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The gene for Clouston syndrome in a large Indian family is located in the 13q11-q12.1 region.

Roselle flower extracts can protect against free radical damage in UV-irradiated antibiotics.

FGF signaling is a promising target for developing treatments for wounds, metabolic diseases, and cancer.

A new genetic mutation in the hairless gene causes a rare hair loss disorder.

NCBP3, SDHA, and PTPRA are the best genes for normalizing goat skin experiments.

Certain genes may promote longer root hairs in plants when phosphorus is low.

Melatonin receptor genes likely play an important role in the development of goose feather follicles.

Microneedling radiofrequency improves skin texture and tone by stimulating collagen and elastin.

RORA may help regulate hair growth by affecting hair follicle stem cells.

A new gene mutation is linked to monilethrix in the studied family.

A new method helps find proteins in hair to identify fetal growth issues.

Platelet-rich plasma improves skin flap survival by reducing tissue death.

TLR2 is important for hair growth and can be targeted to treat hair loss.

A new method accurately estimates clone sizes in cells without considering time.

EFFC might be common but underreported.

Most people have similar hair protein patterns, but a rare variant was found in two women.

Method accurately measures finasteride and tamsulosin in combined drug form.

Autofluorescence can sort plant cells without labeling.

Lef1 is essential for normal skin, hair growth, and healing wounds in mice.

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

RXR-alpha is strongly expressed in both normal and psoriatic skin and may help in skin cell differentiation and hair growth.

The treatment combining laser and fetal fibroblasts effectively reduces scarring.

The method successfully isolates hair follicle stem cells from mice for research.

IL-1 blockade is effective for treating SURF, and personalized treatment is needed.

Microfluorometry effectively measures how much polymer coats and penetrates hair, useful for evaluating hair products.

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

Mutations in the hairless gene cause a rare form of permanent hair loss.

KAP7.1 and KAP8.2 genes are crucial for cashmere quality in goats.

Long-Acting Platelet Rich Plasma therapy can effectively reduce hair shedding, thicken hair, and promote new growth in women with pattern hair loss.