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Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Blocking 11β-HSD1 can lessen the harmful effects of glucocorticoids on hair growth cells.

MARCKSL1 is important for wound healing and could be a target to reduce scarring.

The enzyme is crucial for skin cell development and can be activated without proteolytic activation.

Increasing SSAT makes skin more prone to cancer.

A peptide known for reducing wrinkles also effectively inhibits an enzyme linked to skin inflammation and acne.

Researchers found specific genes in the part of hair follicles that could help treat hair disorders.

The ID2 gene can help distinguish between sensitizers and irritants in skin cells.

Deleting the CDSN gene causes severe skin and hair problems, leading to death.

Vesiculobullous lesions should be considered part of canine cutaneous epitheliotropic T-cell lymphoma.

Cells that move well may improve hair loss treatments by entering hair follicles.

The specific skin disease variant p.(Arg2000Trp) in plectin can cause a wide range of symptoms, which should be considered when diagnosing patients.

A heart transplant patient developed a skin condition called epidermodysplasia verruciformis after taking immune-suppressing drugs.

Squaric acid dibutylester can cause severe skin reactions in people with allergies.

A peptide called DPS-1 helps human scalp cells grow and stimulates hair growth in mice.

Patients with Shwachman-Diamond syndrome often get misdiagnosed due to a wide range of symptoms, including immune system problems and bone abnormalities.

Plakophilin 1 helps control skin cell immune responses to prevent excessive inflammation.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.

Overexpressing NSD3 in mice causes breast cancer-like tumors and gland abnormalities.

A new genetic disorder caused by an ODC1 mutation can be treated with DFMO.

NSC167409 can effectively inhibit the virus causing hand, foot, and mouth disease.

XEDAR deficiency prevents muscle degeneration in EDA-A2 transgenic mice.

Delta1 is crucial for controlling skin cell growth and preventing tumors in mice.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

CD19-CAR T cell therapy may help regenerate skin in systemic sclerosis.

Blocking certain pathways with kinase inhibitors may help treat cutaneous lupus erythematosus.

Higher levels of PD-L1 are linked to more severe hair loss in people with Alopecia Areata.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

SASH1 gene mutations are linked to various inherited skin pigmentation disorders.

A Gsdma3 mutation causes hair loss due to stem cell damage from skin inflammation.