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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.

Current treatments for Alopecia Areata have mixed success, and there's a need for better, more accessible options and support for affected individuals.

Alopecia areata is an autoimmune disease with genetic links, treatable with certain medications, and can affect mental health.

Dermal papilla cells can help regrow hair and are promising for hair loss treatments.

Multi-omics techniques help understand the molecular causes of androgenetic alopecia.

Editing the FGF5 gene in sheep increases fine wool growth.

Combination pharmacotherapy is generally more effective for treating keloids and hypertrophic scars.

Alopecia areata and vitiligo share immune system dysfunction but differ in specific immune responses and affected areas.

The study found that alopecia areata and hypothyroidism increase the risk of each other, but androgenetic alopecia and hypothyroidism do not.

New liposome treatment successfully delivers CRISPR to deactivate a key enzyme in androgen-related disorders.

A special gene region controls the re-emergence of a primitive wool type in Merino sheep, improving their wool yield and adaptability.

The BUZZ gene is important for root hair growth and overall root structure in the plant Brachypodium distachyon.

Different genes cause Female Pattern Hair Loss compared to male hair loss, and treatments vary, but more research is needed to understand it fully.

New understanding and treatments for hair loss are improving, but more research is needed.

Certain immune molecules and stress affect hair loss, and while genes play a role, more research is needed to fully understand and treat it.

IL-1α levels are higher in alopecia areata patients, suggesting a role in the disease.

The PON1 192R gene variant is linked to a higher risk of psoriasis and heart disease in Western Mexico.

Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

Eating a lot of fat increases PKCβ and inflammation in skin fat cells, which affects skin and hair health.

Researchers created a skin graft that senses blood glucose and could treat diabetes using CRISPR-edited stem cells.

Found new possible treatments for hair loss.

Isotretinoin's effects and side effects, like birth defects and depression, might be due to it causing cell death in various cells.

No link found between aromatase gene and female hair loss.

The A allele of the C2 gene increases the risk of lupus, while the G allele may protect against it.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

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

IL-4 gene variation may increase the risk of alopecia areata in Turkish people.

G allele of AR Stul polymorphism linked to higher hair loss risk, especially in white people.