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A trial showed that a new treatment is safe and effective for male pattern baldness, with most participants growing new hair.

THH and PAD type III appear together early in hair growth, but deiminated THH appears later, suggesting another factor is involved.

HPH-15, a new compound, effectively reduces skin fibrosis in experiments without causing harm.

The HSD3B1 variant increases hair loss risk in overweight women with PCOS.

The curly mutation in SELH/Bc mice affects hair and may help study human genetic disorders.

LHTric-1 is a specific antibody useful for studying hair and nail formation.

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.

Understanding and managing side effects of hedgehog pathway inhibitors can improve treatment for advanced basal cell carcinoma.

Genetic mutation and carcinogen treatment are both needed for skin cancer to develop in these specific mice.

Blocking Hedgehog signaling offers new treatment options for advanced basal cell carcinoma.

Targeting NMMHC IIA may help treat blood-brain barrier damage.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

Dihydrotestosterone specifically binds to hamster sebaceous glands, with a higher affinity than testosterone.

Two siblings with a genetic mutation had a form of rickets that doesn't respond to vitamin D.

Vitamin D receptor can control the hairless gene linked to hair loss even without vitamin D.

Bcl-2 affects hair growth and pigmentation by controlling cell death.

FLCN helps control iron levels in cells.

The SHJH hr mice with a mutated Hr gene show signs of faster skin aging due to poor antioxidative protection.

People with Birt-Hogg-Dubé syndrome often have lung problems and delayed diagnosis, and better recognition of CT scan signs could improve diagnosis and management.

Brg1 is crucial for keeping hair follicle stem cells and repairing skin, working with the Sonic Hedgehog pathway to promote hair growth.

Hereditary elliptocytosis causes elongated red blood cells and can lead to mild or no symptoms.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

Hirsutism is excessive male-pattern hair growth in women, often treated cosmetically or with hormone therapy if contraception is also desired.

Two enzymes regulate androgen receptor activity, affecting treatments for androgen insufficiency and benign prostatic hyperplasia.

Researchers found a new mutation causing total hair loss from birth.

TBX3 gene affects horse coat color, with higher expression in darker areas.

New treatments targeting the Hedgehog pathway can help treat advanced skin cancer but may have side effects and their effectiveness in early stages is unknown.

Tmem30b is essential for hearing by maintaining hair cell structure in the ear.

Proper tissue repair in adult skin requires specific histone hypomethylation.