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Removing anthrax toxin receptor 1 in pigs prevents Senecavirus A infection and causes a rare disease similar to GAPO syndrome.

Smad1 and Smad5 are essential for hair follicle development and stem cell sleepiness.

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

Mouse Scube3 affects teeth, tongue, vibrissae, and eye development, but not facial structure or limb growth.

Early over-expression of FoxN1 harms immune and skin development.

Fetuin A may increase collagen production and promote scarring.

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

Rac1 is essential for proper hair structure and color.

Skin cells can naturally limit the growth of cancerous changes by balancing cell renewal and differentiation.

A missing mK6irs1 gene causes hair loss in mice.

Hoxc8 gene helps start mammary gland development by controlling specific signals.

MOF controls key genes for skin development by regulating mitochondrial and ciliary functions.

Introducing the rat OTC gene normalized hair growth in SPF-ASH mice.

The study found nine new hair protein genes in human hair follicles.

Removing β-catenin in certain stem cells causes hair whitening and pigmentation issues.

FP-1 is a key protein in rat hair growth, active only during the growth phase.

5α-reduced neurosteroids may help regulate glial cell differentiation.

The hairless mutant gene causes early hair loss and affects skin and thymus development in mice.

The Enriched-GF method efficiently produces high-yield growth factors for tissue repair.

Sheep cells were successfully modified to include a spider silk protein gene.

Oral difelikefalin significantly reduces itch in notalgia paresthetica.

miR-3606-3p reduces skin fibrosis by blocking key signaling pathways.

High LGR5 levels in glioblastoma indicate poor prognosis and are essential for cancer stem cell survival.

Nuclear Factor I-C is important for controlling hair growth by affecting the TGF-β1 pathway.

Deleting the Hoxc13 gene in frogs shows its crucial role in developing skin structures similar to hair.

Specific mutations in a receptor cause facial abnormalities and hair loss.

The study found that males with KFSD had severe skin and eye symptoms, while female carriers had milder symptoms.

Deleting Snai2 and Snai3 causes fatal autoimmunity.

Human hair keratins K85 and K35 create unique filament patterns important for early hair formation.

Scientists restored fertility in male mice lacking a key fertility gene by using a modified gene.