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The N363S gene variant does not cause higher adrenal androgen levels in women with polycystic ovary syndrome.

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

Maize hybrids show better early growth due to complex gene interactions from their parent strains.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

No clear link between specific gene and hair loss in Mexican brothers.

Molecular diagnostics help identify genetic defects causing endocrine diseases, improving diagnosis and treatment options.

Advanced imaging techniques are crucial for accurately diagnosing Monilethrix, a rare hair disorder.

Furless male rabbits grew slightly faster and heavier than furred ones, but testosterone levels were not the cause.

A baby girl has a hair disorder called monilethrix, causing fragile hair that may improve over time.

A 12-year-old girl in Saudi Arabia with Focal dermal hypoplasia showed skin and dental symptoms, highlighting the condition's variability and the need for personalized treatment.

Genetic testing confirmed a young girl has Atrichia with Papular Lesions due to mutations in the hairless gene.

Rothmund-Thomson syndrome type 2 can cause chronic, poorly healing wounds.

UV radiation may cause DNA changes in skin, certain UVB therapy helps psoriasis, a new gene mutation is linked to mild piebaldism, different immune cells affect psoriasis, a drug promotes hair growth, and some cancer drugs could treat skin barrier issues.

The document concludes that an experimental drug may help wound healing in Epidermolysis Bullosa, links Hydroa vacciniforme to EBV, discusses diagnosing hair loss disorders, finds many children with eczema have allergies, reviews the safety of a skin medication in children, notes side effects of a Duchenne's treatment, and identifies a marker for pediatric mastocytosis.

Benzoyl peroxide and adapalene gels work differently to reduce acne in mice.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

PTHrP is important for bone formation and may be targeted for osteoporosis treatment and longevity therapies.

Mice without the vitamin D receptor have bone issues and other health problems, suggesting vitamin D is important for preventing various diseases in humans.

Removing the ATR gene in adult mice causes rapid aging and stem cell loss.

Nerve signals are crucial for hair follicle stem cells to become skin stem cells and help in wound healing.

The research found that different types of fibroblasts are involved in wound healing and that some blood cells can turn into fat cells during this process.

The circadian clock affects skin stem cell behavior, impacting aging and cancer risk.

Certain proteins, Lgr5 and Lgr6, are important markers of adult stem cells and are involved in tissue repair and cancer development.

TRPA1 is crucial for mechanical sensitivity in skin sensory neurons.

Removing part of the vitamin D receptor stops vitamin D from working properly.

The research shows that a gene called Wnt3 affects hair growth and structure, causing short hair and balding when overactive.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Wnt1/βcatenin signaling is crucial for heart repair after injury.

A protein from certain immune cells is key for new hair growth after skin injury in mice.

Understanding where cancer cells come from helps create better prevention and treatment methods.