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New liposome treatment successfully delivers CRISPR to deactivate a key enzyme in androgen-related disorders.

The UD-PrOZA program successfully diagnosed 18% of adult patients with rare diseases, often using genetic testing.

Certain natural and synthetic compounds may help treat inflammatory skin diseases by targeting a specific signaling pathway.

Mutations in the androgen receptor gene cause different levels of androgen insensitivity, making it hard to create simple tests for the condition.

A gene in Sebekia benihana, CYP-sb21, is needed for a specific reaction on the drug Cyclosporine A, which could be important for hair growth without affecting the immune system.

Early hair loss may indicate prostate issues.

Diabetes can lead to blindness and skin problems, and managing blood sugar and blood pressure is crucial to prevent these complications.

Wnt1/βcatenin signaling is crucial for heart repair after injury.

Researchers identified genes linked to coat color, body size, cashmere production, and high altitude adaptation in goats.

Damaging mitochondrial DNA in mice speeds up aging due to increased reactive oxygen species, not through the p53/p21 pathway.

Estrogen increases blood vessel growth factor production, while testosterone blocks this increase.

Dynamic, light touch is sensed through a common mechanism involving Piezo2 channels in sensory axons.

Targeting NETs may help reduce fibrosis in Crohn's disease.

Mice without the vitamin D receptor have bone issues and other health problems, suggesting vitamin D is important for preventing various diseases in humans.

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

The timing of when the gene Bmal1 is active affects aging and survival, with its absence during development, not adulthood, leading to premature aging.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

Skin bacteria, specifically Staphylococcus aureus, help in wound healing and hair growth by using IL-1β signaling. Using antibiotics on skin wounds can slow down this natural healing process.

Non-coding RNAs play key roles in the hair growth cycle of Angora rabbits.

The document concludes that anti-dsDNA antibodies are not unique to SLE and their use as indicators is doubtful, highlighting the need for better understanding and classification of the disease.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

Treg dysfunction is linked to various autoimmune skin diseases, and understanding Treg properties is key for new treatments.

A specific protein in chicken embryos links early skin layers to feather development.

Bleaching hair damages protein structure, especially keratin, leading to weakened hair.

Telomere damage affects skin and hair follicle stem cells by messing up important growth signals.

Vitamin D boosts a specific gene activity in kidney cells that could improve heart and kidney function.

Key genes linked to hair growth and cancer were identified in hairless mice.

STAT3 signaling is important for healthy skin and hair follicles, and its disruption can lead to skin conditions like atopic dermatitis.