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Lamins are vital for cell survival, organ development, and preventing premature aging.

Regenerative pharmacology, which combines drugs with regenerative medicine, shows promise for repairing damaged body parts and needs more interdisciplinary research.

Damaging mitochondrial DNA in mice speeds up aging due to increased reactive oxygen species, not through the p53/p21 pathway.

Three new types of a skin blistering disease were found, caused by specific gene mutations.

Fine wool sheep have more genes for wool quality, while coarse wool sheep have more for skin and muscle traits.

Many survivors of Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis in Togo suffer long-term eye and skin problems.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

Acne is a common skin condition linked to diet, hormones, and genetics, and early treatment can prevent scarring.

The document concludes that better tools are needed to measure skin disease severity in dermatomyositis and cutaneous lupus erythematosus, and introduces the DSSI and CLASI as reliable instruments.

NF-κB signaling is crucial in many diseases and can be targeted for new treatments.

Sodium hypochlorite can effectively prevent and remove Staphylococcus aureus biofilms in atopic dermatitis at high enough concentrations.

Anorexia Nervosa and Bulimia Nervosa are complex eating disorders with increasing incidence among young females, significant morbidity, and varying mortality rates, requiring more research for better treatment.

Progeroid mouse models show signs of early aging similar to humans, helping us understand aging better.

Epidermal stem cells help heal severe skin wounds and have potential for medical treatments.

Sarcoidosis is more common and severe in Black patients than in Caucasians, requiring early diagnosis and treatment.

Fibroblasts are crucial for tissue repair and inflammation, and understanding them can help treat fibrotic diseases.

Damaging mutations in NFKB2 cause a severe and distinct form of primary immunodeficiency with early-onset and often ACTH-deficiency.

Type 1 diabetes often occurs with other autoimmune diseases, and personalized treatment based on genetics can improve outcomes.

The oncoprotein causes abnormal hair growth without increasing skin cancer risk.

New targeted immunotherapies are improving treatment for inflammatory skin diseases.

COVID-19 can cause different types of hair loss, and proper diagnosis by a specialist may be needed.

Most patients with autoimmune blistering diseases experienced some hair loss, which may be underreported and linked to disease severity.

Trichoscopy is a tool for detailed examination of hair and scalp diseases.

COVID-19 can cause different types of hair loss, which may last up to 100 days, and treatments are still being explored.

Dilated follicular infundibula and increased catagen/telogen follicles are key indicators for diagnosing alopecia areata.

A girl with red hair developed hair-pulling and body image disorders after being bullied for her hair color.

Hair loss in autoimmune blistering skin diseases varies and may regrow with disease control.

Some new oral anticoagulants may also cause hair loss and might not be better than traditional ones for preventing hair loss.

ILK is essential for proper hair follicle development and structure.

Focal atrichia helps diagnose female pattern hair loss.