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ZmSPL10, ZmSPL14, and ZmSPL26 genes are essential for forming maize structures needed for pollen capture and kernel production.

CYP154C7 enzyme can effectively modify steroids and is promising for commercial use.

Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.

Complex basal cell carcinomas need personalized treatment due to unique genetic mutations.

The CRABP I gene in cashmere goats is highly conserved but has unique features at specific amino sites.

Increasing PBX1 reduces aging and cell death in hair follicle stem cells by boosting SIRT1 and lowering PARP1 activity.

Targeting protein S-palmitoylation could lead to new skin disease treatments.

A child with skin and tooth symptoms was found to have a genetic mutation causing cardiocutaneous syndrome, leading to heart problems.

Sebaceous gland atrophy and abnormal function may contribute to hair loss in psoriasis.

Protein kinase C epsilon may promote skin cancer development after UV exposure by affecting nearby cells.

The Hippo signaling pathway helps control organ size during regeneration by regulating gene expression.

The study identified a key protein involved in producing underarm odor and found ways to inhibit it.

SPT6 prevents excessive skin inflammation by blocking a feedback loop.

Certain mutations in the PADI3 gene may increase the risk of developing a type of scarring hair loss common in women of African descent.

Tanning ability is linked to specific DNA changes in skin genes.

White lupin uses specific genes to grow root hairs and access phosphorus when it's scarce.

Blocking TSLP reduces skin inflammation and cell overgrowth in psoriasis.

Removing SIX1 in fat cells reduces skin fibrosis.

A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

Shorter CAG repeats in a specific gene may increase male hormone activity and symptoms like acne and excess hair in women with PCOS.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

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

SASH1 gene mutations are linked to various inherited skin pigmentation disorders.

Protein kinase C epsilon may increase skin cancer risk by affecting nearby cells.

Astrotactin2 affects hair follicle orientation and skin cell polarity.

PrrH sRNA controls pyochelin gene expression in Pseudomonas aeruginosa based on heme levels.

CRISPR/Cas9 editing in spinach affects root hair growth by altering specific genes.

Plakophilin 1 helps control skin cell immune responses to prevent excessive inflammation.