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The research provides a gene-based framework for hair biology, highlighting the Hippo pathway's importance and suggesting links between hair disorders, cancer pathways, and the immune system.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

The HoxC gene cluster and its enhancers are essential for developing hair and nails in mammals.

The conclusion is that the nuclear lamina and LINC complex in skin cells respond to mechanical signals, affecting gene expression and cell differentiation, which is important for skin health and can impact skin diseases.

Chemotherapy and radiation therapy cause skin and hair damage by altering gene expression and signaling pathways.

The BMP/Smads pathway and Id2 gene control hair follicle stem cells, affecting their rest and growth phases.

Scientists found gene mutations that affect hair loss, skin stem cells, and skin disorders, and identified drugs that may help treat blood vessel and skin conditions.

Mutations in the androgen receptor gene cause different levels of androgen insensitivity, making it hard to create simple tests for the condition.

The AUTS2 gene is linked to neurological disorders and may affect human brain development and cognition.

A WNT10A gene mutation leads to ectodermal dysplasia by disrupting cell growth and differentiation.

A new gene, JMJD1C, may affect testosterone levels in men.

Mice with a Gsdma3 gene mutation have thicker skin and longer hair follicle openings due to increased β-catenin levels.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

The research shows that a gene called Wnt3 affects hair growth and structure, causing short hair and balding when overactive.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Scientists found a gene in mice that causes early hearing loss.

NcoA4 may have roles beyond helping control gene activity, possibly affecting cell behavior and stability.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Removing the ROBO4 gene in mice reduces skin inflammation and hair loss by affecting certain inflammation pathways and gene expression.

Deleting the p63 gene in certain cells causes problems in thymus development and severe hair loss in mice.

Ingenol mebutate gel changes gene expression related to skin development and immune response in actinic keratosis.

The E2 protein affects gene activity in hair follicles of mice.

Removing a specific gene in certain skin cells causes hair loss on the body by disrupting normal hair development.

Mice lacking the PPARγ gene in their fat cells had almost no fat tissue, severe metabolic problems, and abnormal development of other fat-related tissues.

A mutation in the Soat1 gene causes hair structure defects and other health issues in AKR/J mice.

A mutation in the Adam10 gene causes freckle-like spots on Hairless mice.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

The article concludes that better understanding gene regulation related to seasonal changes can offer insights into the mechanisms of seasonal timing in mammals.

Hair growth is controlled by specific gene clusters and proteins, and cysteine affects hair gene expression in sheep.