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

Scientists found a new gene in a bacterium that can modify an immunosuppressant drug, potentially helping to treat hair loss.

A new gene causes hairlessness and skin cysts in rats.

One minoxidil-sensitive potassium channel exists in human hair follicles.

Targeting mitophagy may help treat alopecia areata by reducing inflammasome activation.

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

Genetic analysis is crucial for diagnosing and managing cerebral arteriopathy.

The study concluded that specific proteins are necessary to maintain the structure that holds epithelial cells tightly together.

EDA2R gene linked to hair loss.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

A mutation in the KRT74 gene causes woolly hair by affecting hair texture.

A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

Mitochondrial genes help predict breast cancer outcomes and spread.

The guidelines ensure accurate genetic testing and reporting for 21-hydroxylase deficiency.

Mrp3 may aid in wound healing and hair growth.

The hairless gene is crucial for hair health, and its mutations cause hair loss.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

The same gene mutation can cause different symptoms in family members.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

CaM7 and CNGC14 interaction controls root hair growth in Arabidopsis.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

KRT14 gene variants cause dermatopathia pigmentosa reticularis, affecting nails, teeth, and hair.

Prenatal genetic diagnosis may not predict MELAS syndrome severity in offspring.

AR/EDA2R gene linked to early-onset female hair loss, but 20p11 gene not involved.

The TGM3 gene's promoter region is key for skin and hair cell function and may aid gene therapy.

Four genes are potential markers for hair loss condition alopecia areata, linked to a specific type of cell death.

Mrp3 helps in wound healing and hair growth.

Researchers identified genes in scalp hair follicles that may affect hair traits and hair loss.

Two new mutations in the AR gene linked to severe androgen insensitivity were found.