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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.

A new type of hereditary hair loss in a Chinese family is linked to chromosome 2p25.1–2p23.2.

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

A man developed male breast cancer after four years of finasteride treatment for an enlarged prostate.

Connexin-26 gene mutations may increase cancer risk in KID syndrome patients.

A new DSG4 gene mutation causes hair defects in a young girl.

A genetic defect in an Appenzeller Mountain Dog caused skin issues, improved with ketoconazole, showing the importance of advanced genetic testing.

A rare case of trichothiodystrophy was found with autism, seizures, and mental retardation.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

External factors can cause skin cancer cells that usually don't spread to grow and form tumors in mice.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Boron neutron capture therapy for head and neck cancer can cause side effects like mouth sores and skin irritation, which vary depending on where the treatment is aimed.

The hr gene is linked to hair loss in Valle del Belice sheep.

ATP-dependent chromatin remodeling is crucial for skin development and stem cell function.

A new mutation, Glu402Lys, in hair keratin is linked to variable symptoms of monilethrix.

Genetic testing confirmed a rare disorder causing hair loss and vision problems in a Saudi family, stressing its importance for diagnosis and counseling.

Melanoma risk tools need improvement, certain gene mutations cause skin diseases and could be treated by targeting those mutations, skin wrinkling may relate to lung aging due to genetic factors, and oxidative stress affects hair loss but can be reduced in low oxygen.

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

Rapamycin reduces skin cell growth and tumor development by affecting cell signaling in mice.

5% topical minoxidil improves hair density and quality in monilethrix patients.

An 8-year-old boy with Recklinghausen's Disease shows various symptoms and is from a family with close genetic ties.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

Genetic factors might cause fibrosing alopecia linked to hair shaft abnormalities.

Bald areas have lower cell growth, more DNA damage, and increased cell death.

A standardized scoring system is needed to improve model reliability for predicting hair loss in brain tumor patients treated with proton therapy.

A mutation in the KRT74 gene causes tightly curled hair.

A boy with a new NR5A1 gene mutation has a sex development disorder without affecting his adrenal glands.

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