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A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

VDC-1101 shows potential as a treatment for canine cutaneous T-cell lymphoma.

Lampreys have a functional vitamin D receptor that may help detoxify harmful substances.

A child has a rare hair and skin disorder due to specific gene variants, suggesting broader genetic testing is needed.

Laminin 332 is essential for normal skin cell behavior and structure.

Cats with abnormal hair had DSG4 gene changes causing hair problems.

Scientists found a gene in mice that causes early hearing loss.

Tjalma Syndrome is a rare condition in people with lupus, causing fluid buildup and high CA-125 levels, but not due to tumors.

The nanocomposite effectively targets lung cancer cells without harming normal cells.

The transporter protein SH1446 in Staphylococcus hominis is key to underarm odor production.

Fadrozole and finasteride change gene expression related to sex hormones and thyroid hormones in frog larvae development.

Sodium valproate effectively controls petit mal seizures in children but is less effective for other types, with minimal side effects.

The L412F variant of TLR3 is linked to skin infections, more viral infections, and autoimmune issues.

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

A boy with a rare skin condition and kidney disease improved with cyclosporine after steroids failed, suggesting a new treatment approach.

SLCO genes may predict prostate cancer mortality risk, and lifestyle changes improve health in advanced prostate cancer.

The N363S gene variant does not cause higher adrenal androgen levels in women with polycystic ovary syndrome.

PRC2 is essential for maintaining intestinal cell balance and aiding regeneration after damage.

Researchers created a genetic library from a cashmere goat's skin and found new genes linked to hair growth.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

Arabidopsis Formin 2 stabilizes actin filaments to aid cell-to-cell trafficking.

The VEGF +405G allele may increase the risk of PCOS in South Indian women.

Lysocellin helps stop cell damage from etoposide and may prevent hair loss.

RSPO1 could help create new diabetes treatments by increasing pancreatic β cells.

Mouse skin cancer progression involves a unique group of cells marked by ABCG2 and MTS24.

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

Mutations in the enzyme don't significantly change how it binds to its specific substances.

Rapamycin and anti-EGFR antibody reduce LAM/TSC cell migration and blood vessel growth in the uterus.