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A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

Visceral leishmaniasis can mimic rheumatoid arthritis symptoms, especially in immunocompromised patients.

Analog 23 is a promising compound for prostate cancer treatment.

Adjusting the medication tacrolimus resolved a boy's red nail beds after a stem cell transplant.

A specific DNA duplication in Polish chickens affects feather shape by altering gene expression.

Certain genes are linked to the risk of developing Alopecia Areata.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

Some prostate cancers have gene changes that may affect treatment with certain drugs.

A boy with severe Vitamin D-resistant rickets did not respond to treatment and lacked a common symptom, suggesting a need for alternative treatments.

ATR-FTIR spectroscopy could help monitor alopecia areata treatment response non-invasively.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

Reporter characteristics affect detection of hair loss from cancer therapy.

Abatacept may help some people with alopecia areata regrow hair.

Burdock has potential for new pharmaceutical products due to its medicinal properties.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

Longer CAG repeats in gene linked to more severe hair loss in females.

KRTAP2-3 could help predict cancer recurrence by identifying specific cancer cells.

Arsenic trioxide effectively treats APL, improving survival rates despite its toxicity.

About 50% of 46, XY DSD cases lack a genetic diagnosis, but advanced sequencing methods improve detection.

A new gene mutation causes insulin resistance in a girl and her mother.

Raltitrexed conjugates are less potent than the free drug but more effective at high concentrations.

SQSTM1 is linked to increased risk of alopecia areata.

MX1 and AR genes are linked to milder COVID-19, while TMPRSS2 increases severe risk, especially in women.

RDW can be a useful marker for inflammation in alopecia areata patients.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

PRAME helps distinguish between benign and malignant skin cells in most cases.

Some human genetic markers work for genetic studies in pig-tailed and stump-tailed macaques, which can help in their conservation.

A mycobacterial protein shares a similar region with a human skin protein, possibly affecting skin diseases.

SMR-2 and SMR-6 are much more toxic than retinoic acid, causing severe symptoms and organ damage in mice.

The androgen receptor gene doesn't help identify women likely to have female pattern hair loss.