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Hair follicle-derived IL-7 and IL-15 are crucial for maintaining skin-resident memory T cells and could be targeted for treating skin diseases and lymphoma.

FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.

Certain immune cells in the skin release a protein that stops hair growth by keeping hair stem cells inactive.

Calcineurin inhibitors, used in kidney transplants, can cause a wide range of side effects including kidney damage and other health issues.

Keratin mutations cause skin diseases and could lead to new treatments.

Heavy ion radiation has a more severe and long-lasting effect on mouse intestinal metabolites than gamma radiation.

Alopecia areata patients have more Propionibacterium acnes and less Staphylococcus epidermidis on their scalps.

A mutation in the IKZF1 gene causes immune system overactivity, linked to autoimmune diseases like lupus.

Early detection of specific skin lesions can help identify Birt-Hogg-Dube syndrome and prevent serious complications.

Genetic variations greatly affect individual metabolism and can impact health and disease risk.

Higher testosterone levels can increase the risk of certain diseases like type 2 diabetes in women and prostate cancer in men, but can also protect against autoimmune diseases and hair loss. It also affects body fat and bone density.

Breathing in high levels of certain air pollutants significantly increases women's risk of developing Polycystic Ovary Syndrome.

Feeling younger can improve health and extend life.

Four new cases of Bachmann-Bupp syndrome suggest potential for targeted treatment.

Researchers found genes and genetic variants linked to sheep wool and skin wrinkles.

Polish medical societies recommend personalized treatment for PCOS based on the patient's specific symptoms and use the Rotterdam criteria for diagnosis.

Certain genes affect udder shape in Holstein cows, important for health and milk production.

Systemic corticosteroids might help treat hair loss caused by alemtuzumab in MS patients.

Oral paclitaxel plus encequidar improved tumor response and caused less neuropathy but more serious infections than intravenous paclitaxel.

MAIT cells may help fight COVID-19 but also contribute to severe inflammation.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

Researchers identified five new potential targets for leishmaniasis treatment, suggesting repurposing existing drugs could be effective.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

Forensic DNA phenotyping can help generate new leads in cold cases but faces accuracy, legal, and acceptance challenges.

Diagnosing and treating PCOS in teenagers is difficult, and the focus is on lifestyle changes and medication to improve health and prevent future issues.

Cutaneous Lymphadenoma is a unique skin tumor with specific protein markers and common gene mutations that may cause continuous cell growth.

People with severe hair loss (Alopecia Areata) have different scalp bacteria than healthy people, which might help predict the condition's progress.

Genetic testing is crucial before giving azathioprine to avoid severe side effects.

Medications for glucose metabolism and weight control, combined therapy options, and herbal medicines may help regulate menstrual cycle in adolescents with PCOS.