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Mutations in the LSS gene cause hair loss and may affect brain development, with varying severity.

Keratinocytes can reduce the survival of certain melanoma cells, suggesting new therapy paths.

Nucleophilic reagents break down hair keratin, forming more lanthionine and lysinoalanine than in wool.

Ceramide synthase 4 is essential for maintaining skin barrier health.

GLI2 increases follistatin production in human skin cells.

The research found that Atypical Progeroid Syndrome has unique symptoms and is not caused by the buildup of a certain mutant protein.

A Gsdma3 mutation causes hair loss due to stem cell damage from skin inflammation.

The new model helps understand and develop treatments for genetic skin disorders like AEC.

A new mouse mutation causes skin and hair defects due to a gene change.

Hair growth is controlled by specific gene clusters and proteins, and cysteine affects hair gene expression in sheep.

Biotin mega-dose therapy led to dramatic improvement in a newborn with a rare metabolic disorder.

A wide range of proteins are integrated into the skin's protective layer.

The Ysc84/SH3yl1 protein family is important for cell movement and the process of taking in materials by interacting with actin and cell membranes.

Very-long-chain acyl-CoA synthetases and fatty acid transport proteins play key roles in fatty acid metabolism and lipid processing in different tissues.

PROTACs offer new ways to treat hard-to-target diseases, with promising drugs for cancer in advanced trials.

The ZIP7 gene helps control zinc levels in cells by moving zinc from the Golgi apparatus to the cytoplasm.

A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

The muscle damage was caused by T-cell large granular lymphocytic leukemia, not dermatomyositis.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

Lack of functional CYLD in mice leads to early aging and cancer.

Reconstructed skin models are useful for studying how skin processes certain chemicals.

Abnormal amino acid metabolism may worsen rosacea symptoms.

GLI2 activates GLI1, promoting skin tumor growth and hair development.

Ca²⁺-mediated protein citrullination controls cell growth in the CNS and may help treat brain tumors.

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

Introducing the rat OTC gene partially corrected OTC deficiency in mice.

NGAL may help maintain skin balance and is linked to skin disorders and cancers.

CD8+ T cells attack hair follicle stem cells, causing scarring and hair loss.

A genetic variant in the GJB6 gene likely caused the Labrador's paw pad condition.