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Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

SLC24A5 shows a clear selective sweep, but no link to UV radiation intensity.

A genetic hair protein variant is more common in Japanese people and is inherited.

Researchers identified a new variant of the FGF5 gene in sheep that affects hair length.

The Trichodysplasia spinulosa virus protein can cause abnormal hair growth in mice.

CRISPR/Cas9 editing in spinach affects root hair growth by altering specific genes.

PolyQ repeats in neural proteins evolve together, affecting brain function and disease.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

Forensic DNA phenotyping faces challenges due to inconsistent terminology, limited genetic understanding, and debates over technology and models.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

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

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

FGF5 gene mutations cause long hair in domestic cats.

Over-expression of Sp2 can lead to cancer by preventing proper stem cell differentiation.

A new gene mutation linked to a skin condition was found in a Spanish family.

The document concludes that careful design of genetic fate mapping experiments is crucial for accurate cell lineage tracing in mice.

No significant link was found between the studied genes and female hair loss in the Polish population.

Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.

The prolactin gene polymorphism doesn't affect cashmere quality in these goats.

Increasing SSAT makes skin more prone to cancer.

The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.

A patient with a larger than usual genetic mutation had a broader range of symptoms for a muscle disease.

A Japanese patient with IFAP syndrome had a severe MBTPS2 gene mutation but showed milder symptoms than previously observed cases.

New mutations in MBTPS2 reduce its function and cause IFAP syndrome with unusual symptoms.

Certain variations of the HDAC9 gene can increase or decrease stroke risk in the Chinese population.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.