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The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

Oregano extract helps fix testis and sperm damage caused by finasteride.

Blocking the ATX-LPA pathway may improve insulin sensitivity and mitochondrial function in obesity.

Smoking reduces antioxidants and causes DNA damage in hair follicles.

Using A132 hair dye with sunlight can cause skin damage and hair loss.

EDA2R gene linked to hair loss.

Healthy mitochondria in skin cells are essential for proper hair growth and skin cell interaction in mice.

Taking riboflavin and eating less lysine can help some people with a specific genetic disorder avoid brain damage.

Improving mitochondrial health may better treat atherosclerosis than antioxidants.

Skin cells from people with Epidermolysis Bullosa Simplex have abnormally placed and less active mitochondria.

The congress highlighted new gene therapy techniques and cell transplantation methods for treating diseases.

MFN2 mutations cause mitochondrial problems, leading to more upper body fat and lower leptin levels.

Researchers created a model to understand heart aging, highlighting key genes and pathways, and suggesting miR-208a as a potential heart attack biomarker.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

MFN2 mutations cause mitochondrial problems, unusual fat distribution, and low leptin despite high body fat.

Minoxidil may protect the brain from damage by preventing cell death and energy loss.

Two rare genetic diseases cause severe rickets in children due to defects in vitamin D metabolism.

K_ATP channel gene mutations are linked to heart diseases, but more research is needed to understand the connection and treatment potential.

Involucrin gene expression is controlled by specific proteins and signaling pathways.

Men generally have more severe COVID-19 cases and higher death rates than women due to biological differences.

Human mitochondrial DNA polymerase makes very few errors, crucial for preventing degenerative diseases.

Certain genes control the color of human hair by affecting pigment production.

Mice without the vitamin D receptor gene lose hair due to disrupted hair follicle cycles.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

The document concludes that understanding genetic mutations in the PI3K-AKT-mTOR pathway can lead to better diagnosis and treatment for certain genetic skin disorders.

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

Chinese domestic goats have unique genetic traits due to domestication and geographic isolation.

Genetic variations greatly affect individual metabolism and can impact health and disease risk.

Ancient Chinese goats evolved cashmere-producing traits due to selective breeding, particularly in genes affecting hair growth.

Women generally handle heart enlargement better than men, but it's riskier for them if it occurs; hormones like estrogen offer some protection.