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New hair regrowth model introduced, imiquimod kills skin cancer cells, T-cadherin loss makes skin cancer more invasive, no strong link between PTCH1 gene and skin cancer after transplant, and male teens more likely to have hereditary hair loss.

New hair regrowth model proposed, imiquimod found to kill skin cancer cells, T-cadherin loss linked to invasive skin cancer, no clear gene link to skin cancer after transplant, and study on children's hair loss shows male dominance and genetic ties.

The document concludes that recognizing and treating cutaneous lupus erythematosus early is crucial for managing the skin and potential systemic symptoms.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

A new diagnostic tool for Vulvovaginal Lichen Planus is highly accurate, and updated treatments for various skin conditions, including melanoma and Hidradenitis Suppurativa, were discussed.

CAP1 decreases the expression of a hair-related protein in young Tan sheep's skin.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

Samcyprone ointment is effective for treating common warts if a sensitization reaction occurs first.

The vitamin D receptor is crucial for bone health and affects various body systems, with mutations potentially leading to disease.

Dehydroepiandrosterone (DHEA) is a prohormone important for producing sex steroids and has potential health benefits.

Modulating BMP activity changes the number, size, shape, and type of ectodermal organs.

Blue light promotes hair growth by interacting with specific receptors in hair follicles.

Loss of a specific protein in skin cells causes symptoms similar to psoriasis.

GRHL3 is important for controlling gene activity in skin cells during different stages of their development.

LEF1 interacts with Vitamin D Receptor, affecting hair follicle regeneration and this could be linked to hair loss conditions.

AIRE-deficient rats developed severe autoimmune disease similar to APECED, useful for testing treatments.

Four patients with a type of rickets and hair loss had different mutations in their vitamin D receptor gene, causing it to not work properly.

The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.

Mice without certain skin enzymes have faster hair growth and bigger eye glands.

A mutation in the Adam10 gene causes freckle-like spots on Hairless mice.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

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

DNA can predict physical traits like eye and hair color accurately, especially in Europeans, but predicting other traits and in diverse populations needs more research.

Sebaceous glands can heal and regenerate after injury using their own stem cells and help from hair follicle cells.

Keratin helps skin cells mature when added to a collagen mix, which could be important for skin and hair health.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

Protein tyrosine kinases are key in male pattern baldness, affecting skin structure, hair growth, and immune responses.

Targeting TGFβ can improve skin immunity in older people.

Mouse profilaggrin helps in skin cell differentiation and may be involved in calcium signaling.

A Korean boy's skin and digestive symptoms were caused by a rare genetic disorder that affects zinc absorption, and he got better with zinc supplements.