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A specific hair protein variant increases the spread of breast cancer and is linked to worse survival rates.

TSC2-/meth cells can cause skin lesions, hair growth, and lung issues, and may be treated with chromatin remodeling agents.

p63 is essential for activating and differentiating stem cells in the nose's olfactory tissue.

Heat shock protein 27 is more present in the active growth phase of human scalp hair follicles.

Hirosaki hairless rats have sparse, twisted hair due to missing hair keratin genes.

Scientists created a detailed map of gene activity in different parts of human hair follicles.

The type 3 IP3 receptor is important for controlling hair loss and growth.

Gene expression regulates keratin production for normal hair growth.

Hox proteins help maintain keratinocyte identity by regulating miRNA expression.

A high-fat diet may weaken tongue structure by reducing certain protein genes.

DNA methylation changes are linked to hair growth cycles in goats.

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

Keratin 15 is not a reliable sole marker for identifying epidermal stem cells because it's found in various cell types.

Runx3 helps determine hair shape.

TCDD changes skin cell growth and keratin production in mice.

The gene Foxq1, controlled by Hoxc13, is crucial for hair follicle differentiation.

The RNA AL136131.3 slows down hair growth and speeds up hair loss by affecting sugar breakdown in hair follicles.

Deleting the MAD2L1 gene in mice led to rapid tumor growth despite chromosomal instability.

Stem cell behavior varies with stimuli, and lineage changes can happen without affecting stem cell division.

Sox13 is a new marker for early hair follicle development and differentiation.

The HoxC gene cluster and its enhancers are essential for developing hair and nails in mammals.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

Mutations in the Sgk3 gene cause fuzzy hair in mice.

Keratin structure in hair is stable at pH 5-6 but disrupts between pH 6-7.

A specific gene mutation in Japanese people can cause varying degrees of hair thinning in adulthood.

The conclusion is that the IL-6/STAT3 activation affects p63 expression in healing wounds, which may help in hair follicle regeneration.

Researchers identified potential markers for human hair color stem cells.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.