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The specific skin disease variant p.(Arg2000Trp) in plectin can cause a wide range of symptoms, which should be considered when diagnosing patients.

61 functional keratin genes were identified in dogs and horses, leading to updated gene annotations.

CRABP2 helps increase the growth of cells important for hair growth by activating a specific growth pathway.

TSC22D genes are key in metabolic diseases and cancer, offering potential as treatment targets.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

DNAJB9 cfRNA could help diagnose and treat female hair loss.

Removing the ATR gene in adult mice causes rapid aging and stem cell loss.

A specific gene change is linked to severe hair loss.

A genetic mutation in the LIPH gene causes a rare hair disorder with sparse, curly hair.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

A certain mutation in the fetal alpha 5-reductase gene is linked to a higher risk of late miscarriage.

Compound 7p shows strong potential as an anticancer agent.

A severe form of Netherton syndrome caused by a specific gene mutation led to neonatal deaths in a family.

miR-200c-3p could help diagnose and treat alopecia areata.

Congenital atrichia with papular lesions causes permanent hair loss and skin bumps due to a gene mutation.

Longer TA repeats in the SRD5A2 gene may increase acne risk in Chinese people.

Inhibiting connective tissue sheath contraction may improve hair growth in male pattern baldness.

No link found between aromatase gene and female hair loss.

A new EDA gene variant causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family.

Epilation and DHT cause skin calcification by increasing ATP and calcium deposits.

New biological pathways and potential treatment targets for male pattern baldness were identified.

Blood tests for tumor cells could improve prostate cancer diagnosis and treatment; hair loss severity linked to a gene affecting prostate conditions.

Patients with the same vitamin D receptor mutation showed different symptoms due to other factors.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

Skin cells from people with Epidermolysis Bullosa Simplex have abnormally placed and less active mitochondria.

KAP8.2 gene variations affect cashmere quality in goats.

Type I keratin genes are closely linked to the rex locus on mouse chromosome 11, affecting hair development.

Hairless gene not strongly linked to baldness.

The testes significantly contribute to vitamin D metabolism and may affect male reproductive health and conditions like hair loss.