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A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

Substance P may play a role in the inflammation seen in keratosis follicularis spinulosa decalvans.

Mice with a Gsdma3 gene mutation have thicker skin and longer hair follicle openings due to increased β-catenin levels.

A new gene mutation linked to a skin condition was found in a Spanish family.

Hairless protein and putrescine regulate each other, affecting hair growth and skin balance.

A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.

Decreased IGF-1R expression may contribute to sacrococcygeal pilonidal sinus development.

Neuregulin3 affects cell development in the skin and mammary glands.

Lack of Cisd2 disrupts calcium balance in cells, leading to poorly functioning neutrophils.

PrrH sRNA controls pyochelin production in *Pseudomonas aeruginosa*.

Mutations in the ACTB gene cause Becker’s nevi and may lead to muscle issues in Becker’s nevus syndrome.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

Lower SMAD2/3 activation predicts more severe skin cancer.

SOX9 is crucial for cell development and repair but can cause fibrosis and cancer if misregulated.

BMPR1a-ECD reduces wrinkles much more effectively than retinoic acid.

The Notch signaling pathway helps in mouse hair development through a noncanonical mechanism that does not rely on RBPj or transcription.

Finasteride irreversibly affects human steroid 5α-reductase 2, providing insight into its catalytic mechanism and disease-related mutations.

Enzymes that change arginine to citrulline are important for skin barrier and hair formation, and their malfunction can lead to skin conditions and hair disorders.

ULBP3 levels are higher in Tinea capitis patients and may help predict the disease's severity.

Lack of KSR1 stops certain skin tumors in mice.

Saw palmetto may help with prostate issues and hair loss.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

A new mutation in the TRPS1 gene caused Trichorhinophalangeal syndrome in a 17-year-old, highlighting the need for genetic testing.

p63 is essential for activating and differentiating stem cells in the nose's olfactory tissue.

Type II spiral ganglion neurites avoid high concentrations of laminin and fibronectin.

Epimorphin helps shape and develop epithelial cells, like those in hair follicles.

The TT genotype of a specific SNP in sheep is linked to better wool quality.

Matriptase is crucial for skin barrier, hair growth, and may contribute to skin cancer.

miR-133a-3p and miR-145-5p help goat hair follicle stem cells differentiate by controlling NANOG and SOX9.