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Including special area involvement helps identify more psoriasis patients who may need systemic treatment.

Reduced TRPS1 leads to increased STAT3 and SOX9 in hair follicles, affecting hair growth.

LGR5 and LGR6 are expressed differently in various skin tumors, which may offer clues about their origins.

A specific DNA pattern in Malassezia restricta may be linked to hair loss in men.

Somatic BHD mutations are rare in Japanese renal tumors.

Researchers found four distinct fibroblast types in human skin, which could help in treating wounds and fibrotic diseases.

Researchers mapped and categorized specific keratin-associated protein genes on human chromosome 21q22.1.

A new ARID1B gene variation causes Coffin-Siris syndrome 1 and early high myopia in a Chinese family.

Two genetic variations in Moa buffalo help them adapt to heat.

A new type of nerve cell involved in itch perception was discovered.

Genetic analysis is crucial for diagnosing and managing cerebral arteriopathy.

Blocking Hedgehog signaling offers new treatment options for advanced basal cell carcinoma.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

The research found how GPCR Class A Rhodopsin receptors are related and suggested possible substances they interact with.

Basonuclin is crucial for hair follicle development and cycling in mice.

Certain gene variations may increase the risk and severity of alopecia areata.

Different PADI isoforms help cells develop diverse functions.

The study identified key immune cell differences between mild and severe alopecia areata.

PTCH gene mutations contribute to basal cell carcinoma development.

A genetic mutation in the hHa1 gene creates a smaller, but still functional, hair protein without causing hair problems.

Some prostate cancers have gene changes that may affect treatment with certain drugs.

A new IL6ST gene variant may cause a unique form of hyper-IgE syndrome with skin abscesses and high IgE levels.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

ANE syndrome is caused by a mutation in the RBM28 protein that disrupts ribosome assembly.

BIVV009 is a safe treatment for bullous pemphigoid that reduces C3 deposition without harmful side effects.

Corticosteroids can reduce scarring in acne keloidalis by targeting specific cells.

The RAS pathway affects hair growth differently in CFCS and CS.

Genetic changes in specific proteins contribute to hair loss in some women of African descent.

Basonuclin helps keratinocytes multiply and prevents them from fully maturing.