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A new gene mutation causes vitamin D resistance and hair loss in two unrelated girls.

Spt4 and Spt6 are essential for fat cell development.

Breast cancer treatments work better with AR activation, improving results and reducing side effects.

Prostaglandin E2 helps prevent hair loss from radiotherapy by protecting hair cells.

Hairless protein helps control hair growth by regulating vitamin D receptor activity.

Oral contraceptive use may increase the risk of frontal fibrosing alopecia in women with a specific CYP1B1 gene variant.

LPA3 signaling in the uterus is crucial for placental formation and fetal development.

Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.

Pigs without the Hairless gene showed skin and thymus changes, useful for studying human hair disorders.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

Researchers created a new light source that improves chemical imaging by removing background noise.

LTBP1 is a key regulator in diseases and a potential target for new treatments.

The thulium laser and PDRN injections effectively improved hair thickness in patients with pattern hair loss.

The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

A new genetic mutation in the TRPV3 gene causes Olmsted-like syndrome in a Mongolian family.

A rare skin condition in a 17-year-old was diagnosed late, stressing the need for careful evaluation and genetic testing.

Certain genetic variants in keratins increase the risk of tooth decay.

Everyone has an immune response to PPD, but reactions differ, causing tolerance, mild inflammation, or allergy.

During late pregnancy in rats, hormonal changes increased certain GABAA receptors in specific brain cells.

CLE14 peptide promotes root hair growth in Arabidopsis.

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

Certain genes control the color of human hair by affecting pigment production.

EDA2R is a key gene linked to ageing and diseases, and targeting it may help treat conditions like hair loss and chronic diseases.

The Thr1022Ala variant in the hairless gene is not a disease-causing mutation.

Truncated LTBP-1 disrupts TGF-β signaling, affecting hair growth.

Prostaglandins and the enzyme AKR1C3 could play a role in skin cancer and hair loss, and further research is needed to understand these mechanisms.

Overexpression of PKCepsilon leads to increased TNFalpha, promoting metastatic squamous cell carcinoma in mice.