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A specific RNA molecule, circCOL1A1, affects the growth and quality of goat hair by interacting with miR-149-5p and influencing cell growth pathways.

A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

PSAT1 is key for hair growth and stem cell function in cashmere goats.

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

RNase L suppresses regeneration in mammals.

Two new gene clusters important for hair formation were found on human chromosome 11.

A new genetic tool improves the study of hair growth and potential hair disorder treatments.

Pachyonychia congenita is linked to a keratin gene on chromosome 17.

Researchers found a gene mutation responsible for a rare hair loss condition.

All-trans retinoic acid helps amelanotic melanocytes in hair follicles develop and produce pigment while reducing their growth.

The hairy ear mutation in mice is linked to changes in gene expression affecting hair growth.

Regulatory T cells help prevent autoimmunity and have potential for treating autoimmune diseases.

Altering the keratin 17 gene in mice hair follicles caused temporary hair issues, but changes were minimal and short-lived.

New genetic mutations causing hair loss were found in a Chinese family.

Retinoids can help treat skin pigmentation disorders by affecting melanin production.

A young patient with unusual insulin resistance and high testosterone levels had a rare INSR gene mutation.

Tofacitinib is a promising treatment for children with rheumatic diseases.

Blocking a certain signal in the gp130 receptor can improve tissue healing and lessen osteoarthritis symptoms.

RCS-01 cell therapy is safe and improves skin gene expression.

A specific gene mutation causes vitamin D-resistant rickets and hair loss.

A specific gene segment can make mouse skin cells glow, helping study hair growth and gene effects.

A new gene mutation causes female pseudohermaphroditism due to glucocorticoid resistance.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

Rac1 is essential for proper hair structure and color.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.

The TRPV3 gene mutation affects hair growth by keeping mice in the growth phase longer, which could help treat hair loss.

Ritlecitinib effectively treats alopecia areata in patients 12 and older with fewer side effects.

TGM3 is important for skin and hair structure and may help diagnose cancer.

Twist1 is crucial for UVB-induced skin cancer development.

A specific gene mutation causes Olmsted syndrome.