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The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.

The G(S) alpha subunit gene may help start hair follicle growth in newborn mice.

Mice without certain skin enzymes have faster hair growth and bigger eye glands.

Angiotensin II is found at higher levels in black sheep skin and may influence coat color.

Androgen receptor inactivation delays skin cancer onset and reduces incidence in mice, with gender differences in susceptibility.

A genetic variant in the KRT25 gene causes tightly curled hair.

A specific gene variant may increase the risk of developing Alopecia Areata.

Iron deficiency causes hair loss by affecting hair differentiation and cycling.

The study concludes that a genetic mutation in TFM mice leads to reduced androgen receptor activity, affecting the body's response to male hormones.

Certain miRNAs are linked to Cashmere goat hair quality.

Pigs without the Hairless gene showed skin and thymus changes, useful for studying human hair disorders.

Mice that can regenerate tissue have cells that pause in the cell cycle, which is important for healing, similar to axolotls.

The LMNA mutation affects skin structure even in asymptomatic carriers.

Adiponectin reduces inflammation and bone loss in joint replacements.

HPV genes in mice improve ear tissue healing by speeding up skin growth and repair.

Aralia continentalis root extract may help with hair growth.

A mouse model for studying scleroderma in chronic graft-versus-host disease was successfully created.

Modulating BMP activity changes the number, size, shape, and type of ectodermal organs.

The Foxn1 gene is essential for normal nail and hair development.

The Foxn1(-/-) phenotype disrupts hair growth and affects skin stem cells.

Knocking out the FGF5 gene in sheep increased wool production and hair-follicle density.

Mutations in claudin-1 and claudin-3 cause hair loss in baby mice.

The prolactin gene polymorphism doesn't affect cashmere quality in these goats.

Defective protein folding due to a mutation is key in ANE syndrome.

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

Researchers found a gene in hamsters that responds to male hormones and may be indirectly controlled by them.

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

Prenatal retinoic acid exposure did not affect mouse vibrissal follicle development.