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Lymphatic vessels are important for skin repair and could affect skin disease treatments.

Six new genetic regions linked to early hair loss also connect to Parkinson's disease and prostate cancer, possibly leading to new treatments.

The article suggests that targeting specific immune pathways could help control and treat the skin disease hidradenitis suppurativa.

The severity of symptoms in nonclassical congenital adrenal hyperplasia is not determined by CYP21A2 gene variations.

Sardinians were historically short due to a mix of genetics and factors like disease and poor nutrition, but recent height increases suggest better living conditions had a bigger impact.

T cells and bacteria in the gut and skin help maintain health and protect against disease.

YN oil combined with Rhinacanthus nasutus leaf is an effective and safe treatment for dog skin disease.

Lignans and neolignans from plants may help protect against various health issues, including cancer and heart disease.

Prolactin affects hair growth and skin conditions, and could be a target for new skin disease treatments.

The document concludes that understanding sulfation biology is crucial for creating treatments due to its importance in biological functions and disease.

Androgens may influence T cells, contributing to higher autoimmune liver disease risk in women.

The document concludes that anti-dsDNA antibodies are not unique to SLE and their use as indicators is doubtful, highlighting the need for better understanding and classification of the disease.

People with PCOS have higher levels of PAI-1, which may increase their risk of heart disease and fertility issues.

Filaggrin mutations are linked to atopic dermatitis and help explain how genetics and environment affect the disease.

Early treatment of PCOS in teens is crucial to prevent long-term health issues like diabetes and heart disease.

Polycystic Ovary Syndrome (PCOS) can lead to diabetes, heart disease, cancer, and mental health problems.

The nucleus is key in controlling skin growth and repair by coordinating signals, gene regulators, and epigenetic changes.

Organ transplant recipients have a higher risk of skin cancer over time, atopic dermatitis skin shows unusual bacterial and fungal patterns, a new tool for measuring hidradenitis suppurativa severity was created, and gene expression changes in male baldness suggest new treatments.

Early exposure to germs may protect against autoimmune diseases, lack of sex increases alcohol preference in fruit flies, a potential baldness treatment could involve blocking a specific receptor, skin memory cells help prevent re-infection, high-fat diets can affect brain cells related to weight, and the link between social status, stress, and heart disease in primates is unclear.

The vitamin D receptor is involved in multiple body functions beyond calcium regulation, including immune response and rapid reactions not related to gene activity.

The document concludes that the skin's immune system is complex, involving interactions with hair follicles, nerves, and microbes, and can protect or cause disease, offering targets for new treatments.

Women with androgen excess, especially those with PCOS, have a much higher risk of heart disease and stroke.

Hair loss in Androgenetic alopecia (AGA) is due to altered cell sensitivity to hormones, not increased hormone levels. Hair growth periods shorten over time, causing hair to become thinner and shorter. This is linked to miscommunication between cell pathways in hair follicles. There's also a change in gene expression related to blood vessels and cell growth in balding hair follicles. The exact molecular causes of AGA are still unclear.

The document concludes that various treatments for skin conditions are effective, but some require further research, and certain factors like gender and lifestyle can influence disease outcomes.

There is no causal relationship between androgenetic alopecia and serum uric acid.

A mutation in the hairless gene speeds up severe itchy skin in mice on a special diet.

Artemis dysfunction might cause hair loss through telomere shortening.

IL-4 gene variation may increase the risk of alopecia areata in Turkish people.

The first Japanese family with Marie Unna hereditary hypotrichosis showed hair condition improvement in a child and highlighted the risk of misdiagnosis.

The document suggests treating individuals with nonclassic congenital adrenal hyperplasia who show symptoms, especially those related to excess male hormones.