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A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

Foxi3 expression in developing teeth and hair is controlled by the ectodysplasin pathway.

Disabling the FGF5 gene in sheep leads to longer wool.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

The gene Foxn1 is important for hair growth, and understanding it may lead to new alopecia treatments.

Researchers found genes and genetic variants linked to sheep wool and skin wrinkles.

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

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.

Reducing Tyrosinase prevents mature color pigment cells from forming in mouse hair.

Certain cells in the adult mouse ear come from cranial neural crest cells, but muscle and hair cells do not.

A man with hypoparathyroidism had other health issues that led to a diagnosis of a rare autoimmune disorder, APS-1.

Hair loss in autoimmune blistering skin diseases varies and may regrow with disease control.

FGF5 gene mutations cause long hair in domestic cats.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

DFMO treatment improves hair growth, muscle tone, and development in Bachmann-Bupp syndrome patients.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

Estrogens are key for bone growth spurts in both boys and girls and affect growth into adulthood.

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

Mutations in the androgen receptor gene cause Androgen Insensitivity Syndrome, affecting sexual development.

Changes to the Foxp3 protein affect how well regulatory T cells can control the immune system, which could help treat immune diseases and cancer.

Researchers found two new genetic variants linked to Alzheimer's disease.

The KRTAP21-2 gene affects wool length and quality in sheep.

A male with aromatase deficiency improved bone health with estradiol treatment.

Oestrogens are key for bone growth during puberty in both boys and girls.

A rare gene mutation causes skin fragility and itching without affecting hair or nails.

New biopsy techniques and tools improve alopecia diagnosis, and both too much and too little selenium can cause hair loss.

Alkaline Ceramidase 1 prevents early hair loss in mice by keeping hair follicle stem cells balanced.

A faulty KLHL24 gene leads to hair loss by damaging hair follicle stem cells.