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The study found that a specific genetic variation in the TNFα gene is significantly linked to Alopecia Areata in the Jordanian Arab population.

The genes KRT25 and SP6 affect curly hair in horses, with KRT25 also causing hair loss. If both genes are mutated, the horse gets curly hair and hair loss. KRT25 can hide the effect of SP6.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.

Certain genetic variants linked to immune response increase the risk of alopecia areata in Taiwanese people.

Runx1 controls fat-related genes important for normal and cancer cell growth, affecting skin and hair cell behavior.

Women with nonclassic 21-hydroxylase deficiency can have successful pregnancies through IVF, with certain factors affecting their chances.

No link found between new male baldness genes and female hair loss.

Ichthyosis with confetti is a genetic skin disorder with consistent ectodermal malformations and various KRT10 gene mutations.

Cantú syndrome may be linked to pituitary adenomas.

Researchers created a mouse model for Cushing's syndrome to study glucocorticoid excess and potential treatments.

Poor maternal nutrition can lead to fewer wool follicles in Chinese Merino sheep.

Skin lesions in Carney Complex are caused by a gene change in some skin cells that leads to increased pigmentation and may lead to tumors.

Mirex seems to promote a unique group of skin cells different from those affected by another tumor promoter, TPA.

Genetic data can predict male-pattern baldness with moderate accuracy, especially for early-onset cases in some European men.

Cavity macrophages gather on organ surfaces but don't really invade or help repair the organs after injury.

The research found that PCOS has common genetic factors regardless of how it is diagnosed and is linked to metabolic and reproductive issues.

Certain gene variations are linked to higher male hormone levels in Chinese women with PCOS and insulin resistance.

A specific genetic deletion in goats affects cashmere yield and thickness.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

Standardized procedures are crucial for collecting and preparing biological samples to ensure accurate clinical metabolomics results.

mTOR signaling helps activate hair stem cells by balancing out the suppression caused by BMP during hair growth.

PTEN helps control the number and health of skin stem cells by working with the protein BMAL1.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

The Sonic hedgehog pathway is crucial for new hair growth during mouse skin healing.

Stem cells help remove dead cells to keep tissues healthy by balancing cell replacement and clearance.

A gene called HDAC9 might be a new factor in male-pattern baldness.

No single biomarker is reliable enough for diagnosing and assessing SLE.

β-catenin in the dermal papilla is crucial for normal hair growth and repair.

Oxidative stress plays a significant role in alopecia areata, and new treatments may include JAK inhibitors and antioxidants.