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Giving immune serum from vaccinated mice to mice without T cells prevents infection and tumor growth.

A new gene mutation is linked to monilethrix in the studied family.

Certain NK cell changes in blood may indicate alopecia areata progression.

Different types of cells in the eye express specific keratins at various stages of development.

Keratin-75 is secreted by ameloblasts in a unique way without a signal peptide.

Scientists discovered a unique hair protein, KAP24.1, with a special structure, found only in the upper part of hair cuticles.

Four new genes related to sheep wool were discovered, showing genetic diversity.

A specific gene mutation causes different hair defects in Indian monilethrix families.

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

Keratin gene clusters in humans and marsupials are similarly organized.

Too much IKZF1 and Ikaros protein may cause alopecia areata.

High DKK1 levels predict worse survival in head and neck cancer.

A stable, active version of a growth factor was made in bacteria, showing promise for medical use.

Trichohyalin helps in hair and skin cell structure and function by binding calcium and linking proteins.

Keratin 10 end domains may increase skin cancer risk by reducing cell death.

The hairless gene in Kunming mice is important for hair and skin, and shows genetic variations.

Tofacitinib helped a teenager with severe hair loss grow hair back, but more research is needed.

TYK2 inhibitors show promise for treating cancer and autoimmune disorders.

Certain genes influence immunoglobulin levels in Chinese Holstein cows, which can improve calf health.

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

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

PRC1 influences skin stem cell development by both turning genes on and off, affecting hair growth and skin cell types.

Sheep and goat hair fibers are complex due to keratin-associated proteins, which are important for fiber properties and growth.

A mutation in the hHb3 gene is linked to the hair disorder monilethrix.