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The transgene likely activated an oncogene or interrupted a tumor suppressor gene, causing melanoma in mice.

Researchers found that the Leptin receptor is a consistent marker for hair follicle dermal cells, which may help future hair research.

Effective treatments for spinal and bulbar muscular atrophy are not yet available; more research is needed.

Certain DNA regions in alpacas are linked to fiber diameter.

Wounded skin cells can revert to stem cells and help heal.

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

Understanding intermediate filaments helps explain hair health and related diseases.

CD201+ fascia progenitors are essential for wound healing and could be targeted for treating skin conditions.

Progeria, a disease that causes early aging, is linked to a gene mutation and helps us understand normal aging.

EGFR inhibitors cause skin issues and hair loss by weakening skin defenses, suggesting antibiotics and targeted treatments can help.

Scientists developed tools to observe hair regeneration in real time and assess skin health, using glowing mice and light-controlled genes.

Premature aging increases the risk of immune problems and autoimmune diseases.

New cells join the hair's dermal papilla during the growth phase, possibly affecting hair thickness.

Copper treatments increase copper in all tissues, but brindled female mice accumulate much more copper in their kidneys without clinical effects, unlike brindled male mice where brain copper deficiency is clinically significant.

Type 2 inflammation helps wound healing by switching immune cells to repair mode.

The document concludes that certain rats and mice are useful for studying hair loss in humans and testing treatments.

Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.

Gene therapy, especially using atoh1, shows promise for creating functional sensory hair cells in the inner ear, but dosing and side effects need to be managed for clinical application.

Wnt proteins from certain skin cells are crucial for normal hair growth and renewal.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

New treatments for hair loss from alopecia areata may include targeting immune cells, using stem cells, balancing gut bacteria, applying fatty acids, and using JAK inhibitors.

The document updated knowledge on skin disorders, focusing on unusual moles in older adults, the progression from moles to melanoma, and evolving hair loss treatments.

Melanoma risk tools need improvement, a gene mutation causes a hair disorder that might be treated by managing cell stress, a potential therapy for a skin-ear disorder involves blocking cell channels, skin wrinkling may indicate lung aging regardless of smoking, and oxidative stress might contribute to common baldness.

Researchers discovered potential origins and new treatments for skin cancer, including biomarkers for melanoma and therapies that reduce tumor growth.

Half of people with Alopecia Areata may see hair regrowth within a year without treatment, but recovery is unpredictable.

Alopecia areata is an autoimmune disease where T cells attack hair follicles.

Planarian regeneration begins with a specific gene activation caused by injury, essential for healing and tissue regrowth.

The hedgehog signalling pathway is key in skin development and basal cell carcinoma, offering insights for prevention and treatment.

Alopecia areata is an autoimmune condition causing hair loss due to the immune system attacking hair follicles, often influenced by genetics and stress.

Periodontal ligament stem cells show promise for regrowing tissues but require more research for safe, effective use.