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Understanding how epigenetic regulation affects stem cells is key to cancer insights and new treatments.

Understanding how acne develops in different diseases could lead to new treatments.

A patient with myotonic dystrophy had several autoimmune disorders and thyroid cancer, suggesting a possible link between these conditions.

A patient with untreated congenital adrenal hyperplasia had large benign tumors in her adrenal glands removed, improving her symptoms.

Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.

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.

Certain mature cells in mouse lungs can turn back into stem cells to aid in tissue repair.

E211 G>A gene linked to lower risk of severe prostate cancer and hair loss.

Stem cell niches are adaptable and key for tissue maintenance and repair.

CYLD mutations cause a variety of skin tumors with symptoms starting around age 16, and treatments are currently limited.

Hormones during pregnancy and lactation keep skin stem cells inactive, preventing hair growth.

Vitamin D3 analogs can promote hair growth in mice genetically prone to hair loss.

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

Mutations in the WNT10A gene can cause skin, hair, teeth, and other disorders, and may also affect other areas like kidney and cancer, with potential for targeted treatments.

Future research on ectodysplasin should explore its role in diseases, stem cells, and evolution, and continue developing treatments for genetic disorders like hypohidrotic ectodermal dysplasia.

A boy with Sjogren-Larsson syndrome has skin and muscle symptoms due to a specific enzyme deficiency.

A 23-year-old woman with Hashimoto’s thyroiditis improved significantly after a 15-month integrative treatment plan.

Faulty inflammasome activation may lead to autoimmune skin diseases and could be a target for new treatments.

Estrogen and androgenic hair increase melanoma risk, especially in European-ancestry individuals.

The lotion and shampoo effectively treated scalp seborrheic dermatitis.

Nuclear shape and chromatin changes affect gene expression in skin cell differentiation.

The symposium highlighted the importance of understanding disease mechanisms for targeted dermatology treatments.

Hair growth-related cells need the enzyme SCD1 to help maintain the area that supports hair growth.

Patients with RASopathies have a higher risk of autoimmune disorders and should be routinely screened.

Non-classic congenital adrenal hyperplasia (NCCAH) can mimic PCOS and requires genetic testing for proper diagnosis and treatment.

Acne is linked to inflammation and insulin resistance, and is associated with various syndromes that require different treatments.

The document concluded that stem cells are crucial for skin repair, regeneration, and may help in developing advanced skin substitutes.

Blond hair in Solomon Islanders is due to a unique genetic variant, not European ancestry.

Removing the ATR gene in adult mice causes rapid aging and stem cell loss.

Changing the environment around stem cells could help tissue repair, but it's hard to be precise and avoid side effects.