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Melamax® protects skin from UV damage and reduces inflammation and oxidative stress.

MSC-Exos can aid organ development and offer therapeutic benefits for various conditions.

Sox9 is present in most canine skin tumors and may help understand stem cells' role in these cancers.

Microneedles offer a promising, less invasive way to treat and monitor psoriasis.

Scientists made a mouse model of a serious skin cancer by changing skin cells with a virus and a specific gene, which is similar to the disease in humans.

SCD1 inhibitors can cause skin issues in rodents.

The method effectively showed that the two exemestane preparations are bioequivalent.

HT-scCAT-seq helps understand gene regulation in embryonic skin development.

A(1-7) treatment reduces symptoms of lupus in mice.

FM dyes effectively stain Merkel cells for long-term observation.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

MTS effectively improves hair density and thickness in menopausal women with hair loss.

Tabby mutations in mice affect hair follicle development and help study genetic mapping and certain medical conditions.

Astaxanthin is a safe antioxidant that may improve heart, skin, eye health, and physical performance, and help manage chronic diseases.

LSD1 is crucial for regenerating hair cells in zebrafish.

A 15-year-old girl has a skin condition causing blisters on her feet, likely inherited from her family.

Matrix changes and increased MMPs contribute to skin inflammation in hidradenitis suppurativa.

S-Methylmethionine sulfonium can protect skin from UVB damage.

Identical twins with a rare KRT 86 gene mutation both have the hair disorder monilethrix.

The 3D-SeboSkin model effectively simulates Hidradenitis suppurativa and is useful for future research.

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

Blocking the enzyme 11β-HSD1 might help treat obesity and metabolic issues.

PH-762 shows promise in treating skin cancer by effectively targeting and silencing PD-1 in tumors with minimal side effects.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

A mutation in the SREBF1 gene causes both hereditary mucoepithelial dysplasia and IFAP syndrome, which are related conditions.

Human skin cells contain Protease Nexin-1, and male hormones can decrease its levels, potentially affecting hair growth.

A chromosomal change may cause ectodermal dysplasia and developmental issues in a child.

A 6-year-old girl was diagnosed with a rare hair disorder and started treatment with topical minoxidil.