Search

everythinglearnresearchcommunity

for

Search:↓

Older age, pre-existing skin conditions, cirrhosis, and pegylated interferon use increase the risk of skin issues during hepatitis C treatment.

A complex X chromosome rearrangement can increase the risk of multiple autoimmune diseases.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

Ptch2 plays a key role in controlling stem cell function and the ability to regenerate after birth.

The study found two new mutations in a Chinese patient with severe biotinidase deficiency.

Autophagy helps control skin inflammation and cancer responses and regulates hair growth by affecting stem cell activity.

Male and female hair loss have different genetic causes.

Certain fats in the blood are linked to an increased risk of male pattern baldness.

Genes and epigenetic changes are important in the development of Polycystic Ovary Syndrome.

Six genetic conditions are often linked to complete scalp hair loss in children.

Environmental factors and chemicals might affect hormone balance and contribute to common hair loss.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

Genetic factors play a major role in acne.

American men are older, more obese, and have longer infertility than Canadian men.

Hair follicle-derived IL-7 and IL-15 are crucial for maintaining skin-resident memory T cells and could be targeted for treating skin diseases and lymphoma.

Common variants in the Trichohyalin gene are linked to straight hair in Europeans.

Patched1 helps prevent tumors by controlling cell growth.

The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

Scientists successfully created mouse hair proteins in the lab, which are stable and similar to natural hair.

Different signals work together to change gene activity and guide hair follicle stem cells to become specific cell types.

Scientists found a specific group of itch-sensing nerve cells in mice important for feeling itch but not for sensing heat or touch.

GALT5 and GALT2 are important for plant growth and development because they help with protein glycosylation.

Notch signaling is essential for healthy skin and hair follicle maintenance.

Certain mouse strains develop a skin condition similar to a human hair loss disease due to genetic defects.

Loss of OGG1 increases skin inflammation and auto-antibodies in lupus.

Significant progress was made in understanding PXE, but effective treatments are still needed.

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

Testosterone replacement is recommended for men with low testosterone levels and symptoms of hypogonadism.

SIRT7 protein is crucial for starting hair growth in mice.

A mutation in the IKZF1 gene causes immune system overactivity, linked to autoimmune diseases like lupus.