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A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

Mutations in the Sgk3 gene cause fuzzy hair in mice.

A mutation in the KRT75 gene causes frizzle feathers in chickens.

Hoxc13 gene is essential for hair, nail, and papilla development.

Mutations in the Whn gene affect hair keratin gene expression differently.

FGF-5 promotes Cashmere goat hair growth by increasing keratin genes and reducing certain LncRNA and target genes.

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

Nelfb is crucial for forming skin fat tissue by regulating genes needed for fat cell development.

The Celsr1 gene is crucial for normal hair patterning in mice.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

Mutant MK6a transgenes in mice cause blistering, hair loss, and potential human alopecia.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Laminin α5 is essential for skin communication and health.

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

Nails are essential for fingertip regeneration.

Female mice with disrupted 5α-reductase 1 had significant metabolic issues, including stress response problems, insulin resistance, liver fat buildup, and obesity.

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

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

A protein made in a plant stopped hair growth in mice.

High levels of the protein Flightless I worsen ulcerative colitis symptoms in mice.

Mice without the Sp6 gene have problems developing several body parts, including hair, teeth, limbs, and lungs.

High testosterone levels can harm fertility by disrupting the LIF signaling pathway in the uterus.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

FERONIA and LRX proteins help control cell growth in plants by regulating vacuole expansion.

Folliculin helps regulate energy and nutrient sensing, impacting Birt–Hogg–Dubé syndrome.

Deleting Rac1 in the skin depletes stem cells and damages hair follicles.

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

Desmocollin 1 is essential for strong skin and proper skin function.