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Gender-diverse people face more depression and anxiety, partly due to stress and lower cortisol levels.

Overactivating Hedgehog signaling makes hair follicle cells in mice grow hair faster and create more follicles.

The vitamin D receptor can affect gene activity even without its usual hormone in hair and skin.

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

The conclusion is that metformin is a first-line treatment for PCOS, particularly for restoring ovulation and increasing pregnancy rates, with other treatments depending on specific symptoms.

GLI1 might protect against the start of skin cancer and is not linked to cancer severity.

Hair loss in Telogen effluvium is often chronic, linked to stress, and lacks a confirmed treatment, but topical corticosteroids may be used.

A gene mutation causes monilethrix in a Chinese family.

Sox9 levels in brain stem cells affect whether they stay as stem cells or become neurons.

Diagnosing both systemic lupus and hemoglobinopathy is challenging due to overlapping symptoms.

Personalized sonidegib dosing can effectively treat Gorlin-Goltz syndrome with fewer side effects.

Mutations in the LIPH gene cause woolly hair in a child.

PCOS is a common hormonal disorder causing irregular periods and increased hair growth, linked to insulin resistance and long-term health issues.

Researchers found four distinct fibroblast types in human skin, which could help in treating wounds and fibrotic diseases.

Understanding different types of skin cells, especially fibroblasts, can lead to better treatments for wound healing and less scarring.

Keloid scars are aggressive, excessive skin scars with unique features and complex diagnosis.

Skin cells called dermal fibroblasts are important for skin growth, hair growth, and wound healing.

Ultrasonography improves pilomatricoma diagnosis accuracy.

New single-cell analysis techniques are improving our understanding of stem cells and could help in treating diseases.

Mutations in the DSG4 gene cause specific hair and scalp issues.

Stem cells are crucial for tissue growth, cancer treatment, and disease modeling, but challenges remain in clinical use.

Mercuric triflate is an effective catalyst for various organic reactions, working well at room temperature with high yields.

mHa2 and mHa3 keratins have different structures and roles in mouse hair and tongue tissues.

Targeted protein degraders show promise in treating cancer but need to target more diverse proteins.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

Melanoma's complexity requires personalized treatments due to key genetic mutations and tumor-initiating cells.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

Fibrodysplasia ossificans progressiva is a rare genetic disorder that causes extra bone growth and symptoms of premature aging.

Studying premature aging syndromes helps understand human aging and suggests potential treatments.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.