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Overexpression of COX-2 causes early hair loss in mice, but can be prevented with a COX-2 inhibitor.

Crossbreeding certain European cattle breeds may cause hair and physical issues in cattle.

A new gene mutation causes vitamin D resistance and hair loss in two unrelated girls.

A mutation in the vitamin D receptor causes severe resistance to vitamin D, affecting bone health but not hair growth.

Monilethrix is linked to a gene cluster on chromosome 12.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

The absence of functional sebaceous glands causes hair follicle destruction and scarring alopecia.

Rodent spiny hair traits are due to genetic factors other than the Edar gene.

The technique successfully promoted hair growth and skin renewal in mice.

Chicken feather gene mutation helps understand human hair disorders.

New genetic variants linked to albinism were found in Pakistani families.

Loss of Desmocollin 3 in mice causes skin blisters and hair loss.

Certain genetic markers linked to wool quality in Rambouillet sheep were identified, which can guide better breeding choices.

Genetic variation in the KRTAP15-1 gene affects wool yield in sheep.

A young Persian cat had a skin infection and low platelets, treated with various medications.

Researchers found genes for cysteine-rich proteins that form the protective layer of hair in humans and sheep.

Certain gene variations are found in people with polycystic ovary syndrome.

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

Different androgen concentrations affect wool-related gene expression differently in Hetian and Karakul sheep breeds.

Follicular vitiligo causes hair to gray without skin color loss.

Uncombable hair is inherited dominantly with complete penetrance.

VEGF and microvessel density are closely linked and peak during specific hair growth phases in cashmere goats.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

A specific gene mutation causes complete hair loss without other health issues.

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

Woolly hair is a rare genetic condition with no effective treatments.

Hoxc13 gene expression and skin thickness change similarly during cashmere goat hair follicle development.

Hairless mice lack fur due to a genetic mutation affecting skin response, not hormone issues.

Certain genetic changes in the KRT82 gene may cause patchy skin in New Zealand rabbits.