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Certain gene variants can cause inherited hair diseases, which are important to diagnose and understand for patient care.

Scalp psoriasis features reversible hair loss and specific immune activation, with no significant hair follicle damage.

Adding soybean oil to Nonomuraea dietziae increases production of a beneficial compound by improving metabolism and enzyme systems.

m-Aminophenol in hair dye can cause skin cell toxicity and stress responses.

Deregulation of stem cell function is central to the development of some cancers.

Androgenetic alopecia is mainly caused by genetic factors and increased androgen activity, leading to hair follicle miniaturization.

CAH is a genetic disorder affecting cortisol production and causing hormonal imbalances, with treatment and diagnosis varying by form and symptoms.

Hair loss in men might be linked to changes in cell energy factories.

Reproductive hormones play a crucial role in breast cancer development and treatment challenges.

Congenital Adrenal Hyperplasia is a rare inherited disease causing hormone imbalances, affecting growth, fertility, and heart health, diagnosed through blood tests and treated with medication and lifestyle changes.

Prostaglandin D2 increases testosterone production in skin cells through a process involving reactive oxygen species, which could be a new target for treating hair loss and other skin conditions driven by testosterone.

Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.

New genetic insights have improved understanding of hair loss, leading to a new test and treatments, but more research is needed on the test and laser comb effectiveness.

Topical minoxidil may help treat a rare genetic hair condition with no fully effective treatments yet.

Some conditions mimic PCOS symptoms and need careful diagnosis to treat potentially serious health issues.

Bardet-Biedl syndrome may include under-recognized skin problems related to its metabolic disturbances.

HIF-1α is important for hair growth and could be a treatment target for hair loss.

Environmental factors like smoking, UV exposure, and poor diet contribute to hair loss and graying, and lifestyle changes can help manage it.

RNA editing significantly affects hair growth and follicle cycling in the Tianzhu white yak.

New methods can diagnose hair loss by examining the scalp and can treat it with a mix of oral and topical medications, along with cosmetic procedures like hair transplants.

Most women with excess hair growth have an underlying hormonal issue, often treated with medication and hair removal methods.

Olive leaf compound oleuropein helps grow hair in mice.

The document concludes that Follicular Unit Extraction is an advanced, less invasive hair transplant method with fewer side effects than traditional methods.

Low-coverage sequencing is a cost-effective way to find genetic factors affecting rabbit wool traits.

A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

The KRTAP7-1 gene is very similar across different cattle and yak breeds and likely plays a role in hair strength and shape.

The research mapped gene activity in developing mouse skin and found key markers for skin cell types and changes from fetal to early postnatal stages.

A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

Alopecia in patients with epidermolysis bullosa varies in severity and is often caused by skin blistering or trauma.