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Higher disease activity in systemic lupus erythematosus is strongly linked to more internal organ damage.

LSD1 is essential for healthy skin development and creating the skin's protective barrier.

Non-coding RNA boosts retinoic acid production and signaling, aiding regeneration.

GFRα2 is essential for controlling neuron size but not for target innervation in certain sensory neurons.

Higher MPV and CRP levels may indicate more severe alopecia areata.

The protein RSL4 is crucial for making root hairs longer by controlling genes related to cell growth.

RACB in barley is crucial for cell polarity and nucleus positioning, aiding fungal infection.

The fer-ts mutation in plants prevents root hair growth at high temperatures.

A new mutation in the STS gene causes X-linked ichthyosis, even in rare female cases.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

OsPHR2 gene causes excessive phosphate in rice shoots, affecting plant growth and root development.

A new enzyme, BSSP, is found in high amounts in the hair follicles of nude mice.

The Bsk mutation doesn't involve keratin gene recombination and its cause is unknown.

Arab APS1 patients have unique and recurrent AIRE gene mutations.

Hairless protein reduces Msx2 gene activity, affecting hair follicle development.

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

LHX2 is crucial for development, tissue repair, and preventing diseases.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

RHUPUS should be considered in children with deforming arthritis.

Scientists created cell lines to study a genetic skin disorder using CRISPR technology.

A rare genetic mutation causes resistance to vitamin D, leading to severe rickets and requiring high doses of calcium and vitamin D for treatment.

Higher RBP4 levels are linked to severe alopecia areata, but genetic variant rs3758539 doesn't affect baricitinib response.

Cox-2 significantly contributes to the development and progression of skin and esophageal cancers.

Erosive lichen sclerosus is a distinct subtype with specific skin features, and treatment led to complete resolution in half of the cases.

Reconstructed skin models are useful for studying how skin processes certain chemicals.

Far-infrared radiation improves stem cell growth and movement, helping heart therapy.

DS-2325a is safe and well-tolerated, supporting further development for Netherton Syndrome treatment.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

Four specific keratins in hair follicles help understand hair structure and function.

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