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Sunlight simulation causes skin inflammation, with different skin types reacting at different levels of exposure.

Researchers developed a cost-effective 66 K SNP chip for cashmere goats that is accurate and useful for genetic studies.

Longer TA repeats in the SRD5A2 gene may increase acne risk in Chinese people.

RCS-01 is safe and may help rejuvenate aging skin.

Genetic variations contribute to over 10% of recurrent early pregnancy loss cases.

Scientists developed a new way to study mutations in a skin condition using blood cells, which may help diagnose and treat the disease.

SIRT7 protein is crucial for starting hair growth in mice.

PRX102 is essential for rice root hair growth by helping transport substances to the tips.

The DMI3 gene is essential for nodule development and symbiosis in certain plants.

CT-707 is effective and safe for treating certain Chinese lung cancer patients.

The 675 nm laser effectively improved facial acne scars in dark skin with minimal side effects.

Seven genetic variations in sheep's DSG4 gene are linked and affect wool traits.

A new gene mutation causes insulin resistance in a girl and her mother.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

Tissue-engineered skin substitutes can model junctional epidermolysis bullosa and may help develop gene therapy.

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

Non-coding RNA boosts retinoic acid production and signaling, aiding regeneration.

RD26 controls root hair growth during drought by repressing key genes, helping plants save energy.

Sheep breeds show different keratin gene expression in the groin, linked to hair follicle density.

LDE225 is a promising skin-applied treatment for basal cell carcinoma with good skin penetration and effectiveness.

The research showed that CRISPR/Cas9 can fix mutations causing a skin disease in stem cells, which then improved skin grafts in mice, but more work on safety and efficiency is needed.

The prototype for analyzing skin aging works technically and clinically.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

TRα and CRABPII genes change their activity levels during goat fetal skin development.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.

Human hair keratin genes have unique simple sequence repeats that may help track genetic variations.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.