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Ranitidine and finasteride lower TMAO levels, reducing heart and kidney damage by changing gut bacteria.

A boy's growth and immune problems were caused by a new mutation in the STAT5B gene.

A new mutation in the HR gene causes hair loss in a specific family.

The research found that a complex gene network, controlled by microRNAs, is important for hair growth in cashmere goats.

KAP8.1 gene variations affect cashmere weight in Inner Mongolian goats.

Bacteria in our hair can affect its health and growth, and studying these bacteria could help us understand hair diseases better.

Human prenatal skin develops an immune network early on that helps with skin formation and healing without scarring.

Women with nonclassic congenital adrenal hyperplasia experience more sexual dysfunction and distress.

Removing a methyl group from the ITGAV gene speeds up bone formation in a specific type of bone disease model.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

Quercetin significantly helps hair growth by activating hair follicles and improving blood vessel formation around them.

The document concludes that the human keratin gene cluster is complex, with a need for updated naming to reflect over 50 functional genes important for hair and skin biology.

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.

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

Keratin genes change gradually during skin cell development and should be used carefully as biomarkers.

3D culture helps maintain hair growth cells better than 2D culture and identifies key genes for potential hair loss treatments.

Researchers identified genes and proteins that may influence wool thickness in sheep.

A new mutation in the STS gene causes X-linked ichthyosis, even in rare female cases.

The FAT1 gene and its variations can help improve wool quality in Chinese Merino sheep through selective breeding.

Hairless mice are more vulnerable to Listeria infection, but gut microbiota can help reduce damage.

Frontal Fibrosing Alopecia is a poorly understood condition that is hard to treat and causes distressing hair loss.

The patient's hair was thinner and had fewer lipids due to a genetic mutation.

A new gene mutation may allow some piebaldism patients to regain skin color in white patches.

People with alopecia areata have higher levels of RBP4 protein and antibodies against it.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

The EDAR gene mutation leads to thinner and more deformed hair shafts.

Maize hybrids show better early growth due to complex gene interactions from their parent strains.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

Early intervention with JAK inhibitors may prevent alopecia areata progression.

Remote photobiomodulation improves brain injury outcomes and behavior in rats.