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The PTGER2 gene is highly active in Cashmere goat skin and its activity changes with the hair growth cycle.

The G allele of IFITM3 rs12252 is linked to more severe COVID-19.

Certain genetic variations are linked to hair loss in Mexican men.

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

A young patient with unusual insulin resistance and high testosterone levels had a rare INSR gene mutation.

Promising cancer treatments were found, but the manufacturer closed.

The ABHRS held a test in Capri, Italy.

SFRP2 and PTGDS may be key factors in female hair loss.

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A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

Mutations in the ACTB gene cause Becker’s nevi and may lead to muscle issues in Becker’s nevus syndrome.

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Mutations in the hHb6 gene cause the hair disorder monilethrix.

Finasteride helps female-pattern hair loss.

Certain genetic variations in camels affect hair coarseness.

Four new genes related to sheep wool were discovered, showing genetic diversity.

Two siblings were found to have a genetic condition causing progressive hair loss and woolly hair, which may often be misdiagnosed.

Microarray analysis helps find hidden chromosomal changes in patients with intellectual disabilities and birth defects.

Certain genetic markers may increase or decrease prostate cancer risk.

The DMI3 gene is essential for nodule development and symbiosis in certain plants.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.

Genetic mutations linked to ectodermal dysplasias and hair loss were identified in Pakistani families.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

ROOT HAIR SPECIFIC 10 (RHS10) reduces the length of root hairs in Arabidopsis plants.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

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A new mutation in the KRT86 gene causes a hair disorder with variable expression.