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Lymphoid-specific helicase (Lsh) is crucial for skin growth, change, and healing after injury.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

FCER1A and RGS1 may help diagnose and treat systemic lupus erythematosus.

FTase and GGTase-I are essential for skin keratinocyte health.

TCF/Lef1 activity is essential for proper skin cell development and renewal.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

The TG5 gene affects beef cattle weight, and the CC genotype leads to higher weights.

TAF4 is important for skin cell growth and helps prevent skin cancer in mice.

Researchers created human hair follicles using a new method that could help treat hair loss.

HFMs can help study hair growth and test potential hair growth drugs.

Mouse high-glycine/tyrosine proteins have distinct patterns in hair follicles, peaking at specific hair cycle days.

Rat hair follicle stem cells can be used to improve blood vessel growth in engineered skin.

Human hair follicle stem cells can be turned into red blood cells.

Genetic marker rs12558842 strongly linked to male hair loss.

A specific gene change is linked to severe hair loss.

Lhx2 helps retinal cells respond to signals for eye development.

Enhancing CD8+ T cell function to induce ferroptosis in tumor cells may help treat skin melanoma.

Generalized hair follicle hamartoma can occur with systemic lupus erythematosus.

The Foxn1(-/-) nude mouse shows disrupted and expanded skin stem cell areas due to high Lhx2 levels.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

A point mutation in the androgen receptor gene causes complete androgen insensitivity.

Higher PHGDH levels cause unusual melanin buildup in hair follicles.

K6 gene expression can be controlled and manipulated in mice for studying skin disorders.

Mutations in the vitamin D receptor cause hereditary vitamin D-resistant rickets, leading to poor bone health and requiring high calcium doses for treatment.

The FDA approved the first gene therapy for a blood disorder after overcoming early challenges and demonstrating patient benefits.

An infant with Hutchinson-Gilford Progeria Syndrome had successful surgery to fix breathing issues caused by a new genetic mutation.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

An mFG score of 5 or more indicates above-normal hair growth in Southern Chinese women.