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Removing myelin protein zero-like 3 in mice leads to better metabolism and resistance to obesity.

D-OCT shows increased blood vessel growth in response to tissue damage in Frontal Fibrosing Alopecia and is useful for diagnosis and monitoring.

FoxN1 overexpression in young mice harms immune cell and skin development.

TGF-β2 helps yak hair follicles enter the regression phase, while HSP70 tries to prevent it.

Keratinocyte gene expression is controlled by multiple modules with specific binding sites.

A specific type II hair keratin was identified and found in hair cortex and tongue cells.

The GH-IGF-I axis is likely involved in the hormonal imbalances seen in non-obese women with functional hyperandrogenism.

Zebrafish can help study and develop treatments for hearing loss.

Bimekizumab effectively treated a man's chronic beard hair loss.

The model improves understanding of androgen interactions by focusing on signal intensity and system capacity.

FERONIA and LRX proteins help control cell growth in plants by regulating vacuole expansion.

Different gene mutations cause different types of ichthyosis, with some new mutations found.

Reducing Flightless I protein improves wound healing by activating skin stem cells.

SWI/SNF complexes are crucial for wound healing but not for hair growth.

Mutations in the KRT85 gene cause hair and nail problems.

KRTAP2 genes are crucial for hair structure and may impact hair disorders and treatments.

MPZL3 protein is important for controlling hair growth cycles.

Folliculin slows hair growth, and blocking it might help treat hair loss.

IL-1 receptor absence in mice leads to skin cysts and changes in immune response after UVB exposure.

Different hair protein amounts change the strength of keratin/chitosan gels, useful for making predictable tissue engineering materials.

Hair proteins change location and structure as hair cells mature.

Hair cells grown in a lab showed specific hair proteins.

Activating PKCα in skin causes cell death and inflammation through different pathways.

The KRTAP7-1 gene is very similar across different cattle and yak breeds and likely plays a role in hair strength and shape.

The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.

Sfrp2 increases during hair follicle catagen phase and slows keratinocyte growth.

A new mouse gene, Keratin 17n, is mainly found in nail tissue and may explain why mice without Keratin 17 don't have nail issues.

Esrp1 is important for skin health by helping form and maintain the skin barrier.

Mutations in the KLHL24 gene cause a skin disorder in some Russian families.