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The research identified and described a gene important for hormone conversion in endangered catfish, which varies in activity during different reproductive stages and after hormone treatment.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

GLP-1 receptor agonists may help manage and prevent diabetic foot ulcers.

GFP transgenic mice help study cell origins in skin grafts.

Ac-GFFY-IGF peptide is a promising, safe, and effective treatment for hair loss, better than current options.

Large-scale reconstructions enhance understanding of vibrissal sensory mapping in the brain.

Versican in dermal papilla cells is crucial for healthy hair growth.

A new genetic disorder caused by an ODC1 mutation can be treated with DFMO.

Gene therapy with the Math1 gene helped regenerate balance-related cells and improve balance in mice.

Connexin-26 gene mutations may increase cancer risk in KID syndrome patients.

Dopaminergic neurons in the gut have diverse subtypes with different neurotransmitter contents.

Changes in genes FGA, VWF, and ACTG1 may contribute to pemphigus vulgaris.

rPanglaoDB helps study rare cell types by merging RNA data, showing fibrocytes aid in healing.

The LTF gene may help predict and manage nonspecific orbital inflammation.

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

A new genetic mutation causing Xeroderma Pigmentosum was found in an 8-year-old girl, affecting her DNA repair.

Pemphigus vulgaris involves specific immune cells and B cells that produce antibodies causing skin blisters.

A stable sheep ovarian cell line was created for studying reproduction and hormones.

Cannabidivarin (CBDV) may help brain cell growth and survival through the TRPV1 receptor.

Graft-versus-host disease occurs when donor immune cells attack the recipient's body, causing skin, gut, and liver damage.

Involucrin is crucial for skin cell maturation and protection.

Female donor to male recipient sex mismatch and positive ACA-IgG are key risk factors for vitiligo and alopecia areata in chronic GvHD patients.

Suppressing the HGPS mutation may improve symptoms and suggest reversibility.

Provenge extends prostate cancer survival by about 4 months.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

High glycine–tyrosine keratin-associated proteins help make hair strong and maintain its shape.

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.

Desmoglein 3 organization in cell connections changes without calcium, affecting cell adhesion.