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Certain long non-coding RNAs in cashmere goats affect hair growth when treated with a specific growth factor.

Laminin-511 is involved in psoriasis development and can be regulated by cannabinoid receptor type 1.

The mutated hairless gene causes hair loss by acting as a new type of corepressor affecting thyroid hormone receptors.

Adding TERT and BMI1 to certain skin cells can improve their ability to create hair follicles in mice.

miR-203a-3p helps hair follicle stem cells become specialized by targeting Smad1.

Tofacitinib helps mice grow more hair by increasing noggin and BMP4 levels, possibly better than minoxidil.

Tofacitinib helped most teenagers in the study regrow hair with mild side effects.

Rac1 is essential for proper hair structure and color.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

The Wave complex controls skin growth by suppressing certain signals.

Restoring hair follicle immune privilege may help treat alopecia areata.

The hairless (hr) gene is essential for normal hair follicle function and its mutation leads to hair loss.

Brg1 is crucial for keeping hair follicle stem cells and repairing skin, working with the Sonic Hedgehog pathway to promote hair growth.

New mutations in MBTPS2 reduce its function and cause IFAP syndrome with unusual symptoms.

A specific gene mutation causes congenital hair loss.

Overexpression of hurpin in mice leads to abnormal skin and higher skin cancer risk.

A specific RNA increases hair stem cell growth and skin healing by affecting a protein through interaction with a microRNA.

Collagen XXII is a marker for tissue junctions, aiding in structural integrity and found in muscles, heart, skin, and arthritic joints.

Birt–Hogg–Dubé syndrome is a rare genetic condition causing skin lesions, lung cysts, and a higher chance of kidney cancer.

Certain gene mutations in Japanese people are linked to different types of hair loss, with some causing mild hair thinning and others leading to complete baldness.

AGC2-1 protein is essential for root hair growth in Arabidopsis.

A new mutation in mice causes crooked whiskers and messy hair.

A mutation in the Adam10 gene causes freckle-like spots on Hairless mice.

The ovine Hoxc-13 gene is crucial for hair formation and may have other skin functions.

Frontal fibrosing alopecia is linked to increased immune system activity and reduced stem cells, suggesting early treatment targeting this pathway might prevent hair follicle damage.

Intermediate filaments are crucial for cell differentiation and stem cell function.

The study provides exploratory findings on miRNA changes in female hair loss.

Farudodstat may effectively treat alopecia areata without harming hair follicles.

miRNAs in the Dlk1-Gtl2 region may improve lamb fur quality.

Human growth factor 20 can boost mouse whisker growth.