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The research found that male pattern hair loss is mostly genetic and involves hair thinning due to hormonal effects and changes in gene expression.

Different ACE2 gene versions may affect COVID-19 impact based on age and suggest some hair loss drugs could be potential treatments.

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

The conclusions are: fecal short-chain fatty acids may help prevent cancer, fiber intake can reduce obesity, weight loss is hard for obese people, low BMI cancer patients are more prone to chemotherapy side effects, intermittent fasting benefits gut health, cherry laurel has health benefits in rats, certain gene variations can increase stress in hair loss patients, fecal acids can affect blood sugar levels, cold agglutinin can affect blood test results in autoimmune patients, and people with Crohn's disease have higher levels of a certain chemical in their blood.

Lhx2 is a crucial regulator of the Sonic Hedgehog signaling in early mouse retinal development.

The JAK/STAT pathway is important in cell processes and disease, and JAK inhibitors are promising for treating related conditions.

New method finds genetic links between Type 2 Diabetes and Prostate Cancer not seen before.

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

Nagashima-type palmoplantar keratosis in Asians is caused by a SERPINB7 gene mutation.

An American Bully with a genetic skin condition improved significantly with specific topical treatments.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

Genomic research can help improve the quality and production of natural fibers in animals.

Ficus benghalensis leaf extracts can effectively promote hair growth and inhibit hair loss.

Genetic factors and diet significantly increase the risk of male pattern baldness.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

Epidermolysis bullosa simplex causes easily blistered skin due to faulty skin cell proteins, leading to new treatment ideas.

Wounded skin cells can revert to stem cells and help heal.

Hair follicles are normally protected from the immune system, but when this protection fails, it can cause hair loss in alopecia areata.

Calcineurin inhibitors, used in kidney transplants, can cause a wide range of side effects including kidney damage and other health issues.

There are two ways to start hair growth: one needs Stat3 and the other does not, but both need PI3K activation.

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

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.

Reducing Tyrosinase prevents mature color pigment cells from forming in mouse hair.

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

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

Activating Nrf2 can help protect against hearing loss.

Researchers found genes and genetic variants linked to sheep wool and skin wrinkles.

Bmpr2 and Acvr2a receptors are crucial for hair retention and color.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

PPARγ is essential for maintaining healthy skin, controlling inflammation, and ensuring proper skin barrier function.