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The workshop discussed the role of a protein called calreticulin in health and disease, its potential as a treatment target, and its possible use as a disease marker.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

ASLAN004 was safe and well-tolerated, supporting further development for treating certain diseases.

Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

Wnt proteins from certain skin cells are crucial for normal hair growth and renewal.

Phospholipase C-δ1 is crucial for normal hair development.

Ptprq has multiple forms that change during inner ear development.

Beta-catenin boosts hair follicle cell growth by increasing c-myc expression.

Caspase-14 is important for skin and hair development in all mammals.

Stat3 affects skin cancer development by altering keratinocyte stem cell behavior.

KY19382 helps regrow hair and create new hair follicles.

Basonuclin 1 (BNC1) helps skin cells multiply and move, which is crucial for wound healing.

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.

A gene mutation in mice causes permanent hair loss and skin issues.

FoxN1 gene is crucial for proper thymus structure and normal skin appearance.

Beta-catenin is crucial for skin cell growth, development, and cancer formation.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

SHISA6 helps maintain certain stem cells in mouse testes by blocking signals that would otherwise cause them to differentiate.

Wnt/β-catenin signaling is important for keeping skin cell attachment structures stable.

The L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.

A new gene mutation is linked to monilethrix in the studied family.

Deleting the CD271 gene in mouse skin cells leads to disorganized skin and increased hair growth, suggesting CD271 is important for skin health.

Hoxc8 gene helps start mammary gland development by controlling specific signals.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

Only one K16 gene on chromosome 17 makes a functional keratin protein.

A virus protein can activate a pathway that may lead to abnormal hair follicle development.

Boosting β-catenin signaling in certain skin cells can enhance hair growth.