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A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

The document suggests a possible link between FAM111B gene mutations and increased cancer risk, particularly pancreatic cancer.

Loss of a specific protein in skin cells causes symptoms similar to psoriasis.

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

People with Collagen VI-related myopathies may often have hair loss and scalp issues.

Overexpressing Dsg3 in mice skin causes excessive cell growth and abnormal skin development.

A disease causing skin issues in young adult German short-haired pointers is hereditary, with most affected dogs not responding to treatment.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

The document concludes that mouse models are crucial for studying hair biology and that all mutant mice may have hair growth abnormalities that require detailed analysis to identify.

Scalp biopsies from dermatomyositis patients show chronic hair loss without scarring, with mucin and blood vessel changes being very common.

Hidradenitis suppurativa is a chronic skin condition more common in women, linked to genetics and lifestyle factors, and associated with various other health issues.

Genetic defects and UV radiation cause skin damage and aging.

A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

The workshop highlighted the genetic links and psychological impacts of hair loss and skin disorders.

Obesity is linked to various skin problems and may increase the risk of skin cancer.

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.

People with Myotonic Dystrophy type 1 are more likely to have certain skin conditions, but not more likely to get skin cancer.

A Jordanian family with Clouston syndrome has a common GJB6 gene mutation.

Blocking IL-17 can reduce skin inflammation in a mouse model of pityriasis rubra pilaris.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

A gene called Gk5 controls lipid production in the skin and affects hair growth.

Testosterone can cause acne and male-pattern baldness, affects hair growth in men and women, and makes male skin more sensitive.

A girl with Becker's nevus syndrome showed good improvement in breast development using spironolactone.

Using special RNA to target a mutant gene fixed hair problems in mice.

Mutations in the KRT85 gene cause hair and nail problems.

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

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

Activin helps skin growth and healing mainly through stromal cells and affects keratinocytes based on its amount.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

Three new types of a skin blistering disease were found, caused by specific gene mutations.