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Croton membranaceus root extract can change how drugs are processed in the body.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

CXXC5 can both suppress and promote cancer, making it a complex target for treatment.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

The decision tree can predict drug absorption issues with good accuracy but needs more validation and adjustments for other factors.

New mutations in the EBP gene cause CDPX2, affecting bones, skin, eyes, and hair, with females generally less affected than males.

Different mutations in the 5 alpha-reductase-2 gene were found in affected individuals in the Dominican Republic, suggesting no common ancestry.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

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

The rs1128977 gene variant may affect cholesterol and body measurements.

Methylated gene parts may cause finasteride-resistance in some enlarged prostate patients.

Researchers found a non-functional sheep keratin gene due to mutations.

Not having enough cystatin M/E protein causes less hair growth and dry skin.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

Low-penetration genes might help personalize colorectal cancer prevention.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

CYLD mutations cause a variety of skin tumors with symptoms starting around age 16, and treatments are currently limited.

Screening for the NUDT15 gene variant can prevent severe side effects from thiopurine drugs in East-Asian people.

Genetic factors in PCOS are complex, with potential influences from the MC4R gene.

CDP is crucial for lung and hair follicle cell development.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

Certain gene variations in the Vitamin D Receptor are linked to higher risk of female hair loss.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.

Certain gene variations increase the risk of alopecia areata in Koreans.

Lack of a key enzyme causes severe skin issues and death in mice.

The method accurately measures cyproterone acetate in plasma, showing no significant difference between two formulations.

Certain gene variations are linked to severe acne in Egyptian patients and could guide treatment choices.