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Hereditary hyperplastic gingivitis in silver foxes may be linked to errors in the MAPK signaling pathway, influenced by androgens.

Basonuclin may help control ribosomal RNA gene activity in skin cells.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

ERG increases SOX9, promoting prostate cancer growth and invasion.

New SRD5A2 variants may disrupt protein function, aiding diagnosis and treatment of related disorders.

A girl with Evans' syndrome had her low platelet count successfully treated with zanubrutinib.

A mutation in the human hairless gene causes alopecia universalis.

Certain long non-coding RNAs in cashmere goats affect hair growth when treated with a specific growth factor.

Patients with certain FoxN1 gene mutations have severe immune issues but normal skin and hair.

Frontal Fibrosing Alopecia is a hair loss condition mainly affecting postmenopausal women, with unclear causes and various clinical patterns.

Two microRNAs affect hair follicle development in sheep by targeting specific genes.

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

Radiofrequency treatment helps rejuvenate skin by boosting collagen and blood vessel growth.

Zebrafish regenerate sensory hair cells through three phases, offering insights for potential mammal applications.

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

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

Affected males are born with ambiguous genitalia, raised as females, but develop male traits at puberty due to enzyme deficiency.

Targeting FGF5 could help treat prostate cancer.

The FOXN1 gene is crucial for developing immune cells and preventing immune disorders.

VEGF and VEGFR-2 genes influence feather maturity, and specific genetic markers can improve chicken breeding.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.

Increasing miR-149 reduces hair follicle stem cell growth and hair development by affecting certain cell growth pathways.

miR-200a reduces goose fibroblast growth by targeting PITX2 in the Wnt pathway.

A unique gene mutation was found in a family with monilethrix.

The scraggly mutation causes hair loss and skin defects in mice.

Mice with the ab gene have abnormal sebaceous gland development, affecting sebum production.

LncRNA018392 helps goat skin cells grow by increasing CSF1R.

Removing a specific gene in certain skin cells causes hair loss on the body by disrupting normal hair development.