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Hair follicle hyperplasia is common in both benign and malignant skin lymphoproliferative disorders, with a proposed new term "pseudolymphomatous adnexitis."

The LEF-1 binding site enhances gene expression in hair follicles, with other proteins aiding specific regulation.

Low-dose chemotherapy is safer, more effective, and cost-effective than surgery for treating bone lesions in children.

The tumor suppressor gene FLCN affects mitochondrial function and energy use in cells.

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

A woman with chronic hepatitis C had a rare skin condition linked to her illness.

A new mutation linked to partial Androgen Insensitivity Syndrome and prostate cancer was found in a patient unhappy with their female gender assignment.

Two rare bald spots on the back of the scalp were found to be lupus, not alopecia areata.

Anti-phospholipid antibodies in SLE can cause thrombosis and bone necrosis.

Higher TGF-β signaling may increase skin cancer risk in organ transplant recipients.

The article concludes that hair loss is a common side effect of drugs treating skin cancer by blocking the hedgehog pathway, but treatment should continue, and more selective drugs might prevent this side effect.

Thymic LCH may be underdiagnosed, so thymic ultrasound should be considered in infants with cutaneous LCH.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

A new TP63 mutation was found in a baby with EEC syndrome, showing the need for TREC testing to check for immune issues.

Proteolytic enzymes damage hair follicles by detaching stem cells.

A rare autoimmune disease caused the woman's scalp blisters and hair loss, successfully treated with medication.

Hair loss in Lichen Planopilaris is caused by immune system issues damaging hair follicles and stem cells.

The research shows that skin cancer likely originates from hair follicles and that certain cell populations expand to promote skin cancer growth.

Non-coding RNAs may be key in diagnosing and treating rare skin disorders.

Increasing SSAT makes skin more prone to cancer.

New gene mutations linked to skin conditions were found, bacteria and chemicals may worsen acne, a dog mutation could exist in humans, virus-like elements might be involved in psoriasis, and a vitamin D3 treatment doesn't prevent chemotherapy-related hair loss.

Genetic variations affecting skin structure play a key role in severe acne.

Baricitinib effectively treated hair loss and inflammation in a patient with alopecia areata and lichen planopilaris.

Basal cell carcinomas may use IDO to protect themselves from the immune system.

Lupus can affect the scalp and nails, often causing hair loss and nail damage, and needs early aggressive treatment to prevent permanent damage.

CCCA and lichen planopilaris have similar histological features, making them hard to distinguish.

The Brigham Eyelash Tool for Alopecia (BELA) is a reliable way to measure eyelash loss in alopecia areata patients.

A woman with lupus and antiphospholipid syndrome had bone damage, showing the need for careful treatment.