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A specific gene region can control targeted and responsive gene expression in mice, useful for skin disorder treatments.

New RIPK4 gene mutations were found to cause a type of skin and limb birth defect.

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

High-intensity red LED light boosts bone cell growth and mineralization.

JAK inhibitors may help treat alopecia areata by reversing hair loss.

Dermal EZH2 controls skin cell development and hair growth in mice.

Skin organoids with NCSTN mutation show changes in hair follicle development and higher inflammation, key features of Hidradenitis Suppurativa.

The Hr protein binds to DNA, interacts with p53, and affects cell cycle genes.

Removing REDD1 in mice increases skin fat by making fat cells larger and more numerous.

Mutating the gmds gene in zebrafish increases hair cell numbers and regeneration.

HPV8 causes skin cancer by expanding specific skin stem cells.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

A specific DNA sequence caused hair loss in male mice by activating immune cells and increasing a certain immune signal.

A new compound was made that might help treat diseases related to male hormones.

CD80CD86 deficiency causes hair loss by disrupting regulatory T cells.

PSENEN gene mutations can cause both Dowling-Degos disease and acne inversa.

Dauricine may help treat certain brain cancers by reducing cancer cell growth and promoting cell death.

A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

Antizyme reduces tumor growth and normalizes skin cell development affected by MEK.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

Low IRES/Cap translation is linked to higher stem cell potential.