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The wavy coat in NCT mice is caused by multiple genes, including a mutation in the Prss53 gene.

Alkaline phosphatase activity decreases in early alopecia areata.

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

Hoxc13 regulates specific hair protein genes on mouse chromosome 16.

A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.

Staphylococcus aureus delays wound healing by disrupting lipid metabolism in skin cells.

YAP and TAZ proteins are necessary for the development of two types of skin cancer.

The AAPPO questionnaire is a reliable tool for assessing hair loss impact in alopecia areata patients.

Mutations in the SNRPE gene cause hereditary hair loss.

Egfl6 is not needed for zebrafish face development.

Quercetin significantly helps hair growth by activating hair follicles and improving blood vessel formation around them.

KRTAP2 genes are crucial for hair structure and may impact hair disorders and treatments.

p2y5, now called LPA6, is a receptor important for human hair growth.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

3,4,5-tri-O-caffeoylquinic acid promotes hair growth by activating the β-catenin pathway.

The CD44-CD49d complex boosts T cell activation and survival in autoimmune disease.

The frizzy mouse and hairless rat mutations are due to changes in the Prss8 gene.

4-aminopyridine speeds up and improves skin wound healing.

The baby’s hair loss was due to a rare genetic condition, not treatable by usual methods.

Alopecia areata is an autoimmune condition causing hair loss due to the immune system attacking hair follicles, often influenced by genetics and stress.

Defective nuclear transport may cause gene expression changes in Progeria.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

Certain genetic variants in ERN1, TACR3, and SPPL2C are linked to when Alzheimer's disease starts.

A new mouse mutation causes skin and hair defects due to a gene change.

Botulinum toxin type A helps treat hair loss by stopping cell death in hair follicles through a process involving certain non-coding RNAs and a protein called Bax.

Certain proteins are essential for the growth of root hairs in barley.

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

RNA-based treatments show promise for managing Hutchinson-Gilford Progeria Syndrome.

LPR1 regulates root growth under low phosphate stress independently of SIZ1 in Arabidopsis thaliana.