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Researchers found four key proteins that affect the development of a specific hair type in Yangtze River Delta white goats.

A patient with "strawberry gingivitis" improved after correct treatment for Granulomatosis with polyangiitis, highlighting the need for early diagnosis.

SLICK cattle have better heat tolerance due to specific gene expression and pathway differences.

Hedgehog signaling is essential for normal sebaceous gland development and affects keratin 6a expression.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

Progranulin overexpression leads to shorter, thinner hair and increased cell death in mouse hair follicles.

Biglycan helps regulate hair growth and regeneration.

Sea cucumbers have unique genes that help them regenerate their intestines.

The 190-kbp domain contains all human type I hair keratin genes, showing their organization and evolution.

GLABRA 2 controls ethylene production to help root hair growth during nutrient deficiency.

Inhibiting Bmp signaling disrupts hair growth and differentiation.

Keratin 17 gene mutations cause both steatocystoma multiplex and pachyonychia congenita type 2.

Trichothiodystrophy hair is structurally abnormal with protein and organization issues.

Two distinct pathways direct proteins to vacuoles in Arabidopsis, affecting root hair growth and protein targeting.

New gene variants were found for rare skin and hair disorders, improving understanding and treatment.

Overexpressing Dsg3 in mice skin causes excessive cell growth and abnormal skin development.

BMP2 helps hair follicle stem cells become specialized by increasing PTEN, which causes autophagy.

The wavy coat in NCT mice is caused by multiple genes, including a mutation in the Prss53 gene.

A chimeric keratin partially improved skin structure in mice lacking keratin 5, but didn't fully restore normal skin.

Certain skin proteins can form anchoring structures without the protein AMACO.

Different forms of FGF5 either promote or inhibit hair growth.

MARCKSL1 is important for wound healing and could be a target to reduce scarring.

Citrullinated proteins from Porphyromonas gingivalis may contribute to rheumatoid arthritis.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

Paeoniflorin protects brain cells by involving a specific protein and neurosteroids.

Tissue-engineered skin substitutes can model junctional epidermolysis bullosa and may help develop gene therapy.

The mutated hairless gene causes hair loss by acting as a new type of corepressor affecting thyroid hormone receptors.

New lipid/fiber microplexes improve mRNA therapy for degenerative diseases by enhancing cell function and treatment effectiveness.