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The BMP2 gene is more active in the early growth phase of Cashmere goat hair and may affect hair regeneration and textile production.

EF and PXE not closely related.

A specific mutation in PA-PLA1α causes abnormal hair growth.

EMS and EF both show similar skin and fascia changes, but EMS has more severe symptoms and nerve inflammation.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

Keratin-associated proteins are part of the developing hair fiber cuticle.

Changes in the HR gene have influenced hair growth and may lead to hair loss conditions in humans.

The document says menstruation is important for women's health, discusses menstrual disorders, and suggests personalized treatment options.

Women with congenital adrenal hyperplasia showed no prostatic growth.

Dirty dots are a common scalp finding in elderly women and can be washed away with shampoo.

TGF-alpha is present in sheep and ferret skin and may affect hair growth without directly stimulating cell proliferation.

The study suggests that complement activation, not immunoglobulins, may be important in erythema nodosum leprosum.

Becker's Nevus Syndrome is a rare condition with a skin patch and possible bone and muscle abnormalities, treated mainly for appearance.

A 12-year-old boy with a rare genetic condition has progressive hair loss with no effective treatment.

Krt16-deficient mice help understand skin disorders like PC and FNEPPK.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

Hair restoration, especially at the hairline and frontal hair volume, can improve facial balance and attractiveness, with follicular unit transplantation being a successful method.

Different versions of the KRTAP6-2 gene in goats can lead to thinner cashmere fibers.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

A 17-year-old girl and her brothers have a rare hair condition with long eyelashes, thick eyebrows, and easily pluckable hair.

Human skin has less GDNF and its receptor with age.

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

Collagen is crucial for health and treating certain diseases, and supplements can improve skin, nails, and hair conditions.

Human hair matrix cells and dermal papilla fibroblasts can form early hair follicle structures but don't produce hair shafts yet.

Children with systemic lupus erythematosus have different skin symptoms than adults.

Murine hair has specific types of ceramides and glucosylceramides but lacks acylceramides.

The new gel combining calcipotriene and betamethasone is effective and safe for treating scalp psoriasis.

Scientists found a new protein, AMY117, common in Alzheimer's patients, which could be important for treatment and diagnosis.

Snakes and worm lizards lost claw proteins due to similar evolutionary changes.