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Mice with extra human KLK14 had hair and skin problems, including weaker cell bonds and inflammation, linked to Netherton syndrome.

Different parts of the nail express different keratins, showing unique patterns of differentiation.

Keratin 18 helps diagnose and predict cancer progression and affects cancer growth and spread.

Cronkhite-Canada syndrome may be more treatable and less severe than previously thought.

Canine hair follicle cells show stem cell properties, aiding hair growth.

Nerve growth factor helps cashmere goat hair cells grow and is more active during the hair growth phase.

The TT genotype of a specific SNP in sheep is linked to better wool quality.

Syntaxin 9 helps in transporting and signaling of the EGF receptor in skin and stomach cells.

Damaging mutations in NFKB2 cause a severe and distinct form of primary immunodeficiency with early-onset and often ACTH-deficiency.

AL136131.3 slows hair growth by affecting energy processes in hair loss.

Netherton Syndrome is a non-treatable genetic disorder in children causing skin, hair, and allergy issues.

N-WASP is essential for normal hair growth in mice.

Cantú syndrome may be linked to pituitary adenomas.

Hair type differences in cashmere goats are linked to keratin and cytoskeletal organization.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

Ca²⁺-mediated protein citrullination controls cell growth in the CNS and may help treat brain tumors.

c-Myc, Max, and Bin1 help hair follicle cells mature and die.

The gene Prss53 affects hair shape and bone development in rabbits.

Key circRNAs play a role in wool follicle development, aiding in breeding better quality wool sheep.

Normal cells outcompete and remove mutant cells in the pancreas with the help of the EphA2 receptor.

Arg1+ macrophages may play a role in Alopecia Areata, offering new treatment targets.

Nociplastic pain is a complex, heritable trait with genetic links to chronic and neuropathic pain.

Different body areas have unique skin cell communication patterns, explaining why certain skin diseases occur in specific regions.

A new gene mutation causes complete androgen insensitivity in a 16-year-old with a female appearance.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

cDermo-1 causes dense skin, feathers, and scales in chickens.

Hair shaft changes may be linked to CCCA, but their role is unclear.

Alpha-difluoromethylornithine prevents cancer in mice but causes hair loss.