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Mesenchymal stem cells from laser-assisted liposuction are as effective and safe as those from conventional methods for cell therapy.

Lhx2 is essential for effective Sonic Hedgehog signaling in early retinal development.

Folliculotropic mycosis fungoides can affect the central nervous system in advanced stages.

Loss of the p53 gene alone causes tumors, and losing both p53 and Rb genes speeds up aggressive skin cancer.

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.

PLAU and SerpinB2 affect cell death differently in various forms of leprosy and could be targets for new treatments.

Patients with Systemic Sclerosis have much higher levels of GDF-15, which could help predict organ involvement and guide treatment.

SPRY1 deficiency in skin cells causes stem cells to move to the skin surface, leading to increased pigmentation.

αMSH may help regulate immune responses in hair follicles and its disruption could lead to hair loss.

Scarred skin in lichen planopilaris loses immune cells due to a decrease in a specific protein in skin cells.

Atg5 can promote tumors when autophagy is deficient but suppresses them under normal conditions.

Targeting lipid metabolism can help treat advanced, resistant cancers.

Transcutaneous vaccination using nanoparticles can enhance immune responses and reduce basal cell carcinomas.

The patient with both scarring and non-scarring hair loss showed complex immune reactions and improved with steroid treatment.

A rare skin condition in a baby showed unusual fat and hair follicle changes.

A specific type of immune cells, called CD301b-expressing macrophages, are crucial for skin repair processes.

There is no standard treatment for the rare Cronkhite–Canada syndrome, which can be fatal and lead to cancer.

Arab APS1 patients have unique and recurrent AIRE gene mutations.

Dynlt3 is important for melanosome transport and skin coloration.

Deleting MED1 in skin cells causes hair loss and skin changes.

Chronic cutaneous lupus erythematosus should be considered when acne treatments don't work.

New genes linked to male pattern baldness were found on chromosome 20p11.

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.

A woman's long-term scalp issues were diagnosed as a rare skin disorder called cutaneous Langerhans cell histiocytosis.

CLASI is a valid tool for assessing skin activity and damage in lupus patients.

HLA-DRB5 and other genes may be linked to alopecia universalis.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

A multidisciplinary approach is essential for effectively managing cutaneous lupus erythematosus.

Increased ODC expression makes normally tumor-resistant mice more prone to tumor development.