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Zfp157 is active in many mouse tissues during development and in specific adult cells.

Glycated hemoglobin is not as effective as the oral glucose tolerance test for diagnosing blood sugar problems in women with PCOS in Southern Iraq.

Box A of HMGB1 can improve stem cell function, aiding anti-aging therapy.

New LSS gene variants help understand congenital hypotrichosis 14 better.

The prolactin gene polymorphism doesn't affect cashmere quality in these goats.

Ayme-Gripp Syndrome was confirmed in a woman through genetic testing, highlighting the need to consider rare genetic conditions in diagnoses.

New lipid/fiber microplexes improve mRNA therapy for degenerative diseases by enhancing cell function and treatment effectiveness.

Different γδ T cell types have unique roles in causing alopecia areata.

Loss of Pten in certain hair follicle stem cells increases skin cancer risk.

Gene variation affects prostate issues and hair loss.

Selective breeding caused the unique curly hair in Mangalitza pigs.

Sebaceous glands help study fatty acid transporters and binding proteins.

The FTO gene hinders stem cells in hair follicles from becoming pigment cells.

Injecting recipient splenocytes into donors' thymus can prevent graft-versus-host disease.

Sex steroids affect the MafB gene differently in male and female hamsters.

A gene called HDAC9 might be a new factor in male-pattern baldness.

GPR40 agonists help hair growth through the protein ANGPTL4.

Increasing PBX1 reduces aging and cell death in hair follicle stem cells by boosting SIRT1 and lowering PARP1 activity.

Transgender youth have more sleep disorders, but gender-affirming therapy may help reduce them.

GABEB is a less severe skin condition caused by a gene mutation affecting collagen, leading to blisters and other symptoms.

Late dumping syndrome after fundoplication can be diagnosed with an oral glucose tolerance test and managed with diet changes.

Mice with extra human KLK14 had hair and skin problems, including weaker cell bonds and inflammation, linked to Netherton syndrome.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

NCBP3, SDHA, and PTPRA are the best genes for accurate goat skin research.

Low-coverage sequencing is a cost-effective way to find genetic factors affecting rabbit wool traits.

Somatostatin analogues effectively manage ectopic ACTH syndrome when surgery isn't possible.

SFRP2 and PTGDS may be key factors in female hair loss.

Gingerol may help treat chronic graft-versus-host disease by improving immune cell balance.

Mutations in the KRT16 gene can cause skin and nail disorders.

A new genetic mutation in the CAST gene may link PLACK syndrome to alopecia areata.