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FOXN1 mutations can cause varying immune and physical issues, with severity influenced by gene activity and possibly other factors.

Using special RNA to target a mutant gene fixed hair problems in mice.

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

The peach gene pCTG134 helps control the interaction between auxin and ethylene hormones during fruit ripening.

High levels of ODC and a mutant Ha-ras gene cause tumors in mice.

R-spondin2 may help treat hair loss, gene differences could explain baldness, a peptide's regulation is linked to psoriasis, B-defensin gene copies may affect a skin condition's risk and severity, and potential markers and targets for alopecia areata were identified.

lncRNA MRPS28 regulates hair follicle development in cashmere goats, affecting cashmere quality.

The G allele of IFITM3 rs12252 is linked to more severe COVID-19.

The Thr1022Ala variant in the hairless gene is not a disease-causing mutation.

Researchers found that certain RNA circles in the brain are linked to disease risk, but their exact role in disease is still unknown.

Alopecia areata involves both innate and adaptive immunity, with specific genes linked to the disease.

Researchers created a model to understand heart aging, highlighting key genes and pathways, and suggesting miR-208a as a potential heart attack biomarker.

PRX102 is essential for rice root hair growth by helping transport substances to the tips.

A feedback loop between LRH and RSL4 controls root hair growth in Arabidopsis.

Two new gene mutations cause a rare hair disorder.

miR-5110 affects alpaca pigmentation by altering specific gene expressions.

Higher miR-34a levels and the A variant of the MIR-34A gene are linked to increased risk and severity of alopecia areata.

Nexin 1 may help control hair growth.

Deleting the CD271 gene in mouse skin cells leads to disorganized skin and increased hair growth, suggesting CD271 is important for skin health.

A genetic mutation caused severe rickets and alopecia in an Indian patient, but high-dose calcium and phosphate treatment improved their condition.

Neuronatin is found in various cells of rat tissues and has a unique location in sperm cells.

CT60 polymorphism might increase the risk of Alopecia Areata.

A new mutation in the human glucocorticoid receptor reduces its function and causes resistance to glucocorticoids.

Ribonucleotide excision repair is crucial to prevent skin cancer.

The KRTAP36-1 gene affects wool quality in Chinese Tan lambs.

Two new mutations in the AR gene linked to severe androgen insensitivity were found.

The ABCA4 gene protects hair follicle stem cells from toxic vitamin A byproducts.

A new goat gene affects cashmere fiber thickness; certain variations can make the fibers coarser.

Vitamin D receptor can control the hairless gene linked to hair loss even without vitamin D.