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Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Betulinic acid can help treat hepatitis C by stopping virus replication.

CEP135 may predict cancer outcomes, and targeting PLK1 could help treat certain sarcomas.

A 37-year-old male with severe skin and internal issues has a rare inherited skin condition called dystrophic epidermolysis bullosa.

Using a combination of specific cell cycle regulators is better for safely keeping hair root cells alive indefinitely compared to cancer-related methods.

Transplanted bone marrow cells actively move, form clusters, and grow after transplantation.

HPV type 56 can hide in hair follicles even without visible warts.

Scientists used stem cells to create a model of the skin disease Epidermolysis Bullosa simplex, which helped them understand its molecular mechanisms and could aid in finding treatments.

Laser treatment for skin conditions VEN and ILVEN is effective and liked by patients.

Chromosomal microarray analysis is important for diagnosing rare genetic variations and guiding treatment.

CRISPR/Cas9 and prime editing can potentially fix skin disorder genes safely and effectively.

HDR electronic brachytherapy effectively treats nonmelanoma skin cancer with good cosmetic results and minimal side effects.

Hair extensions can cause hair loss and scalp damage, and these problems might be more common than people realize.

Pyrene excimer nucleic acid probes are promising for detecting biomolecules accurately with potential for biological research and drug screening.

Most Recessive Dystrophic Epidermolysis Bullosa patients with a specific mutation likely have Sephardic ancestry from about 500 years ago.

TBX3 gene affects horse coat color, with higher expression in darker areas.

DNAJB9 cfRNA could help diagnose and treat female hair loss.

53BP1 focus analysis in hair cells can help estimate radiation doses.

Activin B can boost hair growth by promoting cell proliferation and cell cycle progression.

Targeted therapy with Ustekinumab significantly improved a skin condition called ILVEN, which is caused by mutations in the CARD14 gene.

An extremely low-birthweight infant had a rare genetic skin disease and died despite treatment.

Giving immune serum from vaccinated mice to mice without T cells prevents infection and tumor growth.

Mutations in the KLHL24 gene cause skin blistering in epidermolysis bullosa simplex.

Epigenetic changes in blood cells may contribute to alopecia areata.

Hair follicle cells produce VEGF, which can promote blood vessel cell growth and movement.

The vector successfully directed specific gene expression in hair follicles.

A common mutation in the hHb6 gene is linked to monilethrix, but other factors may also play a role.

Small amounts of DNA can be found in the hair shaft, especially near the root, but it decreases with hair treatments and washing.

A specific gene mutation causes a severe skin disorder in a family.