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N6-methyladenosine affects hair follicle development differently in Rex and Hycole rabbits.

Removing REDD1 in mice increases skin fat by making fat cells larger and more numerous.

Targeting NCoR1 can help treat heart enlargement and dysfunction.

Researchers found genes that affect hair growth in Yangtze River Delta white goats.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

A rare gene variant causes sexual development issues in siblings, needing personalized treatment.

Wnt10b can help regenerate hair follicles.

OsPHR3 can help breed rice that efficiently uses phosphate without growth issues.

PNKP is essential for keeping adult mouse progenitor cells healthy and growing normally.

Pannexin 3 helps skin and hair growth by controlling a protein called Epiprofin.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.

A soluble factor in developing mouse whisker pads boosts nerve growth factor mRNA production.

Walnut extract may help lower cholesterol and inflammation.

The protein called small nuclear ribonucleoprotein polypeptide E is identified as a cause of a type of hair loss without other symptoms.

Trps1 plays a key role in hair follicle development and cycling.

NCSTN gene mutation causes abnormal skin cell differentiation and more inflammation, contributing to Hidradenitis Suppurativa.

RAR-gamma 1 is important for normal skin maintenance and differentiation.

DNA changes in tetraploid wheat improve root growth and nitrogen use.

A point mutation in the androgen receptor gene causes complete androgen insensitivity.

A prostate cancer drug can lower the levels of a protein that the coronavirus uses to enter lung cells.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

Dkk4 protein is necessary for the proper development and arrangement of hair follicles.

A gene variation is linked to hair thickness in Asians.

RORA affects hair follicle stem cells' structure and movement, potentially helping treat hair loss.

LED light helps human hair root cells grow and move by activating certain cell pathways.

Three new gene mutations cause rickets and hair loss, treatable with high calcium and calcidol, but hair regrowth is rare.

Three siblings with a genetic form of rickets showed different symptoms of the disease.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

Zfp157 is active in many mouse tissues during development and in specific adult cells.

Enzyme purified and characterized for minoxidil sulphation in rat liver.