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Researchers discovered how to control Claudin expression in cells, aiding cancer and regenerative medicine research.

A hairless patch on a boy's scalp from birth injury improved with minoxidil treatment.

Reduced AhR signaling in HS tunnels leads to persistent inflammation and microbial imbalance.

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

Airway issues can occur in Conradi–Hünermann–Happle syndrome and can be managed with minimally invasive procedures.

Specific mutations in a receptor cause facial abnormalities and hair loss.

Mutations in Plcd1 and Plcd3 together cause severe hair loss in mice.

A severe medication reaction required long treatment and led to hair loss and thyroid issues.

Scalp rolling might help regrow hair in people with a hair loss condition called Alopecia Areata.

Scientists found a gene in mice that causes early hearing loss.

A new genetic disorder caused by an ODC1 mutation can be treated with DFMO.

The model improves understanding of androgen interactions by focusing on signal intensity and system capacity.

Trichothiodystrophy is a rare genetic disorder causing hair issues and sometimes linked to DNA repair defects.

Thyroid hormone (T3) may reverse gray hair by stimulating hair growth.

Trichothiodystrophy hair is structurally abnormal with protein and organization issues.

A five-month-old boy with Omenn syndrome successfully recovered after a stem cell transplant with reduced intensity conditioning.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.

Intravenous calcium therapy is a safe and effective treatment for a rare type of rickets.

Ritlecitinib helps regrow hair in alopecia areata and is safe for long-term use.

The hr gene is linked to hair loss in Valle del Belice sheep.

Blocking 5α-reductase can reduce sleep deprivation-related behavioral issues in rats.

The ABHRS has outlined its goals for the next year.

Genetic marker rs12558842 strongly linked to male hair loss.

Robertsonian translocation can cause recurrent miscarriages.

Diagnosing and managing Glucocorticoid Resistance Syndrome is complex due to genetic differences and varied symptoms.

Hair loss can be a key sign of a rare type of rickets when vitamin D treatment doesn't work and advanced tests aren't available.

Persistent hyperparathyroidism doesn't stop rickets healing or phosphate level normalization in VDDR2A.

The TRPV3 gene mutation affects hair growth by keeping mice in the growth phase longer, which could help treat hair loss.

ODC transgenic mice can model human hair loss with skin lesions.