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ALRN-6924 may prevent hair loss caused by chemotherapy.

A KLK5 inhibitor effectively improved skin symptoms in a mouse model of Netherton Syndrome.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

Mice with human-like EGFR had growth issues, skin defects, heart problems, and unusual bone development.

p120-catenin helps control skin inflammation by regulating cadherin levels.

Skin organoids with NCSTN mutation show changes in hair follicle development and higher inflammation, key features of Hidradenitis Suppurativa.

A new method for studying hair follicles is easier and more precise, useful for hair loss and cancer treatment research.

Researchers created specific antibodies that detect a protein important in development and various conditions, and can be used for research and diagnosis.

Keratin 79 is linked to liver damage and may help diagnose liver diseases.

Human hair proteins have similar cysteine and glycine levels to skin proteins.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

LGR6+ stem cells may improve bone healing.

Lithium chloride-treated stem cell exosomes boost hair growth by activating a specific pathway.

Protein-losing enteropathy worsened with lupus symptoms but improved with prednisolone.

rwSALT accurately measures hair regrowth in alopecia areata using scalp photos.

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

The STIM1 R304W mutation in mice leads to bone changes and teeth hair growth.

The commentary explains that a balance of HR protein and putrescine is important for normal hair growth.

Disrupting the Sox21 gene in mice causes hair loss and regrowth cycles.

Exosome-based therapies could help treat hair loss, but more research is needed.

The protein ARA70/ELE1 is involved in male pattern baldness, and lower levels of its short form may lead to hair thinning.

Certain genetic variants reduce enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

Non-coding RNAs help control hair growth in cashmere goats.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

hsa-miR-193a-5p may help diagnose and treat alopecia areata.

ME1 and PPAR signaling may influence hair loss in androgenetic alopecia.

Platelet lysate is better than fetal bovine serum for growing stem cells and healing wounds.

The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.