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A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

KGF and its receptor are found in enlarged prostate tissue and KGF strongly increases cell growth.

A new hydrogel with stem cells from the human umbilical cord speeds up healing in diabetic wounds.

People with Mucopolysaccharidoses often have skin problems like thick skin and extra hair, and recognizing these can help diagnose and treat the condition early.

Urtica dioica extract may help treat androgenic skin diseases by reducing a specific gene's activity.

A specific gene variation increases the risk of high uric acid and cholesterol in young Mexican males.

Goserelin injections can effectively manage hyperandrogenism symptoms in postmenopausal women who can't have surgery.

Corneodesmosin is essential for skin and hair health, and its dysfunction can lead to skin and hair disorders.

Urotensin II increases growth and VEGF production in rat skin cells by turning on the Wnt-β-catenin pathway.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

MsPG3 protein gathers at root hair tips, aiding growth.

Cats with abnormal hair had DSG4 gene changes causing hair problems.

The curly mutation in SELH/Bc mice affects hair and may help study human genetic disorders.

The new anti-acne treatment HA-P5 effectively reduces acne by targeting two key receptors and avoids an enzyme that can hinder treatment.

A 4kb fragment of the desmocollin 3 promoter targets gene expression to specific skin and hair follicle areas.

Glycerol is essential for skin hydration in mice without sebaceous glands.

Researchers created human cells that can turn into sebocytes, which may help study and treat skin conditions like acne.

Certain enzymes react strongly with some hormones in rat skin during hair growth, mainly in sebaceous glands and hair sheaths.

Women with non-classical congenital adrenal hyperplasia have higher levels of certain steroids, which can be reduced by treatment.

Y27632 increases cell growth through EGFR signaling, not ROCK1/2.

The enzyme sEH is important for hair growth and its inhibition could help treat hair loss.

A boy with progeria had eye problems and signs of aging like hair loss and skin wrinkling.

LGR5 is a marker found in hair follicle stem cells in various species and is important for hair growth and skin repair.

Growth hormone is important for regulating human hair growth.

A genetic mutation in a specific gene causes a salt-wasting condition in a Pakistani girl and her family.

A certain genetic variation is linked to a higher risk of polycystic ovarian syndrome.

EGFR inhibitors can cause unusual localized hair growth.

A new gene mutation causes a rare type of hair loss.

Drugs that block GSK-3 show promise for treating various diseases.