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Scalp hair follicle cells help protect and heal skin in certain skin conditions.

A new gene mutation linked to KID syndrome was found, expanding genetic knowledge.

The gene therapy showed significant wound healing and was safe for treating severe RDEB.

Goats' hair and color traits are linked to specific RNA expressions, useful for breeding and textiles.

Certain mutations in the PADI3 gene may increase the risk of developing a type of scarring hair loss common in women of African descent.

HLA-DRB5 and other genes may be linked to alopecia universalis.

A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

The mutation causes hairless mice due to mislocalized and dysfunctional HR protein.

A cat's poor wound healing was linked to a genetic deletion in the COL5A1 gene.

PAD enzymes play a key role in hair growth and structure.

Super-enhancers control CD25 expression in specific cell types, affecting immune function.

Increasing neurotrophin 4 in skin boosts nerve endings but not sensory neuron count.

CLEC4D gene variants may increase the risk of alopecia areata in Jordanians.

A mutation in the vitamin D receptor causes severe resistance to vitamin D, affecting bone health but not hair growth.

Poly(ADP-ribose) synthesis is linked to skin cell differentiation.

Frizzled 3 and Frizzled 6 together control the orientation of mouse hair follicles.

Certain genes may help Bulgarians live longer.

A mutation in the iRhom2 gene causes hairless mice due to abnormal hair follicle development.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

An individual's morning or evening preference can predict changes in their body clock gene expression.

A new syndrome, Teelwani Syndrome, combines features of two rare genetic disorders.

Mutant Cx43 causes slower wound healing and hair growth issues in ODDD.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

The prolactin gene polymorphism doesn't affect cashmere quality in these goats.

BTNL proteins help control inflammatory bowel disease by maintaining specific immune cells.

Basonuclin may help control ribosomal RNA gene activity in skin cells.

The study mapped keratin 15 and 19 genes, aiding future genetic disorder research.

Certain mutations in the hairless protein disrupt its ability to regulate the hair cycle.

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

Mouse Scube3 affects teeth, tongue, vibrissae, and eye development, but not facial structure or limb growth.