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A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Celsr1 is crucial for skin cell alignment, while Celsr2 has little effect on this process.

A genetic marker linked to a type of hair loss was found in most patients studied.

Keratin is crucial for keeping skin cells healthy and its changes can lead to diseases and affect cell behavior.

Harlequin mutant mice have hair loss due to low AIF protein levels and retroviral element activity.

Genetically modified sheep with more β-catenin grew more wool without changing the wool's length or thickness.

KGF and its receptor are found in enlarged prostate tissue and KGF strongly increases cell growth.

A specific RNA molecule, circCOL1A1, affects the growth and quality of goat hair by interacting with miR-149-5p and influencing cell growth pathways.

A specific RNA modification in cashmere goats helps activate hair growth-related stem cells.

Hyaluronic acid and versican are important for skin healing and hair growth and might help in regenerative medicine.

Kir6.1 mutations in Cantú syndrome increase channel sensitivity and hyperpolarization, while SUR2B mutations do not.

Scientists made a sensor that can detect a specific type of RNA related to androgen receptors quickly and accurately.

Keratin 18 helps diagnose and predict cancer progression and affects cancer growth and spread.

Pilose antler extracts help hair growth by activating hair follicle stem cells.

Combining genetic and physical trait analysis improves diagnosis accuracy for monogenic diabetes.

CCDC22 and CCDC93 are essential for root and root hair growth in Arabidopsis.

Researchers found that certain RNA sequences play a role in yak hair growth and these sequences are somewhat similar to those in cashmere goats.

The meeting highlighted the genetic basis of female pattern hair loss and various skin health insights.

Ovol2 is crucial for hair growth and skin healing by controlling cell movement and growth.

Gene therapy shows promise for healing chronic wounds but needs more research to overcome challenges.

Scientists are still unsure what triggers the immune system to attack hair follicles in Alopecia areata.

Mutations in NIPAL4 cause skin issues by disrupting lipid layers, but some improvement is seen with topical treatment.

Enzymes are classified into six types and are essential for many biological processes, with only a few targeted by drugs.

The JAK/STAT pathway is important in cell processes and disease, and JAK inhibitors are promising for treating related conditions.

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

SSAT is a key enzyme affecting cell growth and metabolism, with potential but risky use in disease treatment.

More precise, personalized therapies are needed for autoimmune diseases.

The absence of functional sebaceous glands causes hair follicle destruction and scarring alopecia.

Overexpressing follistatin in mice delays wound healing and reduces scar size.

Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.