Search

everythinglearnresearchcommunity

for

Search:↓

Sons of mothers with polycystic ovary syndrome (PCOS) have a higher risk of obesity and insulin resistance, possibly due to certain genes and factors passed down from their mothers.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

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

A man's unusual scalp folds caused by a skin condition were treated with surgery and remained unchanged two years later.

Two new gene mutations cause a rare hair disorder.

Understanding genetics is crucial for treating heart and skin diseases.

Advanced nanocarrier and microneedle drug delivery methods are more effective, safer, and less invasive for treating skin diseases.

Acne inversa is an epithelial-driven disease where inflammation is caused by cyst rupture, and treatments should focus on preventing tendril growth for better results.

VHL disease can cause early paragangliomas, needing lifelong monitoring.

The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

A new mutation in the mitochondrial DNA was found in a boy with MELAS, even though his family didn't show typical signs.

A gene mutation in mice causes severe skin disorder similar to a human condition.

Some people with schwannomatosis have a new type of mutation in the LZTR1 gene.

A boy with Pachyonychia congenita has a confirmed gene mutation, highlighting the need for a local genetic database in India.

Revertant cell therapy could be a future treatment for Ichthyosis with confetti.

PAON shows skin patterns due to genetic mosaicism.

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

Polyomavirus A2 infection in newborn mice caused hair follicle tumors.

Scientists found gene mutations that affect hair loss, skin stem cells, and skin disorders, and identified drugs that may help treat blood vessel and skin conditions.

Skin cancer often starts from Lgr5+ progenitor cells.

The junction of the inner and outer prepuce with good blood flow is ideal for surgical flaps.

Certain genetic markers on the Y-chromosome may influence prostate cancer risk in Iraqi males.

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.

The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.

A patient with a scalp condition and benign skin tumor experienced hair loss and did not improve with treatment, choosing not to have surgery despite a small cancer risk.

A rare skin disorder, nevus comedonicus, can appear on one side of the body following Blaschko's lines.

A rare skin infection in a 10-year-old kidney transplant patient was successfully managed by adjusting medication.

Antiviral medication valganciclovir may improve skin and hair in Trichodysplasia Spinulosa patients.

A young girl's foot lesion was actually a rare condition caused by a hair fragment under the skin, not a parasite.