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The wavy coat in NCT mice is caused by multiple genes, including a mutation in the Prss53 gene.

KRT2.13 gene is similar to KRT2.9 but not expressed in hair follicles.

Different keratins have unique expression patterns in mouse skin cells.

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

Small molecules KY19382 and KY19334 may help treat skin cancer by reducing CDK1 levels and blocking harmful cell signals.

Nexin 1 may help control hair growth.

lncRNA2919 slows down rabbit hair growth by stopping cell growth and causing cell death.

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

Mutations in the WNT10A gene can cause skin, hair, teeth, and other disorders, and may also affect other areas like kidney and cancer, with potential for targeted treatments.

WNT10A gene mutations cause short anagen hair syndrome.

The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.

A new gene variant causes curly coats in some dog breeds.

CXXC5 is a protein that controls cell growth and healing processes, and changes in its activity can lead to diseases like cancer and hair loss.

Deleting the CDSN gene causes severe skin and hair problems, leading to death.

Clouston syndrome is inherited in an autosomal dominant pattern and caused by a specific gene mutation, with no current treatment available.

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

A genetic mutation in the CDH3 gene causes hair loss and vision problems in a young Saudi girl.

A new test helps find drugs to treat head and neck cancer by targeting c-Rel.

Steroid hormones may affect sexual maturation in cod by altering certain KCa channel expressions.

Four keratin genes are crucial for hair growth in Xinji fine wool sheep.

Jumonji genes are important for development and their mutations can cause abnormalities, especially in the heart and brain.

A rare gene variant causes hair and nail issues in a family.

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

Non-coding RNAs may be key in diagnosing and treating rare skin disorders.

A boy with a new NR5A1 gene mutation has a sex development disorder without affecting his adrenal glands.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

TSC22D genes are key in metabolic diseases and cancer, offering potential as treatment targets.