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The protein RSL4 is crucial for making root hairs longer by controlling genes related to cell growth.

Variation in the TCHH gene affects wool curliness in sheep.

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

Truncated hHb1 keratin may play a role in breast cancer cell transformation.

IL-4 gene variation may increase the risk of alopecia areata in Turkish people.

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

Researchers found a new gene area linked to male-pattern baldness, which, along with another gene, significantly increases the risk of hair loss in men.

Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

Methylated gene parts may cause finasteride-resistance in some enlarged prostate patients.

Researchers found two new genetic variants linked to Alzheimer's disease.

AR-27 E-Chol siRNA can effectively promote hair regrowth for androgenetic alopecia.

Hirosaki hairless rats lack hair due to missing DNA with key keratin genes.

The L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.

A specific gene variant (rs4833095) is linked to a higher risk of alopecia areata in Koreans.

A keratin hHb6 mutation causes a hair disorder with varying severity, influenced by other factors.

The hHa7 gene is regulated by androgens in certain body hair, not scalp hair.

Hair pattern in androgenetic alopecia overlaps with scalp and bone demarcations, with distinct gene profiles affecting susceptibility.

Certain gene variations might increase the risk of a hair loss condition in Koreans.

Two enzymes regulate androgen receptor activity, affecting treatments for androgen insufficiency and benign prostatic hyperplasia.

A new gene mutation causes female pseudohermaphroditism due to glucocorticoid resistance.

Certain genetic markers can indicate higher or lower risk for systemic lupus erythematosus.

The Arabidopsis rhd2 mutant is more sensitive to drought because of changes in cell membrane proteins and cell structure.

Certain genes on chromosomes 6, 10, 16, and 18 may increase the risk of alopecia areata.

Hair root sheaths can be used to accurately analyze genetic markers.

A protein called ectodysplasin-A2 increases a hair growth inhibitor in balding cells, which could be a target for hair loss treatment.

The E413K mutation in the hHb6 gene causes monilethrix, a hair disorder, but doesn't show consistent symptoms.

KRT72 gene helps form hair.

Researchers found four genes that could help diagnose severe alopecia areata early.

Researchers found certain genes are overactive and others are underactive in men with early balding, which could help create new treatments.