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The 1298CC genotype in RA patients leads to higher methotrexate toxicity, while the 1298AA genotype results in better treatment response.

Circular RNA ERCC6 helps activate stem cells important for cashmere goat hair growth by interacting with specific molecules in an m6A modification-dependent way.

Genetic mutations that disrupt homocysteine breakdown lead to increased damage in mouse hair keratin.

Caribine from traditional Chinese medicine may help treat hair loss.

Hair follicle samples effectively show how well the drug MK-0752 targets and engages with the Notch pathway.

The laser system helps study brain cell functions by precisely removing specific cells and observing changes.

The study concluded that the arachidonic acid pathway and the protein KRT79 play a role in determining the fineness of cashmere.

HT-scCAT-seq helps understand gene regulation in embryonic skin development.

Substance from human umbilical cord blood cells promotes hair growth.

Lipid-antigen stimulation may play a role in folliculotropic mycosis fungoides.

Method accurately measures finasteride concentration in medicine.

A new genetic variant causes BRESHECK syndrome by disrupting cell growth and stress response.

A mutation in the hHb3 gene is linked to the hair disorder monilethrix.

Low m6Ascores in melanoma predict better survival and response to immunotherapy.

Introducing the rat OTC gene normalized hair growth in SPF-ASH mice.

The wavy coat in NCT mice is caused by multiple genes, including a mutation in the Prss53 gene.

PROTACs offer new ways to treat hard-to-target diseases, with promising drugs for cancer in advanced trials.

A patient with a larger than usual genetic mutation had a broader range of symptoms for a muscle disease.

A new method was developed to make a compound used in finasteride and epristeride with a 69% yield.

A mutation in the KRT86 gene causes hair fragility in a Turkish family.

The AMHR2-482A>G gene change is linked to higher PCOS risk.

Targeting adipocyte-to-mesenchymal transition could help treat fibrosis.

Long-read RNA sequencing can identify complex gene changes in IFAP syndrome.

Osteopathic manipulation therapy might help treat dementia caused by finasteride.

The enzyme is crucial for skin cell development and can be activated without proteolytic activation.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

Mutations in mitochondrial DNA might significantly contribute to the development of Polycystic Ovarian Syndrome.

Researchers used CRISPR/Cas9 to create a goat with a gene that increased cashmere production by 74.5% without affecting quality.

Researchers developed a new method using methylene blue staining to more accurately identify the growth stage of human hair follicles.

The treatment increased total hair count but wasn't significantly better than placebo.