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The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

KAP9.2 and Hoxc13 genes are important for cashmere growth and vary in activity during different stages.

A new genetic mutation in the TRPV3 gene causes Olmsted-like syndrome in a Mongolian family.

ACKR2 helps prevent skin scarring and hair loss by controlling inflammation.

The study found genetic differences related to hair development that may explain hair loss in a patient with Trichorhinophalangeal syndrome type I.

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

PADI4 enzyme slows down cell growth in developing hair follicles.

A new genetic mutation in mice causes permanent hair loss and skin wrinkling.

TAp63 and NRF2 work together to manage oxidative stress, preventing premature aging and aiding skin functions.

Certain genetic variants in PRLR and PCCA genes may lead to shorter hair in cattle, which could help with heat tolerance.

Certain peptides can prevent hair loss in young rats caused by a cancer drug.

IGFBP-rP1 could be a new treatment for a common type of hair loss.

Genetic mutations linked to ectodermal dysplasias and hair loss were identified in Pakistani families.

The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

Mutations in the P2RY5 gene cause hereditary woolly hair.

People with alopecia areata have higher levels of RBP4 protein and antibodies against it.

Targeting Keratin 17 may help overcome cancer therapy resistance.

Retinoic acid-binding proteins in skin are regulated by β-catenin and Notch signalling.

PX-12 may help treat psoriasis by blocking inflammation and cell death.

The peach gene CTG134 helps control the interaction between auxin and ethylene, which could lead to new agricultural chemicals.

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

CD98hc's role in skin health decreases with age.

Keratin 15 expression in skin cells is regulated by two mechanisms involving PKC/AP-1 and FOXM1.

ESR2 gene linked to female-pattern hair loss.

Deleting Gpr54 speeds up hair growth and regeneration.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

Researchers found a new mutation causing total hair loss from birth.

FCER1A and RGS1 may help diagnose and treat systemic lupus erythematosus.