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The human scalp hair bulb contains different types of melanocytes with varying abilities to produce melanin.

Protein kinase C epsilon may increase skin cancer risk by affecting nearby cells.

Poncirin is a promising inhibitor of Janus Kinase 3, potentially better than tofacitinib.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

Disruptions in epidermal polarity genes can lead to skin diseases.

A mutation in the vitamin D receptor causes severe resistance to vitamin D, affecting bone health but not hair growth.

A new genetic variant causes BRESHECK syndrome by disrupting cell growth and stress response.

Mutations at Val-889 and Arg-752 disrupt key interactions in the androgen receptor, affecting its function.

Hard α-keratins stay stiff in water because the surrounding matrix keeps them dehydrated and strong.

Hair follicle stem cells can become corneal-like cells with the help of pax6.

RXRα is crucial for hair growth and skin cell function.

Clim proteins are essential for maintaining healthy corneas and hair follicles.

The study concludes that certain domains in Clostridium histolyticum enzymes are structurally unique, bind calcium to become more stable, and play distinct roles in breaking down collagen, with potential applications in medicine and drug delivery.

Different PADI isoforms help cells develop diverse functions.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

RD26 controls root hair growth during drought by repressing key genes, helping plants save energy.

Increasing PBX1 reduces aging and cell death in hair follicle stem cells by boosting SIRT1 and lowering PARP1 activity.

Keratin 79 marks a new group of cells that are key for creating and repairing the hair follicle's structure.

Serotonin helps wounds heal faster.

FOL-026 peptide can help repair blood vessels and promote growth, offering potential treatment for vascular diseases.

RXRa is crucial for Th2 immune cell development and may link nutrition to immune health.

A 15-year-old with KID syndrome developed a rare skin condition called PEHFN.

Key genes can rewire networks, changing skin appendage types.

Vitamin D receptor can control the hairless gene linked to hair loss even without vitamin D.

Keratins are crucial for hair strength, and mutations in certain keratin genes cause hair disorders.

Lack of cystatin M/E causes thin hair and dry skin.

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

A new mutation in mice causes crooked whiskers and messy hair.