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A new sheep gene, KRTAP36-1, may help breed sheep with better wool by reducing prickle factor.

A gene mutation in mice causes skin defects and early death.

A second domain of high sulfur KAP genes on chromosome 21q23 is crucial for hair structure.

Certain SPINK5 gene mutations are common in Israeli families with Comèl-Netherton syndrome.

A genetic variant in the KRT25 gene causes tightly curled hair.

CaM7 and CNGC14 interaction controls root hair growth in Arabidopsis.

Keratin2-6g is crucial for hair follicle development, with mutations causing cell degeneration and vacuolation.

A new mutation in the mitochondrial DNA was found in a boy with MELAS, even though his family didn't show typical signs.

CDP is crucial for lung and hair follicle cell development.

Nellore cattle have genetic variations linked to their adaptation to tropical environments.

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

The research identified a gene in sheep important for wool quality, which could help improve wool traits.

Certain genetic variants reduce enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

Variants in the CCDC47 gene are linked to trichohepatoneurodevelopmental syndrome.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

The frizzy mouse and hairless rat mutations are due to changes in the Prss8 gene.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

CRISPR/Cas9 and prime editing can potentially fix skin disorder genes safely and effectively.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

CTCF protein is essential for skin and hair follicle development in mice.

Certain genetic variants in PRLR and PCCA genes may lead to shorter hair in cattle, which could help with heat tolerance.

Non-coding RNA boosts retinoic acid production and signaling, aiding regeneration.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

A new ARID1B gene variation causes Coffin-Siris syndrome 1 and early high myopia in a Chinese family.

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.

A new gene mutation causes insulin resistance in a girl and her mother.

Mice hair follicles take in the amino acid cystine.

The study showed that a specific DNA sequence can control gene expression in hair growth areas of mice.