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Zfp157 is active in many mouse tissues during development and in specific adult cells.

hHb1, hHb3, and hHb6 mRNAs start expressing at the same time in hair follicles.

Ptprq has multiple forms that change during inner ear development.

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

A gene called Gk5 controls lipid production in the skin and affects hair growth.

CRABP2 helps increase the growth of cells important for hair growth by activating a specific growth pathway.

Claudin 6 is crucial for normal skin and hair development.

Pitx2 helps outer root sheath cells differentiate but can't start hair growth on its own.

A new goat gene affects cashmere fiber thickness; certain variations can make the fibers coarser.

Kartogenin may help treat hair loss by promoting hair growth and extending the hair growth phase.

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

GTL1 is needed to control root hair growth and prevent problems when there are too many nutrients.

CTCF protein is essential for skin and hair follicle development in mice.

ACKR2 helps prevent skin scarring and hair loss by controlling inflammation.

The research showed that CRISPR/Cas9 can fix mutations causing a skin disease in stem cells, which then improved skin grafts in mice, but more work on safety and efficiency is needed.

Keratin 17 gene mutations cause both steatocystoma multiplex and pachyonychia congenita type 2.

Prolactin affects the production of different keratins in human hair, which could lead to new treatments for skin and hair disorders.

Trichosanthes kirilowii extract helps wounds heal faster.

Recombinant keratin materials may better promote skin cell differentiation than natural keratin.

Keratin K80 is an ancient protein found in various tissues, important for cell structure and tissue differentiation.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

DPR can show different hair characteristics, as seen in two brothers with normal hair.

The HCR gene contributes to psoriasis risk.

Modified KGF mRNA helps skin cells grow and move faster, which may improve wound healing.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

K16 can partially replace K14 but causes hair loss and skin issues.

Ptch2 plays a key role in controlling stem cell function and the ability to regenerate after birth.

EGFR helps mouse hair follicles stop growing by reducing certain growth regulators.