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A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

LncRNA MSTRG.14227.1 hinders hair follicle development in cashmere goats, affecting cashmere quality.

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

Targeting METTL1 may help slow papillary thyroid cancer growth and spread.

The LMNA mutation affects skin structure even in asymptomatic carriers.

HPV8 causes hair follicle stem cells to grow, leading to skin lesions.

A new protein linked to hair strength was identified, aiding in understanding brittle hair conditions.

COVID-19 may harm male fertility by affecting sperm production.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

Misbehaving hair follicle stem cells can cause hair loss and offer new treatment options.

The gene HDC is important for the development of hair follicles in newborn mice.

Keratin 18 helps diagnose and predict cancer progression and affects cancer growth and spread.

The technology can help diagnose and subtype autoimmune diseases by identifying specific autoantibodies.

LncRNA018392 helps goat skin cells grow by increasing CSF1R.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

Hair follicle stem cells reduced hair loss and inflammation in mice with a condition similar to human alopecia.

Aromatase gene variation may increase female hair loss risk.

Overexpressing Merkel cell virus proteins in human hair follicles can create clusters of cells that resemble Merkel cell cancer.

A woman with a long-term skin condition developed a serious skin cancer that led to her death.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

AP-1 and TGFß work together to drive resistance in basal cell carcinoma, suggesting new treatment options.

Gene therapy has potential as a future treatment for Hutchinson-Gilford progeria syndrome.

Mutations in the hairless gene cause a rare form of permanent hair loss.

miR-214-3p helps nerve repair and recovery.

The study provides exploratory findings on miRNA changes in female hair loss.

CTHRC1 helps sweat glands recover by rebuilding nearby blood vessels.

A gene mutation causes a rare hereditary hair loss, offering potential for new treatments.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

Sex steroids affect the MafB gene differently in male and female hamsters.