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Hox proteins help maintain keratinocyte identity by regulating miRNA expression.

New mutations in hair keratin genes cause the rare hair disorder monilethrix.

Interferon β from hair cells stops the growth of other hair cells.

The IRE gene is important for normal root hair growth in Arabidopsis plants.

Polyamines help fix DNA damage accurately in cells.

Arabidopsis Formin 2 stabilizes actin filaments, affecting cell-to-cell movement and virus susceptibility.

The LEF-1 binding site enhances gene expression in hair follicles, with other proteins aiding specific regulation.

A protein in plants needs to bind two lipids to help with root hair growth, and this process is similar across different plant species.

Frizzled 3 and Frizzled 6 together control the orientation of mouse hair follicles.

Removing a specific gene in certain skin cells causes hair loss in mice by disrupting hair follicle development.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

Trichohyalin in sheep hair follicles may help with structure and calcium binding.

Two new compounds can block androgen receptor activity in different ways and may lead to new treatments for androgen-related diseases.

Trichohyalin is a protein in hair follicles that helps form hair filaments.

Disulfide bonds are crucial for hair structure during keratinization.

Overexpression of hurpin in mice leads to abnormal skin and higher skin cancer risk.

The HIF-2α/ARNT complex is important for hair follicle development by controlling cell growth.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

TH antibodies in vitiligo and AA patients recognize the same protein parts.

Bikunin is found on the cell boundaries of certain skin layers and may help regulate skin and hair functions.

PIEZO1 helps keep hair follicle stem cells inactive, affecting hair growth.

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

The enzymes Tet2 and Tet3 are important for skin cell development and hair growth.

Researchers found a new gene, hacl-1, that is active in mouse hair follicles during hair growth and may be important for hair biology.

LHX2 is crucial for development, tissue repair, and preventing diseases.

A keratin hHb6 mutation causes a hair disorder with varying severity, influenced by other factors.

LHTric-1 is a specific antibody useful for studying hair and nail formation.

A point mutation in the androgen receptor gene causes complete androgen insensitivity.

The fuzzy gene is crucial for controlling hair growth cycles.