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SHPro® improved urinary symptoms and erectile function in men and is safe.

Hair loss may indicate higher risk of heart disease.

Five new mutations in the androgen receptor gene were found, helping to understand androgen insensitivity syndrome better.

Mutations in the androgen receptor gene cause Androgen Insensitivity Syndrome, affecting sexual development.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

Alopecia areata patients show unique protein activity patterns, suggesting imbalanced signaling pathways.

CARI ONE helps start hair growth and makes hair follicles bigger and more numerous.

Reduced SIRT1 in hair cells may cause alopecia areata by triggering immune responses.

The ASIP gene is crucial for determining cattle coat color.

All parts of the CLASI-A score are important for assessing skin activity in cutaneous lupus erythematosus.

Certain interactions help prepare the androgen receptor for pairing and activation, which is important for its role in development and disease.

Syndecan-1 is essential for maintaining skin fat and preventing cold stress.

Hair evaluation is crucial for early diagnosis and management of ARCI, as hair loss often indicates severity.

High amphiregulin in the skin is a bad sign for acute graft-versus-host disease.

AC5 improves hair loss and hair quality with high satisfaction rates.

The SYP123-VAMP727 complex is important for transporting materials that harden the root hair shank in Arabidopsis.

A man with hypoparathyroidism had other health issues that led to a diagnosis of a rare autoimmune disorder, APS-1.

Hairless protein helps control hair growth by regulating vitamin D receptor activity.

The SNP rs6457452 is linked to a higher risk of alopecia areata in Koreans.

A JAK1 variant causes hair loss, skin issues, and thyroid disease, but treatment with a specific inhibitor can help.

We need better ways to test and understand SARMs to make safer and more effective treatments.

A 27-year-old with APS-1 showed improvement in symptoms after treatment.

A mutation in the SREBF1 gene causes both hereditary mucoepithelial dysplasia and IFAP syndrome, which are related conditions.

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

Acetylcholine receptors might be involved in the development of acne inversa and smoking could worsen the condition.

Blocking certain receptors in the lungs might help treat a specific type of asthma.

ADF8 and ADF11 help root hairs grow by responding to hormones and environmental signals.

1% anthralin ointment is effective and safe for treating severe alopecia areata in children.