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Colorectal cancer cells can adapt without losing their traits or drug sensitivity.

The technique effectively shows how human skin and hair cells form into ball-like structures.

Blocking TSLP reduces skin inflammation and cell overgrowth in psoriasis.

CYLD mutations cause a variety of skin tumors with symptoms starting around age 16, and treatments are currently limited.

Most people with systemic lupus erythematosus have skin problems, and skin symptoms are often the first sign of the disease.

Aging in one type of stem cell can cause aging-like changes in various organs.

Tislelizumab can cause cutaneous lupus erythematosus.

A woman's long-term scalp issues were diagnosed as a rare skin disorder called cutaneous Langerhans cell histiocytosis.

Radiological findings help distinguish LAM, PLCH, and BHD to avoid invasive tests.

A new mutation in the STS gene causes X-linked ichthyosis, even in rare female cases.

Clascoterone safely promotes hair growth similar to minoxidil.

A child with skin and heart issues had rare genetic mutations affecting skin and heart cell cohesion.

Dietary L-serine supplementation can reduce symptoms of HSAN1 by lowering harmful 1-deoxySL levels.

Mice with too much Claudin-6 have skin barrier problems and abnormal hair growth.

SLE patients experience hair loss similar to telogen effluvium, with hair damage and immune activity at hair follicles.

The patient's scalp lesions stabilized with a combination of treatments after initial therapies failed.

A 31-year-old woman was diagnosed with Complete Androgen Insensitivity Syndrome much later than usual, leading to a call for earlier detection and treatment guidelines.

Early diagnosis and coordinated care are crucial for managing lupus effectively.

PCOS care in Singapore can be bettered by refining referral systems, standardizing diagnosis and treatment, enhancing complication screening, and offering educational resources for clinicians.

A child has a rare hair and skin disorder due to specific gene variants, suggesting broader genetic testing is needed.

A new, quick method was developed to analyze skin lipids, discovering a new ceramide subclass.

HTLV-1-associated lichenoid dermatitis (HALD) is linked to an immune response against HTLV-1-infected cells.

Blocking the NOTCH pathway can prevent fibrosis in systemic sclerosis.

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

The number of new cases of cutaneous B-cell lymphoma has leveled off since the early 2000s, and survival rates have improved since 1973.

CCCA may involve the PD1/PDL1 pathway and increased caspase 3, leading to permanent hair loss.

Two sisters with lipoedematous scalp suggest a genetic influence in the condition.

Soy hull supplement does not affect sheep and lamb growth or reproductive performance compared to corn-based supplements.

Two siblings were the first reported cases of inheriting both eye coloboma and loose anagen syndrome together.