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A new pair of mouse keratins, 65 kD and 48 kD, are found in specific skin areas and are linked to a unique skin differentiation type.

Astrotactin-2 is cleaved in a specific way that helps understand its maturation.

Pygopus 2 helps ovarian cancer cells grow by aiding ribosomal RNA production, independent of Wnt signaling.

High TSPEAR levels in colorectal cancer predict worse outcomes.

Ethosomes are effective, safe carriers for delivering drugs through the skin.

The transporter protein SH1446 in Staphylococcus hominis is key to underarm odor production.

The KRTAP21-1 gene affects wool yield and can help improve wool production.

The Eda gene helps regulate the hair cycle in goats.

Mice with human-like EGFR had growth issues, skin defects, heart problems, and unusual bone development.

Kaposi's sarcoma lesions might originate from benign tissue changes.

PAD3 plays a key role in hair and skin protein structure and may be linked to skin diseases.

A specific type II hair keratin was identified and found in hair cortex and tongue cells.

A rare gene mutation causes skin fragility and itching without affecting hair or nails.

Translation levels actively determine keratinocyte cell fate.

Protein microarrays are highly sensitive tools useful for disease diagnosis and studying proteins.

5α-reductases increase epitestosterone's effect on androgen receptors.

Epiprofin helps cells grow in developing teeth, hair, and limbs.

LHX2, with other markers, can identify hair placodes in rats.

61 functional keratin genes were identified in dogs and horses, leading to updated gene annotations.

Low fucosylation boosts stem cell growth in the eye.

Certain gene changes in osteopontin are linked to higher risk of atopic dermatitis and asthma.

Bikunin is found on the cell boundaries of certain skin layers and may help regulate skin and hair functions.

Overexpression of PKCepsilon leads to increased TNFalpha, promoting metastatic squamous cell carcinoma in mice.

Trichohyalin, a hair follicle protein, has a part with repeating patterns of 23 amino acids.

ANE syndrome is caused by a mutation in the RBM28 protein that disrupts ribosome assembly.