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Staphylococcus aureus affects immune responses and skin cells in atopic dermatitis, suggesting new treatment targets.

ABCD1 gene mutations cause adrenomyeloneuropathy, leading to symptoms like limb weakness and spasticity, with management focusing on rehabilitation and spasticity treatment.

CRISPR/Cas systems show promise for cancer treatment by targeting miRNAs, but delivery and specificity challenges remain.

ELIP-based CRISPR delivery improves heart disease gene editing but needs more testing.

New partnerships, clinical trials, and drug approvals marked progress in therapeutic delivery in July 2018.

Stem cell therapy shows promise for better diabetic wound healing.

New therapies for Birt–Hogg–Dubé syndrome are being developed based on understanding the FLCN gene's role.

Men with hair loss have more DNA changes in back-of-head hair follicles, possibly protecting them from thinning.

The gene NM_026333 slows down aging by affecting the NCX1 pathway and could be targeted for anti-aging treatments.

Researchers identified five new potential targets for leishmaniasis treatment, suggesting repurposing existing drugs could be effective.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

Exosomes could be effective for improving skin health and treating skin diseases.

PEVIII is a promising treatment for Pseudomonas aeruginosa keratitis.

Collagen scaffolds in cell therapy can transform skin to be more resilient and pressure-responsive.

Cells that move well may improve hair loss treatments by entering hair follicles.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

The protein STAT3 slows down cell growth by blocking the FST gene, which affects hair development in sheep.

A mutation in the hairless gene speeds up severe itchy skin in mice on a special diet.

Staphylococcus aureus delays wound healing by disrupting lipid metabolism in skin cells.

A genetic defect in an Appenzeller Mountain Dog caused skin issues, improved with ketoconazole, showing the importance of advanced genetic testing.

WNT10A gene mutations cause short anagen hair syndrome.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

A new technology showed that the SOX9 gene might control heart scar formation after injury, suggesting new treatment possibilities.

CRISPR/Cas9 and prime editing can potentially fix skin disorder genes safely and effectively.

Lower PPARγ levels and specific gene variations are linked to more severe Frontal Fibrosing Alopecia.

IGN genes may regulate hair growth and could be targeted for hair-loss treatments.

CNGA3, GLUD1, and SIRT1 are promising targets for treating aging and glioblastoma.

Effective PCOS treatments require targeting specific signaling pathways.

Peptide nanoparticles can effectively deliver CRISPR-Cas9 to target KRAS mutations in cancer.

The composition with carnitine, thioctic acid, and saw palmetto extract may effectively reduce inflammation in hair follicle cells.