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The consensus provided guidelines for treating the Female Athlete Triad and a system to decide when athletes can return to sports.

New genetic locations explain much of hair color variation in Europeans.

Ancient DNA blocks are still present in human genomes, possibly due to advantages they provide.

Enhancers and super-enhancers are key in controlling specific gene activity and can play a role in cancer development.

Aging slows wound healing due to weaker cells and immune response.

Non-coding RNAs are crucial for skin development and health.

Vitamin D receptor is important for regulating hair growth and wound healing in mice.

Human hair follicles can be used to create stem cells that might help clone hair for treating hair loss or helping burn patients.

Thymic mesenchymal cells have unique gene expression that supports their specific functions in the thymus.

A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

All five human steroid 5α-reductase enzymes are found in the endoplasmic reticulum.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

The gene NM_026333 slows down aging by affecting the NCX1 pathway and could be targeted for anti-aging treatments.

Blocking certain immune signals can reduce skin damage from radiation therapy.

PPARγ is essential for maintaining healthy skin, controlling inflammation, and ensuring proper skin barrier function.

Reductive stress messes up collagen balance and alters cell signaling in human skin cells, which could help treat certain skin diseases.

KAP genes are crucial for hair development and show both shared and unique traits in humans, chimpanzees, and baboons.

Eyelid cells share signaling components but differ in pathway activity.

Shorter telomeres in white blood cells may increase the risk of a common type of hair loss.

Magnesium supplements improved quality of life for women with polycystic ovary syndrome, but didn't help with acne, hair loss, or abnormal bleeding.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

Different types of PCOS need specific diagnosis methods and treatments.

A gene mutation in Lama3 is linked to a common type of hair loss.

A man with kidney tumors and lung cysts was diagnosed with Birt–Hogg–Dubé syndrome and treated successfully, with genetic testing confirming the diagnosis.

Scientists made nanoparticles from human hair proteins to improve drug delivery.

Common variants in the Trichohyalin gene are linked to straight hair in Europeans.

Different small areas within hair follicles send specific signals that control what type of cells stem cells become.

A new keratin, hK6irs1, is found in all layers of the hair follicle's inner root sheath.

The review suggests that while many AKR1C3 inhibitors show promise for treating certain cancers, more research is needed to confirm their effectiveness in humans.

New treatments are needed for PCOS that target its genetic, hormonal, and metabolic causes.