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A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

Two siblings have a rare hair condition caused by a new genetic variant.

The FDA did not approve certain drugs for prostate cancer prevention due to concerns about their effectiveness and potential risks.

Low TRPS1 expression in skin and hair cells is linked to hair problems in Trichorhinophalangeal syndrome.

BLTP1 and KIF27 gene mutations can help breed better wool sheep.

Type 3C diabetes is a distinct condition needing more research and treatment strategies.

New gene variants were found for rare skin and hair disorders, improving understanding and treatment.

Drugs that block GSK-3 show promise for treating various diseases.

H1 increases risk for neurodegenerative diseases, while H2 offers protection but is linked to other disorders.

A new genetic mutation in the hairless gene causes a rare hair loss disorder.

Aggressive immunosuppressive treatment improved a woman's severe heart condition linked to autoimmune disease.

The risk of skin tumors becoming malignant depends on the specific skin cell type affected.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

MT-DADMe-ImmA can selectively kill head and neck cancer cells without harming normal cells.

A specific gene mutation causes severe skin and nail issues and hair loss.

TRM21 helps control flavonoid production and root hair growth in Arabidopsis thaliana.

Somatic BHD mutations are rare in Japanese renal tumors.

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

The MtAnn3 gene affects root hair growth and is influenced by cytokinin.

Melanocyte pathology requires keratinocyte hyperplasia and regulation dysfunction.

The PML protein helps prevent skin cancer in mice.

Mutations at Val-889 and Arg-752 disrupt key interactions in the androgen receptor, affecting its function.

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

Mutation in hairless gene may increase hair loss risk.

Too much Smad7 can cause serious changes in skin tissues, including problems with hair growth, thymus shrinkage, and eye development issues.

Mutation in hairless gene may increase hair loss risk.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

EGFR deficiency in skin causes hair follicle issues and inflammation.

Allopregnanolone changes gene expression in glioblastoma cells.