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

FERONIA and LRX proteins help control cell growth in plants by regulating vacuole expansion.

Vimentin and keratin help viruses spread and could be targets for antiviral treatments.

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.

A boy with a rare birthmark called verrucous hemangioma needed careful timing for surgery due to its size and depth.

Very-long-chain acyl-CoA synthetases and fatty acid transport proteins play key roles in fatty acid metabolism and lipid processing in different tissues.

The DWLSM provides detailed imaging of hair shafts and follicles with high accuracy.

HVDRR is caused by VDR gene mutations, leading to vitamin D resistance, treatable with high calcium doses, but alopecia remains permanent.

Nocturnal calcium infusions improved a boy's severe rickets without causing hair loss.

Valproic acid can cause a skin condition called leukocytoclastic vasculitis, which usually gets better after stopping the drug.

RCVS should be considered in thunderclap headaches, and MRA and DSA are better for diagnosis than CT angiogram.

Proper niche formation in Drosophila requires Slit-Robo signaling for cell migration.

Phospholipase C-δ1 is crucial for normal hair development.

Vitamin C derivative reduces hair loss-related protein in cells.

Krt16-deficient mice help understand skin disorders like PC and FNEPPK.

BK and Kv4.2 channels help Merkel cells in rat whiskers sense touch.

Turkish Van cats' genotypes don't affect traits like eye color or hair length.

New RIPK4 gene mutations were found to cause a type of skin and limb birth defect.

COVID-19 infection or vaccination may trigger lichen planus.

Cathepsin L is essential for normal hair growth and development.

Mouse models help target specific genes in lymphatic cells for research.

Suppressing very long chain fatty acids is linked to skin cancer.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

Lymphatic vessels develop from various cell types and mechanisms, not just veins.

The protein FLCN is involved in cellular cleanup and is regulated by ULK1.

CXXC5 is a protein that prevents hair growth and could be a target for hair loss treatment.

A vitamin D receptor mutation causes rickets and affects immune responses.

LLPS is crucial for RALF signaling, aiding plant growth and stress resilience.

Early treatment with corticosteroids improved her eye condition significantly.