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Overexpressing SSAT in mice makes them highly sensitive to polyamine analogues, causing liver damage and high mortality.

Recessive X-linked ichthyosis involves a less efficient enzyme in hair follicles, suggesting two distinct enzymes.

Steroid sulfatase is important for activating hormones that affect memory, brain function, and certain diseases, and could be a target for treating hormone-related disorders.

New mutations in MBTPS2 reduce its function and cause IFAP syndrome with unusual symptoms.

EGFR hyperactivation increases sebaceous gland size and sebum production in mice.

Aging skin cells change their lipid profiles due to stress, affecting skin health.

Different sPLA2 enzymes affect immunity, skin and hair health, reproduction, and may be potential targets for therapy.

Overexpression of SSAT causes hair loss and skin issues, but reducing putrescine can help.

Oleoylethanolamide (OEA) safely boosts fat production in skin cells and may help treat dry skin and reduce inflammation.

A gene mutation in mice causes increased mast cells and disorganized hair follicles in their skin.

A sphingolipid from human placenta may help treat vitiligo by activating melanocyte stem cells.

Mice with too much sPLA₂-IIA have hair loss and poor wound healing due to abnormal hair growth and stem cell depletion.

sPLA2-IIA increases growth in hair follicle stem cells and cancer cells, suggesting it could be targeted for hair growth and cancer treatment.

Minoxidil sulfotransferase is a marker of keratinocyte differentiation and may play a role in hair growth.

Single Blimp1+ cells can create functional sebaceous gland organoids in the lab.

The Msi2 protein helps keep hair follicle stem cells inactive, controlling hair growth and regeneration.

A new method quickly creates controllable cell clusters for tissue engineering and drug testing.

Altering SSAT affects fat metabolism and body fat in mice.

A specific chemical change in the S100A3 protein leads to the formation of a four-part structure important for hair formation.

A new method efficiently creates cell spheres that help regenerate hair.

The SYP123-VAMP727 complex is important for transporting materials that harden the root hair shank in Arabidopsis.

Cholesterol sulfate buildup due to a genetic mutation disrupts the skin barrier, leading to the scaling skin seen in X-linked ichthyosis.

The Siah1 and Siah2 genes are active in mouse skin development and hair growth, especially right after birth.

Sebaceous lipids are crucial for keeping skin and eyes healthy in mice.

New mutations in the DSG4 gene cause a rare hair condition.

Enzyme purified and characterized for minoxidil sulphation in rat liver.

Hair growth-related cells need the enzyme SCD1 to help maintain the area that supports hair growth.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

MicroRNA-200 prevents sebaceous gland development by inhibiting SOX9 and cell cycle progression.