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Increased HIF-1α is linked to the inflammation and severity of hidradenitis suppurativa, suggesting treatments that lower HIF-1α could help.

K6hf is a unique protein found only in a specific layer of hair follicles.

A truncated protein linked to breast cancer may change cell adhesion.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

hsa_circ_0002980 can help stop liver cancer cells from growing and spreading.

Human hair follicles produce and respond to erythropoietin, helping protect against stress.

The SHJH hr mice with a mutated Hr gene show signs of faster skin aging due to poor antioxidative protection.

The Hr protein binds to DNA, interacts with p53, and affects cell cycle genes.

Certain genetic factors may contribute to frontal fibrosing alopecia in Brazil.

H. pylori infection may be linked to the hair shedding condition Telogen Effluvium.

Erythropoietin overexpression disrupts hair growth and fat formation in mice.

Targeting impaired Nrf2 signaling might help treat hidradenitis suppurativa early on.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.

A mutation in the hairless gene speeds up severe itchy skin in mice on a special diet.

A new genetic mutation in mice causes permanent hair loss and skin wrinkling.

The Hairless gene is crucial for healthy skin and hair growth.

HR protein causes abnormal hair cycles by increasing Tgf-β2 and reducing miR-31.

Overexpression of HDGF in melanocytes does not cause cancer.

Human placenta extract reduces inflammation and symptoms in atopic dermatitis.

The HGCA tool helps identify genes that work together by analyzing their co-expression patterns.

Mice with human-like EGFR had growth issues, skin defects, heart problems, and unusual bone development.

Mutations in the hairless protein gene cause hair loss.

Removing a specific gene in certain skin cells causes hair loss in mice by disrupting hair follicle development.

A mutation in the hHb3 gene is linked to the hair disorder monilethrix.

Researchers found a new mutation causing total hair loss from birth.

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

A faulty KLHL24 gene leads to hair loss by damaging hair follicle stem cells.

HGF activator helps convert HGF to its active form, promoting hair growth.