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Shorter CAG repeats in a specific gene may increase male hormone activity and symptoms like acne and excess hair in women with PCOS.

Mitochondrial features can predict colorectal cancer outcomes and improve immunotherapy.

Necrobiosis lipoidica may need new criteria for accurate diagnosis due to similarities with another condition.

HSD11b1 affects skin nerves and increases non-histaminergic itch.

The nature of the side chain in RU 58841 derivatives greatly affects its AR affinity, with the N-(iodopropenyl) derivative 13 showing the highest AR binding affinity, suggesting its potential for developing high-affinity radioiodinated AR radioligands.

Testing for CAG repeat polymorphism in the androgen receptor gene is not currently recommended for managing hypogonadism.

HDAC4 and HDAC7 are crucial for Th17 cell development and could be targeted to treat inflammatory diseases.

A 50 mg non-loading dose of ritlecitinib is safe for adults and adolescents.

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

PDO, PLLA, and PCL threads increase collagen in ageing skin but don't change MMP1 gene expression.

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

A man with vitiligo and alopecia saw quick skin and hair improvement with ruxolitinib, but skin color gains were lost after stopping treatment.

The oral contraceptive alone is the preferred treatment for hirsutism, as adding the GnRH analog showed no significant benefit.

Latest articles show advancements in regenerative medicine.

A mouse model for studying scleroderma in chronic graft-versus-host disease was successfully created.

Keratin K6irs is a marker for the inner root sheath of hair follicles in mice and humans.

The 595-nm pulsed dye laser effectively reduces symptoms of EFFC with minimal side effects.

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

Ruxolitinib treatment may cause eyelash growth.

Older age is the main risk factor for hemorrhagic cystitis after stem cell transplants.

CXXC5 is a protein that prevents hair growth and could be a target for hair loss treatment.

Variation in the TCHH gene affects wool curliness in sheep.

UV light makes skin signs of lack of carotene and vitamin A more visible.

Connexin mutations can cause various diseases like hearing loss and skin disorders.

Activating TLR3 may help produce retinoic acid, important for tissue regeneration.