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The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

Hedgehog signaling controls hair follicle development and can affect skin cancer growth.

Id2 gene helps keep hair follicle stem cells inactive.

A Turkish woman has a hair condition caused by a LIPH gene mutation.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

The study found two new mutations in a Chinese patient with severe biotinidase deficiency.

The SNP rs6457452 is linked to a higher risk of alopecia areata in Koreans.

A specific gene mutation causes complete hair loss in an Irish Traveller family.

Knockout mice showed anemia and hair loss, suggesting other ways exist for iron absorption.

Hoxc8 gene helps start mammary gland development by controlling specific signals.

The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.

A genetic mutation in the CDH3 gene causes hair loss and vision problems in a young Saudi girl.

A mutation in the iRhom2 gene causes hairless mice due to abnormal hair follicle development.

A new keratin 6 type in mice explains why some mice without certain keratin genes still have normal hair and nails.

Brg1 is crucial for hair growth and skin repair by maintaining stem cells and promoting regeneration.

K6hf is a unique protein found only in a specific layer of hair follicles.

The HCR gene contributes to psoriasis risk.

Bcl-2 affects hair growth and pigmentation by controlling cell death.

Faulty LEF1 activation causes faster skin cell differentiation in premature aging syndrome.

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

Mutant MK6a transgenes in mice cause blistering, hair loss, and potential human alopecia.

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

A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

The hairless gene mutation causes baldness by disrupting hair follicle structure.

A deletion in the CDH3 gene causes a rare disorder with short hair and vision loss.

Different Hairless isoforms affect Vitamin D receptor activity in hair regulation, with one repressing and the other stimulating it.

HSD11b1 affects skin nerves and increases non-histaminergic itch.