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A man with Acrodermatitis continua did not get better with etanercept treatment, and his condition worsened, suggesting treatment effectiveness may vary by genetics and race.

A protein from fat-derived stem cells, DKK1, is linked to hair loss and blocking it may help treat alopecia areata.

Genetic factors play a major role in acne.

The PP2A-B55α protein is essential for brain and skin development in embryos.

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

Dermatoscopy can help diagnose CCCA without visible hair loss, offering a less invasive option than biopsy.

CPK1 helps root hair growth in Arabidopsis by activating channels for calcium signaling.

Men with CCCA often face delayed diagnosis and severe hair loss, highlighting the need for earlier recognition and treatment.

Certain genes help dermal papillae cells in hair follicles grow and group together.

Researchers found a white halo around hair in most patients with a specific type of hair loss, which helps in early diagnosis and treatment.

CAH is a genetic disorder affecting cortisol production and causing hormonal imbalances, with treatment and diagnosis varying by form and symptoms.

Phospholipase Cδ1 is crucial for normal skin and hair development.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

New digital tools are improving the diagnosis and understanding of irreversible hair loss conditions.

A new classification for trichothiodystrophy helps identify genetic causes and potential treatments.

A specific mutation in PA-PLA1α causes abnormal hair growth.

Removing MCPIP1 from myeloid cells in mice leads to hair loss and prevents skin tumors but causes pigmented spots.

High CRP levels could indicate vitamin D deficiency in people with alopecia areata.

Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.

Diphencyprone increases Bcl-2 protein in patients with hair regrowth from alopecia areata.

Fibrosing alopecia in a pattern distribution is a unique hair loss condition with inflammation and scarring, resembling but distinct from common balding.

P-cadherin is important for hair growth and health, and its problems can cause hair and skin disorders.

The clinical signs of Adams-Oliver syndrome can vary greatly, even among family members.

The CTLA-4 gene polymorphism does not affect polycystic ovarian syndrome.

The PCR technique can identify genetic differences in a wool-related gene among different sheep breeds, which may help improve wool and pelt quality.

A new test helps find drugs to treat head and neck cancer by targeting c-Rel.

PICAT is a reliable tool for assessing dermatology residents' skills in PRP procedures for hair loss.

ILC1-like cells can cause alopecia areata by themselves.

A new genetic mutation was found causing hair and eye issues in a boy.

A specific gene mutation causes a severe skin disorder in a family.