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The skin protects the body and is constantly renewed by stem cells; disruptions can lead to cancer.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.

Niosomes are promising for skin drug delivery, offering benefits like improved drug penetration and stability.

S100A4 and S100A6 proteins may activate stem cells for hair follicle regeneration and could be potential targets for hair loss treatments.

Overexpressing the mineralocorticoid receptor in mouse skin causes skin thinning, early skin barrier development, eye issues, and hair loss.

Noggin overexpression delays eyelid opening by affecting cell death and skin cell development.

Coffee silverskin may be a beneficial and safe ingredient for cosmetics, offering hydration, firmness, and potential hair growth benefits.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

The extracellular matrix is crucial for controlling skin stem cell behavior and health.

Burn reconstruction improves with new techniques, materials, and tissue engineering.

Mice with human skin protein K8 had more skin problems and cancer.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

The article concludes that advancements in hair cosmetics require dermatologists to stay informed about products and their potential risks, including allergies and higher risks for hairdressers.

Some hair loss disorders are caused by genetic mutations affecting hair growth.

Ephrins slow down skin and hair follicle cell growth.

Tiny particles called extracellular vesicles could help with skin healing and hair growth, but more research is needed.

Transit-amplifying cells are crucial for tissue repair and can contribute to cancer when they malfunction.

Certain medications and patient factors increase the risk of Intraoperative Floppy Iris Syndrome during cataract surgery, but with careful planning and technique adjustments, complications can be minimized.

Certain human skin cells marked by CD44 and ALDH are rich in stem cells capable of long-term skin renewal.

Lash ptosis is more common and severe in people with congenital eyelid droop than in those with acquired eyelid droop or without eyelid droop.

The study found no common cause for a girl's crystalline cataract and uncombable hair, suggesting their co-occurrence might be coincidental.

The research suggests that a specific skin gene can be controlled by signals within and between cells and is wrongly activated in certain skin diseases.

A boy with chromosome 13q deletion syndrome developed eye cancer, a woman with breast cancer lost vision due to a rare side-effect of her treatment, a man's vision worsened after using a hair loss drug, and two rare disorders were discussed. Optical Coherence Tomography is useful for diagnosing and monitoring these conditions.

Stem cell differentiation is crucial for skin barrier maintenance and its disruption can lead to skin diseases.

Eye exams are crucial for kids with 13q deletion syndrome, tamoxifen can cause vision loss, Propecia may lead to cataracts, Lipoid Proteinosis causes skin bumps, and OCT is useful for diagnosing macular diseases.

New chemotherapy drugs cause skin side effects, but treatments like minocycline and tetracycline can help reduce them.

Newer skin resurfacing lasers reduce damage and scarring, with some approved for safe use and minimal side effects.

Non-thermal plasma treatment makes mouse skin thicker and increases growth factors without harming the tissue.

Brazilian propolis was found to speed up hair growth in mice by increasing the growth of skin cells that form hair.

A 15-year-old with KID syndrome developed a rare skin condition called PEHFN.