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Mutations in the AP1B1 gene cause a new syndrome with skin, hearing, and developmental issues.

CRH causes hair loss by reducing cell survival in hair follicles.

Foxc1 helps keep hair follicle stem cells inactive, preventing hair loss.

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

The L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.

Rapamycin treatment helps with mitochondrial disease by reducing PKC levels.

Certain miRNAs are linked to Cashmere goat hair quality.

Liposomes show promise for delivering CRISPR for gene editing but face challenges like delivery efficiency and safety concerns.

MCPIP1 in myeloid cells is important for skin cancer development and healthy hair growth.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

Miz1 is essential for proper hair structure and growth.

GPRC5D is linked to the formation of hair, nails, and certain tongue areas.

Activating Nrf2 in skin cells causes skin disease similar to chloracne in mice.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

The method successfully created stable transfection donor cells for goat hair follicle research.

A specific RNA modification in cashmere goats helps activate hair growth-related stem cells.

miRNA-211 reduces melanin in Cashmere goats by suppressing AP1S2.

SSAT is a key enzyme affecting cell growth and metabolism, with potential but risky use in disease treatment.

FOXN1 is crucial for thymus development and immune response in Xenopus laevis.

The frizzy mouse and hairless rat mutations are due to changes in the Prss8 gene.

High glycine–tyrosine keratin-associated proteins help make hair strong and maintain its shape.

BLTP1 and KIF27 gene mutations can help breed better wool sheep.

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

The N gene affects the protein makeup of mouse hair.

Caspase-1 helps hair stem cells move to heal wounded or inflamed skin.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

Foxn1 gene regulation is crucial for thymus development but not for hair growth.

Collagen peptides may boost skin and hair-related gene expression.

Hair growth-related cells need the enzyme SCD1 to help maintain the area that supports hair growth.