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Keratin 75 is important for fast wound healing and works with SOX2 and the LINC complex to help skin cells move and repair damage.

UVB exposure increases appetite by activating p53 in skin cells.

Nagashima-type palmoplantar keratosis in Asians is caused by a SERPINB7 gene mutation.

A rabbit gene important for hair development was identified and detailed.

The method effectively analyzes skin tissue changes, especially in the arrector pili muscle and nerve fibers with hair follicles.

PROTAC technology shows promise for cancer treatment but needs more effective E3 ligase recruiters.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

The technology can help diagnose and subtype autoimmune diseases by identifying specific autoantibodies.

PDF2 senses specific lipids and regulates root growth and gene expression in Arabidopsis.

The PIP5K1A gene helps cashmere growth in goats by promoting cell proliferation, and melatonin boosts its expression.

Panfolliculoma is a rare, non-cancerous growth related to hair follicles.

PSAT1 is key for hair growth and stem cell function in cashmere goats.

CHI3L1 and CXCL5 proteins help promote hair growth.

miR-199a-3p controls hair growth and is linked to alopecia areata.

A variant in the KRT31 gene causes a rare hereditary hair disorder called monilethrix.

MOF controls key genes for skin development by regulating mitochondrial and ciliary functions.

α- and γ-catenins help develop fetal skin by 23 weeks.

Mutations in Plcd1 and Plcd3 together cause severe hair loss in mice.

Plasmalogens activate a channel in cells that may stimulate hair growth.

Mutations in the PADI3 gene may cause central centrifugal cicatricial alopecia in women of African ancestry.

Tmem30b is essential for hearing by maintaining hair cell structure in the ear.

YAP and TAZ proteins are necessary for the development of two types of skin cancer.

The study concluded that PKP1 is essential for skin integrity and hair growth, and its dysfunction causes the symptoms of ectodermal dysplasia/skin fragility syndrome.

Type II keratins are uniquely phosphorylated during stress and mitosis, affecting their structure and function.

Sphingosine 1-phosphate affects inflammation and gene expression in different aorta cells.

α3β1-integrin is crucial for maintaining normal hair follicle shape and function but not needed for the development of the surrounding skin.