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Mutations at Val-889 and Arg-752 disrupt key interactions in the androgen receptor, affecting its function.

Junctional proteins stabilize the inner root sheath and connect the companion layer in human hair.

Keratin in mouse hair follicles is complex and plays specific roles.

A specific type II hair keratin was identified and found in hair cortex and tongue cells.

Meis2 is essential for touch sensation and nerve function in mice.

Dynamic, light touch is sensed through a common mechanism involving Piezo2 channels in sensory axons.

Maternal melatonin improves offspring hair growth by affecting specific proteins and pathways.

Some human genetic markers work for genetic studies in pig-tailed and stump-tailed macaques, which can help in their conservation.

Mutant Cx43 causes slower wound healing and hair growth issues in ODDD.

Pili torti hair twists due to uneven outer root sheath cell development.

Meis1 is crucial for skin health and tumor development.

MAIT cells may help fight COVID-19 but also contribute to severe inflammation.

Two mouse mutants have defective hair cuticle cross-linking.

A woman with a rare autoimmune disorder had a blister on her eye and unique immune reaction, which was effectively treated with medication.

The protein AtRXR3 limits root hair growth in Arabidopsis, affecting phosphorus uptake.

The harlequin ichthyosis mouse mutation causes thick skin and early death, resembling a human skin disorder.

Keratin 75 is important for fast wound healing and works with SOX2 and the LINC complex to help skin cells move and repair damage.

Trichothiodystrophy can be linked to urologic issues and high calcium in urine.

Presynaptic inhibition of certain nerve fibers in cats is mainly controlled by GABA and glycine.

The research found specific genes and pathways that control fur development and color in young American minks.

CTIP2 may help in skin development and maintenance.

A rat had a cyst similar to a hair follicle structure.

The mtDNA N haplogroup is linked to a higher risk of late-onset lupus and specific symptoms in Han Chinese women.

SkQ1 antioxidant improved health and lifespan in mice.

Reticular erythematous mucinosis syndrome can occur with minimal mucin deposition.

HT-scCAT-seq helps understand gene regulation in embryonic skin development.

Cat color patterns are determined early in development by gene expression and epidermal changes, with the Dickkopf 4 gene playing a crucial role.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.