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

The Foxn1(-/-) phenotype disrupts hair growth and affects skin stem cells.

D-004 shows moderate antidepressant effects but is less effective than Sertraline and Imipramine.

Reducing immunosuppression and using antiviral creams improved the woman's skin condition.

Familial dyskeratotic comedones are a rare, benign skin disorder that is hard to treat.

Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.

Farudodstat may help treat alopecia areata by protecting hair follicles.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

The new ddPCR method reliably detects unwanted viruses in CAR-T cell products, ensuring their safety for patients.

Small molecule treatments improve the ability of human amniotic fluid stem cells to become different cell types.

Spheroid culture in agarose dishes improves survival and nerve cell growth in thawed human fat-derived stem cells.

Frontal Fibrosing Alopecia might be an autoimmune disease.

The flutamide-loaded hydrogel is a promising, skin-friendly treatment for acne and hair loss, potentially requiring less frequent application.

SB414 may be an effective treatment for atopic dermatitis by reducing swelling and bacterial infection.

Amino acid storage proteins are essential for maintaining stem cells in female fruit flies.

Increased HSD11B1 enzyme expression is linked to higher body fat and insulin resistance.

M1 homeopathic complex may help slow melanoma cell growth.

CS-891 may effectively treat hair loss by blocking enzymes in hair follicles.

Satoyoshi syndrome can occur without causing premature ovarian failure.

Adipose-derived stem cells can help repair tissue in lipodystrophy patients.

Thymic transplantation normalized some T-cells but not others, maintaining immune function.

TCF/Lef1 activity is essential for proper skin cell development and renewal.

ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

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

Antisense oligonucleotides show promise for treating Myotonic Dystrophy type I.