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

A genetic variant in the KRT71 gene may cause loose anagen hair and wooly hair, and symptoms might improve with age.

VDR gene variations may affect carbohydrate metabolism in young women with hyperandrogenism.

Genetic testing is crucial for diagnosing rare hair loss disorders.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

Mutations in mitochondrial DNA might significantly contribute to the development of Polycystic Ovarian Syndrome.

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

Researchers made a mouse model with curly hair and hair loss by editing a gene.

STK11 gene variations do not predict how well metformin will work for PCOS, but may affect hair loss and excess hair growth.

Certain gene mutations can weaken the skin barrier and, when combined with environmental factors, lead to eczema and severe itching.

Female pattern hair loss is different from male pattern hair loss and has unclear genetic causes.

Keratin mutations may cause scarring alopecia by damaging hair structure.

Histone demethylases can change gene expression and may be linked to diseases like cancer.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Scientists found a gene in mice that causes early hearing loss.

Basal cell carcinomas and squamous cell carcinomas have different gene activity patterns, suggesting unique treatment approaches.

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

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

Disrupting the FGF5 gene in rabbits leads to longer hair by extending the hair growth phase.

A mutation in the Adam10 gene causes freckle-like spots on Hairless mice.

Mice with a Gsdma3 gene mutation have thicker skin and longer hair follicle openings due to increased β-catenin levels.

Overexpression of HDGF in melanocytes does not cause cancer.

Thyroid and skin autoimmune diseases share genetic and immune links, affecting both tissues.

Deleting the PTEN gene in mice causes nerve cells to grow larger and heal better after injury, but may cause overgrowth and hair loss in older mice.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

Yeast-derived vesicles can improve hair follicle health and promote hair growth.

Aire mutation reduces alopecia areata, while Notch4 mutation prevents it in mice.

A new EDA gene variant causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family.

Genetic analysis of rabbits identified key genes for traits like coat color, body size, and fertility.

The research shows that a gene called Wnt3 affects hair growth and structure, causing short hair and balding when overactive.