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Thyroid hormones help hair grow, reduce hair loss, and increase hair pigment.

Epidermolytic ichthyosis can be inherited in a semidominant way with mild symptoms in carriers.

Three genes linked to the development of trichilemmal cysts were found.

Deleting the Hoxc13 gene in frogs shows its crucial role in developing skin structures similar to hair.

The harlequin ichthyosis mouse mutation causes thick skin and early death, resembling a human skin disorder.

Basal cell carcinomas may differentiate similarly to hair follicles and could be influenced by hair cycle-related treatments.

The study found that a key immune pathway protecting hair follicles is reduced in a mouse model of scarring hair loss.

Nestin identifies specific progenitor cells in hair follicles that can become outer root sheath cells.

Dermoscopic examination helps diagnose different types of hair loss conditions by showing specific patterns.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

New treatments targeting specific genes show promise for treating keratin disorders.

A second domain of high sulfur KAP genes on chromosome 21q23 is crucial for hair structure.

Mutations in the KRT85 gene cause hair and nail problems.

Methotrexate effectively treated a 2-year-old's generalized pustular psoriasis without side effects.

Two specific hair keratin genes are active during hair growth and decline as hair transitions to rest.

TCDD speeds up skin barrier formation by increasing certain gene expressions.

Scientists created a long-lasting stem cell line from human hair that can turn into different skin and hair cell types.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

KAP genes are crucial for hair development and show both shared and unique traits in humans, chimpanzees, and baboons.

Keratin genes change gradually during skin cell development and should be used carefully as biomarkers.

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

KAP genes show significant genetic variability, but its impact on hair traits is unclear.

The KRTAP11-1 gene promoter is crucial for specific expression in sheep wool cortex.

Some hair protein genes evolved early and were adapted for use in hair follicles.

The system allows precise control of gene expression in mouse skin, useful for studying skin biology.

Researchers mapped and categorized specific keratin-associated protein genes on human chromosome 21q22.1.

Hair keratin-associated proteins are essential for strong hair, with over 80 genes showing specific patterns and variations among people.

Human hair keratin genes are similar to mouse genes and are specifically expressed in hair follicles.

Scientists found 53 keratin genes in yaks that are important for hair growth and share similarities with those in other animals.