Search

everythinglearnresearchcommunity

for

Search:↓

The Asiatic lion has very low genetic diversity and unique genetic traits, highlighting the need for its conservation.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

The study found no significant link between Helicobacter pylori infection and polycystic ovary syndrome in young females.

A specific hair protein variant increases the spread of breast cancer and is linked to worse survival rates.

The research identified 12 antioxidant compounds in Polygonum multiflorum roots, suggesting these as quality markers for the plant's processed roots.

PAD3 plays a key role in hair and skin protein structure and may be linked to skin diseases.

Iron deficiency in menstruating women causes many health issues beyond anemia and needs early detection and treatment.

EGFR helps control how hair grows and forms without needing p53 protein.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

Acne treatment with isotretinoin increases the presence of p53, a protein, in skin and oil glands, which may help reduce acne severity.

Proteins like aPKC and PDGF-AA, substances like adenosine and ATP, and adipose-derived stem cells all play important roles in hair growth and health, and could potentially be used to treat hair loss and skin conditions.

Removing part of the vitamin D receptor stops vitamin D from working properly.

Blocking BACE1 and BACE2 enzymes causes hair color loss in mice.

Microneedle arrays with nanotechnology show promise for painless drug delivery through the skin but need more research on safety and effectiveness.

Girls with PCOS during adolescence have a higher risk of developing type 2 diabetes, and early treatment can help manage this risk.

Polygonum multiflorum extract helps hair grow longer and fights the effects of hormones that cause hair loss.

Wnt proteins from certain skin cells are crucial for normal hair growth and renewal.

Finasteride affects young male rats' brain function and behavior negatively.

A new drug delivery system using oil body-bound oleosin-rhFGF-10 improves wound healing and hair growth in mice.

A compound from brown algae boosts the production of a certain inflammatory substance in skin cells.

Removing the ROBO4 gene in mice reduces skin inflammation and hair loss by affecting certain inflammation pathways and gene expression.

Anabolic steroids boost muscle growth, SARMs increase muscle mass and bone density without side effects, and myostatin inhibitors block a protein that stops muscle growth, but each has potential risks.

Women with non-classic congenital adrenal hyperplasia have higher risk for heart and metabolic problems.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Glycogen metabolism is important for energy and processes in human hair follicles, and hair follicles may produce glucose from lactate.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

SHBG may be a useful early indicator and treatment target for PCOS.

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

Foxi3 expression in developing teeth and hair is controlled by the ectodysplasin pathway.

Claudin-1 is important for the barrier function and growth of hair.