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The research cloned keratin 7 genes from humans, mice, and marsupials, found similarities between human and mouse genes, and discovered new areas of K7 expression in mice.

Cathepsin L deficiency causes hair and skin issues in mice.

The dog's health improved after treatment with antibiotics and other medications.

The CUBIC protocol allows detailed 3D visualization of proteins in mouse skin biopsies.

Krt15+ cells in mice can resist radiation, regenerate tissue, and start tumors, suggesting new cancer treatment targets.

BLTP1 and KIF27 gene mutations can help breed better wool sheep.

Ketoconazole loaded solid lipid nanoparticles can penetrate skin better than regular drug suspension and marketed product, providing slow, sustained release and improved stability.

The KEBOT system is a highly accurate AI tool for analyzing hair transplants.

The kitten's skin condition improved significantly after 4 weeks of treatment.

Integrin-linked kinase is crucial for normal skin healing.

KRT2.13 gene is similar to KRT2.9 but not expressed in hair follicles.

iNKT cells help develop and maintain healthy skin in young mice.

ATR12-351 ointment safely delivers LEKTI protein to the skin, reducing enzyme activity in Netherton syndrome.

Akt2 protein is essential for normal cell division in early mouse embryos.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

ILK is essential for proper hair follicle development and structure.

Human tissue kallikreins help regulate skin barrier functions and affect skin health.

Kūlaris improved quality of life for acne sufferers without side effects.

ILK is essential for skin development, pigmentation, and healing.

Keratin K6irs is a marker for the inner root sheath of hair follicles in mice and humans.

CLK1 is needed for skin cells to become epidermal cells but not sebocytes.

The K14 promoter is more active in skin cells than the K5 promoter.

Keratin 19 forms less stable and shorter filaments than keratin 14, giving unique traits to certain skin cells.

K31 can identify clear secretory cells in human sweat glands.

Krt6a-Cre transgenic mice help study gene effects on hair follicle development and tumor suppression.

Mice with extra human KLK14 had hair and skin problems, including weaker cell bonds and inflammation, linked to Netherton syndrome.

Pallister-Killian Syndrome is a complex genetic disorder requiring coordinated care and genetic counseling.

DS-2325a is safe and well-tolerated, supporting further development for Netherton Syndrome treatment.