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Scientists found 53 keratin genes in yaks that are important for hair growth and share similarities with those in other animals.

Mutations in the KRT16 gene can cause skin and nail disorders.

SP1 promotes and KROX20 inhibits hair cell growth by affecting the CUX1 gene.

The E413K mutation in the hHb6 gene causes monilethrix, a hair disorder, but doesn't show consistent symptoms.

Keratin 75 might be important in oral cancer progression.

PRX102 is essential for rice root hair growth by helping transport substances to the tips.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

XEDAR triggers a specific signaling pathway in cells.

K6hf is found in specific parts of hair follicles, nails, and tongue, and is linked to hair growth and structure.

Krox20 is crucial for hair growth and maintaining skin stem cells.

QLT0267 stops hair follicle cell growth and movement.

Msx-2 gene removal speeds up skin wound healing in mice.

Ixekizumab is effective and safe for patients who did not improve with etanercept treatment for psoriasis.

A new protein, mK6irs, is found in specific hair layers and may help understand hair growth and diseases.

Krox20 is important for cell differentiation in the brain and hair follicles.

KGF-1 135 is a stable and effective alternative for treating oral mucositis.

BRL 7660, once studied for male contraception, showed promise as an acne treatment but was not developed further due to competing drugs.

KY19382 helps regrow hair and create new hair follicles.

Mosaic Klinefelter syndrome can affect male fertility and may be missed in routine tests.

Kawasaki's disease can occur in adults and should be considered with specific symptoms and high ferritin levels.

Bexxar is highly effective as a first treatment for non-Hodgkin's lymphoma, with most patients alive and many in remission after eight years.

Promising cancer treatments were found, but the manufacturer closed.

Msx2 is essential for proper enamel formation by preventing abnormal cell transformation.

Early and accurate diagnosis is crucial for managing rare genetic disorders like this localized variant of junctional epidermolysis bullosa.

The technology can create transgenic cashmere goats with improved wool quality.

A new EDA gene variant causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family.