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Phosphorylation controls TFEB's location in the cell, affecting cell metabolism and stress response.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

Blocking SEPT4 might help heal wounds and regrow hair faster.

Mutations in the spike protein affect drug binding and effectiveness.

The new wound dressing improves healing and tissue repair better than conventional dressings.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

Blocking the Mitochondrial Pyruvate Carrier causes stress in hair follicles, which can be reduced by an ISR inhibitor.

Deleting the Sox21 gene changes hair lipid composition and increases cholesterol sulfate levels.

EETs can delay seizures by affecting GABA activity, offering potential new treatments for seizures.

5alpha-reductase 2 is crucial for proper male brain development and sexual differentiation.

A certain genetic variation in the IL1A gene may lower the risk of a hair loss condition in Chinese people.

A mutant FERONIA gene affects root hair growth at high temperatures.

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

TMPRSS2 is crucial for COVID-19 infection and is a potential target for treatment.

MEF2C is crucial for normal hair cycle progression.

Overexpressing 14-3-3σ in mice skin reduces cell growth and hair density.

A mutation in the VDR gene affects hair cycling without needing ligand binding.

The enzyme sEH is important for hair growth and its inhibition could help treat hair loss.

Human and mouse TGase3 enzymes are similar but differ near the activation site, crucial for their function in skin and hair development.

The gene for slick hair in Senepol cattle is located on chromosome 20 and may involve the SRD5A2 gene.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

The study showed that a specific DNA sequence can control gene expression in hair growth areas of mice.

Loss of TET2 increases the risk of skin and oral cancer.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

ANE syndrome is caused by a mutation in the RBM28 protein that disrupts ribosome assembly.

Type 1/17 inflammation in psoriasis increases skin cell growth due to a molecule that could be a new treatment target.

A gene mutation in mice causes increased mast cells and disorganized hair follicles in their skin.

A new gene mutation causes complete androgen insensitivity in a 16-year-old with a female appearance.