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A boy with a rare skin condition and kidney disease improved with cyclosporine after steroids failed, suggesting a new treatment approach.

XEDAR deficiency prevents muscle degeneration in EDA-A2 transgenic mice.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

Stress activates a special function of the Vitamin D receptor with the help of c-Jun, which can also prevent cell death.

Hair cortisol measurement can help diagnose and monitor Cushing’s disease.

Over half of the dog skin disorders discussed have known gene variants, enabling genetic testing for diagnosis and responsible breeding.

The Hedgehog signaling pathway is linked to cancer development, and targeting it with inhibitors shows promise but faces challenges like resistance.

Clouston's syndrome is a rare disorder affecting nails, hair, teeth, and skin, caused by a gene mutation, and currently has no treatment, only supportive care.

The research identified six functional hair keratin genes and four pseudogenes, providing insights into hair formation and gene organization.

Researchers found a safe and effective way to pick genetically modified skin cells with high growth potential using CD24.

lncRNAs play a key role in hair follicle development, affecting cashmere quality and yield.

Comprehensive genetic testing and international collaboration are crucial for better understanding and managing Ehlers-Danlos syndromes.

Hair loss in Cronkhite-Canada syndrome may be due to an autoimmune response.

Genetically modified sheep with more β-catenin grew more wool without changing the wool's length or thickness.

CFx-δ2 from stem cells helps heal burn wounds faster.

AcD scaffolds improve tissue repair and regeneration by combining stem cells with a supportive matrix.

A new gene variant causes glucocorticoid resistance in a mother and son.

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.

Two new gene mutations cause a rare hair disorder.

Altering SSAT affects fat metabolism and body fat in mice.

Removing SIX1 in fat cells reduces skin fibrosis.

The research suggests that SFRP2 and PTGDS proteins might be indicators of female pattern hair loss and could contribute to hair loss.

Mutating the gmds gene in zebrafish increases hair cell numbers and regeneration.

Two new gene clusters important for hair formation were found on human chromosome 11.

Removing integrin α3β1 from hair stem cells lowers skin tumor growth by affecting CCN2 protein levels.

Sry may regulate fatty acid metabolism and shows different expression levels in rat tissues.

MEF2C is crucial for normal hair cycle progression.

Certain gene variations may increase the risk of PCOS in South Indian women.

Prednisone treatment helped a woman with Cronkhite-Canada syndrome recover from hair loss and digestive issues.