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

Valproic acid and rapamycin protect hair follicle stem cells from damage by activating a protective pathway.

Over-expression of Sp2 can lead to cancer by preventing proper stem cell differentiation.

Sebaceous glands are often preserved and PPARy expression is constant in some cases of Central Centrifugal Cicatricial Alopecia.

Recognizing RSCC is crucial due to its aggressive nature and high risk of poor outcomes.

PF-998425 is a new, effective, and non-phototoxic treatment for skin conditions related to androgens.

Truncated LTBP-1 disrupts TGF-β signaling, affecting hair growth.

FOXC1 boosts SFRP1 in hair loss, suggesting new treatments.

KAP genes show significant genetic variability, but its impact on hair traits is unclear.

Different PIN proteins affect plant root hair growth by changing how auxin is transported.

LTBP1 is a key regulator in diseases and a potential target for new treatments.

Cantú syndrome may be linked to pituitary adenomas.

Deleting part of a gene in mice causes wavy hair and high pup loss.

Pygo2 is important for early growth and progression of intestinal tumors, and could be a target for treating cancers with certain mutations.

Compounds from Pterocarpus indicus may help treat benign prostatic hyperplasia by stopping cell growth.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

KAP genes are crucial for hair development and show both shared and unique traits in humans, chimpanzees, and baboons.

Ca_v1.2 affects hair growth and could be a target for hair loss treatments.

Brg1 is crucial for hair growth and skin repair by maintaining stem cells and promoting regeneration.

KRT14 gene variants cause dermatopathia pigmentosa reticularis, affecting nails, teeth, and hair.

The calcineurin/NFAT pathway plays a significant role in the development and growth of a type of skin cancer called cutaneous squamous cell carcinoma.

Nagashima-type palmoplantar keratosis in Asians is caused by a SERPINB7 gene mutation.

A new therapy for a skin blistering condition has not been developed yet.

Four-amino acid part makes enzyme sensitive to finasteride.

The research showed that CRISPR/Cas9 can fix mutations causing a skin disease in stem cells, which then improved skin grafts in mice, but more work on safety and efficiency is needed.

ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.

The TCL1 transgenic mouse model is useful for understanding human B-cell leukemia and testing new treatments.