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Dr. Rodney Sinclair uses a detailed grading system to diagnose female pattern hair loss, recommends daily spironolactone and minoxidil for treatment, and believes genetics play a role in the condition.

Two mouse mutations cause similar hair loss despite different skin changes.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

Genes and hormones cause hair loss, with four genes contributing equally.

The study found that variations in hair protein genes are likely due to evolutionary deletions or duplications.

K_ATP channel gene mutations are linked to heart diseases, but more research is needed to understand the connection and treatment potential.

Cantú syndrome is caused by mutations in the ABCC9 gene.

Finasteride treats enlarged prostate and hair loss, but may cause side effects in some patients.

The Foxn1 gene mutation causes hairlessness and immune system issues, and understanding it could lead to hair growth disorder treatments.

The meeting focused on understanding, diagnosing, and finding treatments for irreversible hair loss diseases.

Alopecia areata causes hair loss due to an immune attack on hair follicles, influenced by genetics and environment.

Removing myelin protein zero-like 3 in mice leads to better metabolism and resistance to obesity.

Cicatricial alopecia, a permanent hair loss condition, is mainly caused by damage to specific hair follicle stem cells and abnormal immune responses, with gene regulator PPAR-y and lipid metabolism disorders playing significant roles.

UVB is good for a skin condition in Asian kids, a lotion works for head lice, a drug helps with a skin blistering disorder, a foam reduces itchiness in skin inflammation, birthmarks can be more widespread, and criteria for a neurocutaneous disorder were agreed upon.

Betamethasone dipropionate reduced skin thickness, fish oil increased it, and combined treatment had no significant effect.

High levels of ST14 and TMEFF1 proteins in ovarian cancer are linked to worse patient outcomes and may be a new treatment target.

New genetic mutations linked to rare skin disorders were found in three newborns.

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

Human hair loss may have evolved to help increase brain size.

Some hair protein genes evolved early and were adapted for use in hair follicles.

Mutant mice help researchers understand hair growth and related genetic factors.

Hair keratin-associated proteins are essential for strong hair, with over 80 genes showing specific patterns and variations among people.

The document concludes that AFA should be considered in patients with acromegaly-like features but normal hormone levels, and more cases need to be identified to understand the condition fully.

Low-coverage sequencing is a cost-effective way to identify genes related to wool traits in rabbits.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

2011 dermatological research found new skin aging markers, hair loss causes, skin defense mechanisms, and potential for new treatments.

Alopecia areata is caused by immune system attacks on hair follicles, often triggered by viral infections.

A specific gene variation is linked to a higher risk of polycystic ovary syndrome in Caucasian women.

A specific RNA modification in cashmere goats helps activate hair growth-related stem cells.

Early detection and multidisciplinary treatment are crucial for managing Papillon-Lefévre syndrome.