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A new mouse gene, Keratin 17n, is mainly found in nail tissue and may explain why mice without Keratin 17 don't have nail issues.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

DNA changes in tetraploid wheat improve root growth and nitrogen use.

SCD1 is crucial for skin health and overall energy balance.

Biotin and biotinidase are essential to prevent health issues, and deficiencies require lifelong supplementation.

Fgfr2b helps maintain healthy skin and prevent cancer.

Key genes and factors crucial for hair follicle development and wool traits in Merino sheep were identified.

Epiprofin helps cells grow in developing teeth, hair, and limbs.

Chinese domestic goats have unique genetic traits due to domestication and geographic isolation.

Lykoi cats' unique sparse hair is linked to specific genetic variants in the Hairless gene.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

TMPRSS2 helps viruses enter cells and protects the prostate from inflammation-related cancer.

Mice without certain skin enzymes have faster hair growth and bigger eye glands.

A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

Noncoding RNAs help determine cashmere quality in goats.

Inherited color dilution in rabbits is linked to DNA methylation changes.

FGF10 and non-coding RNAs are important for cashmere goat hair follicle development.

LncRNAs play a crucial role in muscle regulation and could help develop treatments for Duchenne muscular dystrophy.

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

KAP genes show significant genetic variability, but its impact on hair traits is unclear.

Male mice with FGF5 mutations grow longer hair than females.

The GG genotype of the KRT71 gene leads to longer wool in Gansu alpine fine-wool sheep.

A protein from fat-derived stem cells, DKK1, is linked to hair loss and blocking it may help treat alopecia areata.

Lhx2 is essential for effective Sonic Hedgehog signaling in early retinal development.

Agouti and AGRP affect pigmentation and obesity, with implications for metabolic disorders.

Certain genetic variants increase the risk of aggressive prostate cancer.

The gene for Marie Unna hereditary hypotrichosis is located on chromosome 8p21.

The gene for Marie Unna hereditary hypotrichosis is located on chromosome 8p21, near the hairless gene.

A mutation in the human hairless gene causes alopecia universalis.

Too much Sonic Hedgehog protein stops hair growth in embryos.