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A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

Metabolic signals and cell shape influence how cells develop and change.

New therapies are being developed that target integrin pathways to treat various diseases.

PAI-2 helps in the maturation and protection of hair and nail cells.

Notch signaling disruptions can cause various skin diseases.

Clim proteins are essential for maintaining healthy corneas and hair follicles.

Citrullinated proteins from Porphyromonas gingivalis may contribute to rheumatoid arthritis.

Hair is important for protection, social interaction, and temperature control, and is made of a growth cycle-influenced follicle and a complex shaft.

Laminin 332 is essential for normal skin cell behavior and structure.

When skin blisters, healing the wound is more important than growing hair, and certain stem cells mainly fix the blisters without helping hair growth.

Integrin β1 is crucial for liver structure and function, preventing fibrosis.

Cell polarity signaling controls tissue mechanics and cell fate, with complex interactions and varying pathways across species.

SCD1 is important for hair growth by keeping the connection in skin cells where hair stem cells live stable.

ZO-1 helps hair follicle stem cells renew better by changing their structure.

Human hair keratin might be good for filtering out harmful substances from water.

Mechanical force is important for the first contact between skin cells and hair growth in mini-organs.

The document concludes that managing Dunnigan-Type Familial Partial Lipodystrophy involves treating associated health issues and using medications like metformin and leptin replacement.

Laminin-511 is crucial for early hair growth and maintaining important hair development signals.

The document says that treating the root cause of hair follicle damage is crucial to prevent permanent hair loss, and treatment options vary.

Mechanical forces are crucial for shaping cells and forming tissues during development.

The document concludes that permanent hair loss conditions are complex, require early specific treatments, and "secondary permanent alopecias" might be a more accurate term than "secondary cicatricial alopecia."

t-Flavanone helps improve male pattern hair loss by making hair roots stronger.

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

Bidirectional barbed sutures are effective and can reduce surgery time, with a low infection rate and potential cost savings despite being more expensive.

New treatments and diagnostic methods for various animal skin conditions showed promising results.

A 3-month stay in space causes skin thinning, disrupts hair growth, and changes muscle-related genes in mice.

Dermoscopy is useful for diagnosing various skin, hair, and nail disorders and can reduce the need for biopsies.

The document concludes that inherited epidermolysis bullosa is a challenging genetic condition requiring multidisciplinary care and new treatments.

Parkinson's disease is linked to skin disorders and skin cells help in studying the disease.

A gene deletion causes the "hairless" trait in Iffa Credo rats.