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A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

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

Folliculotropic mycosis fungoides has unique molecular features and cell interactions that could guide targeted therapy.

The MLPH gene is not linked to seasonal hair loss in Rhodesian Ridgeback dogs.

A gene mutation in mice causes skin defects and early death.

Most children with a common hemochromatosis genotype had elevated iron levels but no severe symptoms.

DNMT3A is crucial for healthy skin and hair growth.

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

HtrA2 activity is crucial for normal hair growth by regulating fat cell development.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

A certain genetic variation is linked to a higher risk of polycystic ovarian syndrome.

MLO proteins help regulate calcium and ROS levels, promoting root hair growth in Arabidopsis.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

Aromatase gene variation may increase female hair loss risk.

m6A methylation affects the thickness of Alpine Merino wool fibers.

Mitochondrial Complex I reduces inflammation and increases bone breakdown by affecting certain immune cells.

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

These specific gene polymorphisms are not linked to Alopecia Areata in Egyptians.

The study found two new mutations in a Chinese patient with severe biotinidase deficiency.

A boy with a rare form of early puberty caused by a new gene mutation responded well to treatment aimed at reducing testosterone and preserving adult height.

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

Frontal fibrosing alopecia is linked to four genetic areas, especially the HLA-B*07:02 allele.

A new mutation in the HJV gene was found in a young woman with juvenile hemochromatosis, causing unusual symptoms like secondary hypothyroidism.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

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

Hidradenitis suppurativa may be more severe in people with Mediterranean fever gene mutations.

Deleting the Trf1 protein in mice is safe and may help prevent cancer without major side effects.

Maternal melatonin improves offspring hair growth by affecting specific proteins and pathways.

Methionine restriction works better than betaine for treating CBS deficiency symptoms in mice.

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