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The new hydrogel helps heal diabetic wounds by reducing inflammation and improving tissue repair.

Injecting hyaluronidase into the artery is effective for treating skin death and hair loss caused by hyaluronic acid fillers.

Using both hyaluronic acid compounds together improves skin hydration and reduces wrinkles better than using one alone.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Disrupting the Hars2 gene in mice causes hearing loss due to mitochondrial problems and hair cell damage.

Truncated hHb1 keratin may play a role in breast cancer cell transformation.

A common mutation in the hHb6 gene is linked to monilethrix, but other factors may also play a role.

hHbl gene is active in hair shaft cells and some pilomatricomas.

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.

SAHA syndrome is a condition in women involving skin and hair issues, often related to hormonal imbalances, and is treated based on the underlying cause.

DA-MeHA hydrogel effectively aids stem cell-based skin regeneration.

Using human recombinant hyaluronidase in donor strip harvesting may improve the procedure.

HtrA2 activity is crucial for normal hair growth by regulating fat cell development.

HAPLN1 can promote hair growth and may help treat hair loss.

Combining hyaluronic acid and oxygen may help improve urinary incontinence in menopausal women.

Low temperatures don't harm hyaluronic acid's healing abilities.

The 5050 MHA42MCS45 hydrogel blend is suitable for repairing load-bearing soft tissues.

Calcium hydroxylapatite can be successfully integrated into healing skin and stimulates collagen.

A unique gene mutation was found in a family with monilethrix.

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HYDRO DELUXE BIO hyaluronic acid hydrogel is compatible with skin cells, may reduce inflammation, promote blood vessel growth, and protect against oxidative stress, suggesting it could help revitalize hair follicles.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

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

Certain HLA class II alleles increase or decrease the risk of alopecia areata.

The hr gene is linked to hair loss in Valle del Belice sheep.

Whn is crucial for hair growth in certain areas by controlling a specific gene.

SAHA syndrome links oily skin, acne, excess hair, and hair loss in women, similar to PCOS.

The hexosamine pathway helps protect skin cells from stress and may improve skin and hair health.

The hr gene is crucial for skin and hair health, with mutations causing hair disorders.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.