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Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.

The research showed that CRISPR/Cas9 can fix mutations causing a skin disease in stem cells, which then improved skin grafts in mice, but more work on safety and efficiency is needed.

The conclusion is that differentiating wound types in RDEB patients is important for clinical trials and understanding the disease.

The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.

The document concludes that ERBB2 mutations are common in extramammary Paget disease and may respond to systemic treatments like cancer immunotherapy.

Targeted therapy with Ustekinumab significantly improved a skin condition called ILVEN, which is caused by mutations in the CARD14 gene.

Golden oyster mushroom extract may protect skin cells from aging by its antioxidant properties.

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

Understanding skin structure and development helps diagnose and treat skin disorders.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

Intralesional chemotherapy with 5-fluorouracil and methotrexate may worsen keratoacanthoma-type skin cancer in transplant patients.

Most Recessive Dystrophic Epidermolysis Bullosa patients with a specific mutation likely have Sephardic ancestry from about 500 years ago.

A specific gene mutation causes a severe skin disorder in a family.

Certain genes in Iranian sheep are linked to wool production and heat adaptation.

New treatments for ichthyosis, like protein replacement and gene therapy, show promise and may become standard care.

Certain genes are linked to the quality of cashmere in goats.

Aging reduces skin stem cell function, leading to changes like hair loss and slower wound healing.

FKBP10 and FBN2 are key proteins for hair growth in cashmere goats.

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

The Wnt/β-catenin pathway is important for body functions and diseases, and targeting it may treat conditions like cancer, but with safety challenges.

The research provides a gene-based framework for hair biology, highlighting the Hippo pathway's importance and suggesting links between hair disorders, cancer pathways, and the immune system.

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

A specific mutation known for causing cancer is also found to cause a skin condition in a young girl.

The protein aPKCλ is crucial for keeping hair follicle stem cells inactive and for hair growth and regeneration.

Different types of skin cells have unique genetic markers that affect how likely they are to spread cancer.

A specific RNA molecule, circCOL1A1, affects the growth and quality of goat hair by interacting with miR-149-5p and influencing cell growth pathways.

A new MBTPS2 gene variant disrupts fat metabolism and collagen production, causing Osteogenesis imperfecta.

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

JAGGED1 could help regenerate tissues for bone loss and heart damage if delivered correctly.

The Rotterdam Study found risk factors for elderly diseases, links between lifestyle and genetics with health conditions, and aimed to explore new areas like DNA methylation and sensory input effects on brain function.