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CaBP1 and CaBP2 are important for continuous hearing by preventing inactivation of calcium currents in ear cells, with CaBP2 also able to restore hearing when reintroduced.

The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.

Targeting DKK3–CKAP4 can help reverse hair loss in androgenetic alopecia.

MsPG3 protein gathers at root hair tips, aiding growth.

PRC1 is essential for proper skin development and stem cell formation by controlling gene activity.

Truncated LTBP-1 disrupts TGF-β signaling, affecting hair growth.

TCDD reduces EGF receptors in the liver, affecting growth and development.

3D spheroid cells effectively test hair growth compounds like Minoxidil.

Common variants in the Trichohyalin gene are linked to straight hair in Europeans.

Type III collagen increases in recovering guinea pig skin, aiding tissue stability.

Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.

The LAMTOR3 gene is involved in cashmere goat hair growth and is affected by certain treatments and other genes.

NuMA-microtubule interactions are crucial for proper skin structure and hair growth.

The study found that p63 needs signals from morphogens to help skin cells differentiate properly.

PAD type III enzyme is specific to rat skin and hair follicles.

NAC1 controls certain enzymes that reduce root hair growth in Arabidopsis.

FGF13 gene changes cause excessive hair growth in a rare condition.

The study revealed the detailed structure of a keratin dimer, aiding understanding of how intermediate filament proteins function.

A gene mutation in Lama3 is linked to a common type of hair loss.

DAB labeling effectively identifies collagen type III and PDGFR in horse skin, but may show false positives.

Basonuclin 2 is vital for the development of facial bones, hair follicles, and male germ cells in adult mice, and its absence can lead to dwarfism and abnormal follicles.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

The B2 genes are crucial for hair growth in rats.

Mutations in Plcd1 and Plcd3 together cause severe hair loss in mice.

Scientists successfully purified a protein called Wnt3a, which is involved in processes like hair growth, but the overall yield was low, suggesting more work is needed to improve this.

The TRPV3 ion channel is important for skin and hair health and could be a target for treating skin conditions.

Twist1 helps maintain important features of cells crucial for hair growth by working with Tcf4 and β-catenin.

Men with balding at age 45 had higher IGF-1 and lower IGFBP-3, suggesting these factors might be important in male pattern baldness.

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

CaBP1 and 2 are necessary for maintaining calcium currents and hearing in inner ear cells.