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The study concluded that three enzymes are important for plant development by affecting sugar composition and calcium binding in plants.

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

A cat's poor wound healing was linked to a genetic deletion in the COL5A1 gene.

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

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

CT60 polymorphism might increase the risk of Alopecia Areata.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

Cats with abnormal hair had DSG4 gene changes causing hair problems.

Cathepsin L deficiency causes large, abnormal cell structures and health issues in mice.

Hair-follicle nerves in cats' spinal cords can be inhibited by GABA-related connections.

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

Cystatin M/E strongly inhibits cathepsin V and cathepsin L, important for skin formation.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.

The rhg mutation in mice affects the Oat gene, causing hair growth issues and other symptoms.

The wavy coat in NCT mice is caused by multiple genes, including a mutation in the Prss53 gene.

MPA increases cancer spread by boosting Eph A2 activity.

α- and γ-catenins help develop fetal skin by 23 weeks.

pCLCA2 protein may help maintain skin structure and function.

Cathepsin L deficiency causes hair and skin issues in mice.

Mouse and human keratin 16 can both form filaments, with differences likely due to the tail domain, not the helical domain.

The HGCA tool helps identify genes that work together by analyzing their co-expression patterns.

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.

The study found that variations in hair protein genes are likely due to evolutionary deletions or duplications.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

Presynaptic inhibition of certain nerve fibers in cats is mainly controlled by GABA and glycine.

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

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

Activating β-catenin in different skin stem cells causes various types of hair growth and skin tumors.