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A gene mutation in mice causes hair loss, weak bones, and protein buildup, showing how protein processing issues can lead to diseases.

Hair loss might be linked to eye aging due to inflammation markers in blood.

The MPV/PC ratio can help assess disease activity in alopecia areata.

Researchers found two new genetic variants linked to Alzheimer's disease.

Removing anthrax toxin receptor 1 in pigs prevents Senecavirus A infection and causes a rare disease similar to GAPO syndrome.

Alefacept showed some effectiveness for alopecia areata but needs more research.

A protein called ectodysplasin-A2 increases a hair growth inhibitor in balding cells, which could be a target for hair loss treatment.

A new method allows for controlled, long-lasting delivery of retinoic acid through the skin with fewer side effects.

Polydopamine is promising for personalized medicine and biomedical technology due to its strong adhesion and biocompatibility.

Machine learning can help find new ways to treat alopecia areata.

The HSD3B1 variant increases hair loss risk in overweight women with PCOS.

Upadacitinib may cause hair loss.

AHR ligands could treat inflammatory skin diseases.

Alopecia areata patients have higher IFN-γ and low vitamin D3 levels.

Certain gene variations are linked to alopecia areata.

HSP90 and lamin A/C are crucial for hair growth and could be targets for treating hair loss.

The scalp fat tissue of men with hair loss shows changes in gene activity that may contribute to their condition.

Dermoscopy is useful for diagnosing Atrichia with Papular Lesions in children without needing a biopsy.

The protein called small nuclear ribonucleoprotein polypeptide E is identified as a cause of a type of hair loss without other symptoms.

Men with a certain type of hair loss (AGA) have higher bad cholesterol and lower good cholesterol levels, making them more likely to get heart disease.

UVA-1 phototherapy might help treat alopecia areata.

Researchers created a new tool to measure the effects of alopecia areata from the patient's view, focusing on hair loss, daily life, and emotional health.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

Higher Alarin levels may predict androgenetic alopecia and metabolic syndrome.

Certain gene variations may increase the risk of hair loss in Egyptians.

Progerin affects cell shape but not hair or skin in mice.

A protein from fat-derived stem cells, DKK1, is linked to hair loss and blocking it may help treat alopecia areata.

Loss of Rap1 protein speeds up heart aging in mice.

IL-4 gene variation may increase the risk of alopecia areata in Turkish people.

People with androgenetic alopecia may have higher cholesterol and triglycerides, suggesting a higher risk of heart disease.