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An Australian with rare hair loss and eye conditions had a gene linked to both, not seen together before.

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

There is no cure for myotonic dystrophy type 1, so treatment focuses on managing symptoms and complications.

The research found that a specific gene mutation causes fewer hair follicles and disrupted hair growth cycles, leading to thin and short hair in people with Hypotrichosis with Juvenile Macular Dystrophy.

Certain mouse strains develop a skin condition similar to a human hair loss disease due to genetic defects.

Myotonic Dystrophy may age cells faster, and drugs that target aging could be potential treatments.

Light can turn on hair growth cells through a nerve path starting in the eyes.

P-cadherin is important for hair growth and health, and its problems can cause hair and skin disorders.

Using CRISPR for gene editing in the body is promising but needs better delivery methods to be more efficient and specific.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

The document concludes that an experimental drug may help wound healing in Epidermolysis Bullosa, links Hydroa vacciniforme to EBV, discusses diagnosing hair loss disorders, finds many children with eczema have allergies, reviews the safety of a skin medication in children, notes side effects of a Duchenne's treatment, and identifies a marker for pediatric mastocytosis.

Japanese researchers created new hair follicles from human cells that grew hair when put into mice, and other findings showed a link between eye disease severity and corneal thickness, gene mutations affecting hearing and touch, and the safety of the shingles vaccine for adults over 50.

The ABCA4 gene protects hair follicle stem cells from toxic vitamin A byproducts.

Different types of cells in the eye express specific keratins at various stages of development.

Vitamin A is important for healthy skin and hair, influencing hair growth and skin healing, but UV light reduces its levels.

Frizzled receptors are essential for various body development processes and maintaining certain body functions.

WNT10A mutations often cause ectodermal dysplasias, with males showing more tooth issues than females.

Small molecule drugs show promise for advancing regenerative medicine but still face development challenges.

Diabetes often causes various skin problems and complications.

Altered retinoid metabolism in cicatricial alopecia suggests a balanced vitamin A diet may prevent the condition.

Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

Oral retinoids are effective for severe skin conditions but require careful use due to side effects.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

The study aims to find the best treatment for central serous chorioretinopathy by comparing various options.

New partnerships, clinical trials, and drug approvals marked progress in therapeutic delivery in July 2018.

Alopecia areata causes sudden hair loss, has genetic links, and can be managed but not cured.

Vitiligo is a skin condition causing white spots, more common in women, often starts before age 20, and can affect mental health.

Photobiomodulation therapy using red and near-infrared light can reduce inflammation and aid in healing various conditions.

Alopecia Areata is an autoimmune condition causing hair loss with no cure and treatments that often don't work well.

JAK inhibitors are effective in treating various immune-related diseases, not just rheumatoid arthritis.