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A mutation in the SREBF1 gene causes both hereditary mucoepithelial dysplasia and IFAP syndrome, which are related conditions.

LSD1 is crucial for regenerating hair cells in zebrafish.

Sulfated polysaccharides from Microcosmus exasperatus may help treat cancer without causing blood thinning.

Sphingosine 1-phosphate helps control mechanical pain.

The study suggests that higher levels of SIRT1 and SIRT2 may improve overall cell health and aging processes.

High levels of ODC and a mutant Ha-ras gene cause tumors in mice.

Asiaticoside can improve wound healing after ESD by promoting tissue repair and reducing inflammation.

The search scheme SMRI is faster and more secure for retrieving encrypted data from the cloud.

A 4kb fragment of the desmocollin 3 promoter targets gene expression to specific skin and hair follicle areas.

LHX2 is crucial for development, tissue repair, and preventing diseases.

Certain genetic markers can indicate higher or lower risk for systemic lupus erythematosus.

Scientists found new, better-working inhibitors for a hormone-related enzyme.

Sargassum horneri extract speeds up burn healing and reduces inflammation.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

Tissue-engineered skin substitutes can model junctional epidermolysis bullosa and may help develop gene therapy.

Adipose stem cells show common protein changes as they grow, especially involving S100A6.

Aerobic exercise helps protect the intestines by improving their barrier function.

ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.

Lack of Cisd2 disrupts calcium balance in cells, leading to poorly functioning neutrophils.

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

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

Sox9 levels in brain stem cells affect whether they stay as stem cells or become neurons.

Two new proteins, hKAP1.6 and hKAP1.7, are found in the hair follicle cortex.

One twin girl has Loose anagen syndrome with poorly anchored hair, diagnosed with a simple hair pull test, while her identical twin does not have the condition.

The hydrogel works quickly to stop bleeding and prevent infection, making it a promising first-aid bandage.

SP1 promotes and KROX20 inhibits hair cell growth by affecting the CUX1 gene.

Sheep cells were successfully modified to include a spider silk protein gene.

Mutations in the KLHL24 gene cause a skin disorder in some Russian families.

Targeting ACE2 and TMPRSS2 may help prevent or treat COVID-19 in cancer patients.