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Certain gene mutations in Japanese people are linked to different types of hair loss, with some causing mild hair thinning and others leading to complete baldness.

Mutations in the enzyme don't significantly change how it binds to its specific substances.

A new genetic mutation linked to Hutchinson-Gilford progeria syndrome was found in China.

Adrenomedullin 2 stops cell growth and causes cell death in human hair follicles.

Pygopus 2 helps ovarian cancer cells grow by aiding ribosomal RNA production, independent of Wnt signaling.

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

Mouse models help study genetic skin diseases.

Vitamin D receptor can control the hairless gene linked to hair loss even without vitamin D.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

Giving a special protein to dogs with a certain genetic disease improved their symptoms but didn't help with hair growth.

RHUPUS should be considered in children with deforming arthritis.

A specific gene mutation causes a severe skin disorder in a family.

Hairless protein can block vitamin D activation in skin cells.

Normal skin cell renewal doesn't need RAR signaling, but vitamin A-related skin thickening does.

The balance between cell renewal and differentiation controls the growth of cancerous cells in mouse skin.

Two new gene mutations cause a rare hair disorder.

A child with a rare vitamin D-resistant condition improved with treatment.

Specific keratin gene mutations can cause monilethrix.

A mutation in the MAP2 gene causes reduced hair follicle density, leading to hairlessness.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

A new genetic mutation in the hairless gene causes a rare hair loss disorder.

An 8-year-old boy with Recklinghausen's Disease shows various symptoms and is from a family with close genetic ties.

A new mutation in the ST14 gene was found in a patient with ARIH syndrome, showing milder symptoms and no tooth issues.

MPZL3 is crucial for seborrheic dermatitis development.

A new mutation, Glu402Lys, in hair keratin is linked to variable symptoms of monilethrix.

Rhupus is a complex syndrome that combines rheumatoid arthritis and lupus, making diagnosis challenging.

High levels of ODC and a mutant Ha-ras gene cause tumors in mice.

Removing a specific gene in certain skin cells causes hair loss in mice by disrupting hair follicle development.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

HSD11b1 affects skin nerves and increases non-histaminergic itch.