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

Combining minoxidil and plant extracts improved hair growth in a boy with a rare genetic disorder.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

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.

Notch signaling disruptions can cause various skin diseases.

Studying premature aging syndromes helps understand human aging and suggests potential treatments.

Seaweeds contain beneficial compounds with potential uses in food, cosmetics, and health, but more research is needed to improve extraction and safety.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

A gene mutation in mice causes increased mast cells and disorganized hair follicles in their skin.

Understanding keratinization is crucial for treating skin conditions like ichthyoses and psoriasis.

Cobalt is important for health but too much or too little can cause health problems, and its environmental buildup is a concern.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

Preventing cancer involves lifestyle changes, vaccinations, early screening, and understanding cancer's molecular basis.

Organoids help study and treat genetic diseases, offering personalized medicine and therapy testing.

Genetic analysis of rabbits identified key genes for traits like coat color, body size, and fertility.

Vitamin C and E may help with certain skin and hair conditions, but more research is needed to confirm their effectiveness.

Sodium valproate caused vomiting in 20% of children under 2 years old, with other side effects like hair loss and loss of appetite also noted.

A woman's new seizures were caused by a brain tumor likely linked to her past cancer treatment, and choosing safe seizure medications is important for women who can have children.

NEMO syndrome and systemic lupus erythematosus are linked in a new disease association.

SA linked to mitochondrial issues and oxidative stress, while AGA involves disrupted hair growth genes.

The document concludes that dermatology training and grading scales need to better represent dark-skinned individuals to improve diagnosis and assessment of skin conditions.

Obese mice with a leptin gene mutation have a longer resting phase in their hair cycle, which may help understand certain hair loss conditions.

Noggin overexpression delays eyelid opening by affecting cell death and skin cell development.

MicroRNA-214 is important for skin and hair growth because it affects the Wnt pathway.

Hairless mice lack fur due to a genetic mutation affecting skin response, not hormone issues.

Rapamycin treatment helps with mitochondrial disease by reducing PKC levels.

Mitochondrial problems in tooth cells lead to bad enamel and dentin development in mice.

Borneol Essential Oil could be a natural and safe acne treatment.

Exposure to finasteride in the womb caused lasting reproductive issues in male rats.