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Using existing drugs for new purposes could be a cost-effective way to treat chest pain and non-clogged heart arteries, with some drugs for lung blood pressure showing promise but needing more testing.

Astrotactin-2 is cleaved in a specific way that helps understand its maturation.

The study developed a mouse model for Alopecia Areata that responds to treatment, useful for future research.

ACA from Alpinia galanga may prevent testosterone-related hair loss.

Ectopic acanthosis nigricans can occur at surgical sites due to skin graft mismatches.

Dietary L-serine supplementation can reduce symptoms of HSAN1 by lowering harmful 1-deoxySL levels.

Key genes and pathways improve wool quality in Zhexi Angora rabbits.

A KRT32 gene variant causes loose anagen hair syndrome.

The peach gene pCTG134 helps control the interaction between auxin and ethylene hormones during fruit ripening.

mEphA1 receptor tyrosine kinase is important for skin and hair development and may play a role in certain diseases.

There is no significant link between the MMP-1 rs1799750 polymorphism and androgenetic alopecia in the Indonesian population.

Stress can cause a type of hair loss in mice lacking the CCHCR1 gene.

Activating androgen receptors in muscle can increase muscle mass and reduce fat.

A certain genetic variation in the IL1A gene may lower the risk of a hair loss condition in Chinese people.

Targeting the TNFRSF1B gene may help treat hair loss.

Disrupting Acvr1b in mice causes severe hair loss and thicker skin.

Anwuligan may help treat hair loss by promoting hair growth.

Lower MC2R expression may contribute to alopecia areata.

CD8A and FOXD2-AS1 may be key for diagnosing and treating alopecia areata.

Darkened knuckles can be an early sign of insulin resistance.

Certain gene variations may increase the risk and severity of alopecia areata.

Acid can block TRPV3 from outside the cell but boost its function from inside.

The research found how GPCR Class A Rhodopsin receptors are related and suggested possible substances they interact with.

EPHA4 and Ephrin A3 are found in the skin of Aohan fine-wool sheep.

PRDX5 enzyme may contribute to alopecia areata by affecting oxidative stress and autoimmunity.

A mutation in the KRT82 gene is significantly associated with Alopecia Areata.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.