

The research found a way to identify and study skin cells with stem cell traits, revealing they behave differently in culture and questioning current stemness assessment methods.

The arrector pili muscle attaches to the extracellular matrix using α5β1 integrin and connects muscle cells using α1β1 integrin.

Keratin's mechanical properties are influenced by hydrogen bonds and secondary structure, and can be improved with the SPD-2 peptide.

Phospholipase Cδ1 is crucial for normal skin and hair development.

TRPV3 and TRPV6 channels change structure to regulate calcium and heat responses.

A more sensitive assay was developed to detect enzyme activity converting arginine to citrulline in hair follicles.

A new peptide, murikal/SPR4, was found to significantly increase hair growth in mice, and its liposomal topical formulations enhanced hair growth more than commercial products. However, results on human scalp skin were unclear, needing more tests.

KAP8.1 protein is crucial for hair structure and interacts with keratin 85.

Resident memory T cells and necroptosis may drive fibrosis in eosinophilic fasciitis and morphea.

GLP-1RAs, like semaglutide and tirzepatide, may cause hair loss, so patients should be informed and monitored.

A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

Angiopoietin-1 helps hair cells survive and grow, making it a potential treatment for hair loss.

Lack of cystatin M/E causes thin hair and dry skin.

NAC1 controls certain enzymes that reduce root hair growth in Arabidopsis.

Peficitinib can turn human fibroblasts into cells that help grow hair.

Carriers of a specific gene mutation have subtle skin changes without visible symptoms.

The PTGER2 gene is highly active in Cashmere goat skin and its activity changes with the hair growth cycle.

Monilethrix is a genetic disorder causing brittle hair, diagnosed using tricoscopy.

Higher levels of nidogen1 and type IV collagen are found in basal cell carcinoma compared to normal skin.

IP-PA1 helps grow hair in mice and affects human cell growth-related genes differently than traditional hair growth treatments.

PrPC is important for neural differentiation in cattle and mouse embryonic stem cells.

Monilethrix is linked to a gene cluster on chromosome 12.

Intralesional triamcinolone acetonide is more effective than platelet-rich plasma for treating scalp alopecia areata.