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A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

A new mutation linked to partial Androgen Insensitivity Syndrome and prostate cancer was found in a patient unhappy with their female gender assignment.

New LSS gene variants help understand congenital hypotrichosis 14 better.

Noncoding dsRNA boosts hair growth by activating TLR3 and increasing retinoic acid.

The Wave complex controls skin growth by suppressing certain signals.

Rose stem cell nanoparticles improve skin quality by boosting collagen, aiding cell movement, reducing melanin, and lowering inflammation.

Delta-opioid receptors affect skin cell circadian rhythms, possibly impacting wound healing and cancer.

Ptprq has multiple forms that change during inner ear development.

Certain mutations in the hairless protein disrupt its ability to regulate the hair cycle.

QSOX enzymes help form protein bonds in cells, especially in tissues with high secretory activity.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

Researchers found a genetic region that influences the number of coat layers in dogs.

Alopecia areata patients have lower SOX9 and CD34 levels, affecting hair growth.

Steroid sulfatase is important for activating hormones that affect memory, brain function, and certain diseases, and could be a target for treating hormone-related disorders.

The hair keratin gene KRT81 is found in both normal and breast cancer cells and helps them invade surrounding tissues.

Sox10 is important for hair follicle development and hair growth cycles.

The SOSTDC1 gene is crucial for determining sheep wool type.

Selenium in proteins helps prevent over-oxidation and supports chemical reversibility.

CXXC5 can both suppress and promote cancer, making it a complex target for treatment.

Faulty Notch signalling may cause hair follicle changes and inflammation in hidradenitis suppurativa.

A specific RNA molecule, circCOL1A1, affects the growth and quality of goat hair by interacting with miR-149-5p and influencing cell growth pathways.

SARMs may be an effective treatment for a certain type of breast cancer by blocking cancer growth and spread.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

A patient with Rhupus was diagnosed with Rowell syndrome and treated with various medications.

Testosterone reduces knee movement, while flutamide and finasteride increase it.

The study found key genes and pathways involved in cashmere goat hair growth stages.

The hairless (hr) gene is essential for normal hair follicle function and its mutation leads to hair loss.