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Six new genes linked to early hair loss were found, which also surprisingly connect to Parkinson's disease and lower fertility.

Not having the gene PLAAT3 leads to fat loss, high insulin resistance, and abnormal fat levels in the blood due to a disruption in fat cell development and function.

Two genes, ERBB4 and ROR1, may cause the unique pigmentation in Lanping black-boned sheep.

A mutation in the vitamin D receptor causes severe resistance to vitamin D, affecting bone health but not hair growth.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

Mutations in the hairless gene cause hair loss and skin cysts in rhesus macaques.

Patients with RASopathies have a higher risk of autoimmune disorders and should be routinely screened.

Genetic variation in the KRTAP15-1 gene affects wool yield in sheep.

The A allele of the C2 gene increases the risk of lupus, while the G allele may protect against it.

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

Certain genetic variations in the A2M gene are linked to better milk quality in Murrah buffaloes.

NEDD4 and NEDD4L help control intestinal stem cells and prevent tumors by breaking down the LGR5 receptor.

CARASIL, a rare genetic disorder, was confirmed in an Arabic woman, highlighting its rarity and need for stroke prevention.

Double-stranded RNA helps regenerate hair follicles by increasing retinoic acid production and signaling.

A mutation in the KRT74 gene causes tightly curled hair.

A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

Early-onset hair loss is linked to Parkinson's disease and decreased fertility.

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

A new gene variant causes curly coats in some dog breeds.

Key genes can rewire networks, changing skin appendage types.

Ritlecitinib effectively regrows scalp, eyebrow, and eyelash hair in Asians with alopecia areata and is safe.

AGC2-1 protein is essential for root hair growth in Arabidopsis.

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

Aromatase gene variation may increase female hair loss risk.

Six new genes linked to early hair loss were found, which also surprisingly connect to Parkinson's disease and lower fertility.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

Upadacitinib effectively treats skin conditions like eczema and psoriasis and is becoming more widely used and affordable.

A woman got a skin rash from taking aceclofenac, which went away after she stopped the drug.

RDW can be a useful marker for inflammation in alopecia areata patients.