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A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

LONRF1 is important for oxidative damage response and tissue remodeling during wound healing.

Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.

A mutation in the VDR gene affects hair cycling without needing ligand binding.

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

Four-amino acid part makes enzyme sensitive to finasteride.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

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

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

A new method helps diagnose alopecia areata using specific gene markers and could guide targeted treatments.

Non-coding RNA boosts retinoic acid production and signaling, aiding regeneration.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

HLA-DRB5 and other genes may be linked to alopecia universalis.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

CLE40 and CRN/CLV2 pathways have opposite effects on root growth in Arabidopsis.

Hair loss gene linked to prostate issues.

EDA and EDAR are important for hair follicle development in cashmere goats and affect other related genes.

A protein called sFRP4 from skin cells stops the development of pigment-producing cells in hair.

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

The research suggests that a specific skin gene can be controlled by signals within and between cells and is wrongly activated in certain skin diseases.

ANE syndrome is caused by a mutation in the RBM28 protein that disrupts ribosome assembly.

Two new mutations in the AR gene linked to severe androgen insensitivity were found.

KLF4 is important for maintaining stem cells and has potential in cancer treatment and wound healing.

Genetic variants at 20p11 increase baldness risk in Chinese Han people.

Certain genes may promote longer root hairs in plants when phosphorus is low.

The LTF gene may help predict and manage nonspecific orbital inflammation.

AtVPS29 is essential for proper plant growth by regulating gibberellin signaling.