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The conclusion is that the nuclear lamina and LINC complex in skin cells respond to mechanical signals, affecting gene expression and cell differentiation, which is important for skin health and can impact skin diseases.

Hidradenitis Suppurativa is likely an autoinflammatory disease, and better understanding its causes could improve treatments.

The vitamin D receptor helps maintain hair and bone health even without binding vitamin D.

No effective treatment exists to stimulate hair growth in atrichia with papular lesions.

Modified HDL can better deliver drugs and genes, potentially improving treatments and reducing side effects.

Vitamin D receptor binds similarly to natural and synthetic ligands, affecting gene regulation.

Bald thigh syndrome in sighthounds is caused by structural defects in hair shafts due to downregulated genes and proteins.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

Human hair keratins K85 and K35 create unique filament patterns important for early hair formation.

Hard skin features like scales, feathers, and hair evolved through specific protein changes in different animal groups.

Human hair loss may have evolved to help increase brain size.

Increased FGFR2b signaling, influenced by androgens, plays a role in causing acne.

Two rare genetic diseases cause severe rickets in children due to defects in vitamin D metabolism.

The research showed that Vitamin D and its receptor are important for healthy bones and normal hair and skin in rats.

Two mouse mutants have defective hair cuticle cross-linking.

The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.

A girl with a rare skin condition called Keratosis Follicularis Spinulosa Decalvans showed no significant improvement with treatment.

The Wnt/β-catenin pathway is important for body functions and diseases, and targeting it may treat conditions like cancer, but with safety challenges.

Tiny RNA molecules help control the growth of plant hairs.

Putting thymidine dinucleotide on newborn mice's skin can delay and reduce skin cancer.

KFSD is a genetic disorder causing hair loss and skin issues, with no effective treatment.

Haplogroup X found in Altaian population supports Amerindian origin.

Blocking both main energy pathways can stop hair follicle stem cell-induced skin cancer growth.

Adjusting the medication tacrolimus resolved a boy's red nail beds after a stem cell transplant.

A patient with untreated congenital adrenal hyperplasia had large benign tumors in her adrenal glands removed, improving her symptoms.

Mice without Vitamin D receptors have hair growth problems because of issues in the hedgehog signaling pathway.

Foxi3 expression in developing teeth and hair is controlled by the ectodysplasin pathway.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

P-cadherin is important for hair growth and health, and its problems can cause hair and skin disorders.

The best animal model for studying male-pattern baldness is the stumptailed macaque, not rats or mice.