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The androgen receptor gene doesn't affect women with recurrent spontaneous abortions, but having a mutant genotype might protect against it.

A specific gene change is linked to severe hair loss.

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

A mutation in the human hairless gene causes alopecia universalis.

XEDAR triggers a specific signaling pathway in cells.

Nelfb is essential for dermal fat development and survival.

Reducing SFRP1 can promote hair growth and may help treat hair loss.

PCAT1 helps hair growth by controlling miR-329/Wnt10b.

FoxN1 overexpression in young mice harms immune cell and skin development.

Researchers found an RNA transcript that might help control a growth factor linked to tumor development.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

RUM-loaded SLN shows promise for treating acne and hair loss topically.

NDRG1 protein helps infantile hemangioma, a common infant tumor, to grow, and its mismanagement by FOXO1 protein plays a big role in causing the tumor.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

A specific RNA increases hair stem cell growth and skin healing by affecting a protein through interaction with a microRNA.

lncRNAs are important for understanding and treating skin diseases.

The ACE1 gene variant doesn't affect long-COVID symptoms.

Type I keratin genes are closely linked to the rex locus on mouse chromosome 11, affecting hair development.

IL-1 receptor absence in mice leads to skin cysts and changes in immune response after UVB exposure.

POUF51 and HES3 are key in controlling stem cell numbers in psoriasis.

Nails are essential for fingertip regeneration.

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

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

There is no significant link between the MMP-1 rs1799750 polymorphism and androgenetic alopecia in the Indonesian population.

Loss of Rap1 protein speeds up heart aging in mice.

The mutated hairless gene causes hair loss by acting as a new type of corepressor affecting thyroid hormone receptors.

Loss of OGG1 increases skin inflammation and auto-antibodies in lupus.

The FRZB gene slows hair growth in rabbits.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

The gene for Marie Unna hereditary hypotrichosis is located on chromosome 8p21, near the hairless gene.