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Shorter telomeres in white blood cells may increase the risk of a common type of hair loss.

The research showed how melanocytes develop, move, and respond to UV light, and their stem cells' role in hair color and skin cancer risk.

Skin lesions in Carney Complex are caused by a gene change in some skin cells that leads to increased pigmentation and may lead to tumors.

New models predict male pattern baldness better than old ones but still need improvement.

Two mutations in KRT74 and EDAR genes cause sheep to have finer wool.

The study found that the hair loss condition in Cesky Fousek dogs is influenced by multiple genes affecting skin and muscle structure, fat metabolism, and immunity.

Long-term high testosterone levels can improve bone density and reduce body fat but may increase the risk of prostate cancer and high blood pressure.

Autophagy helps control skin inflammation and cancer responses and regulates hair growth by affecting stem cell activity.

The TRPV3 ion channel is important for skin and hair health and could be a target for treating skin conditions.

Different versions of the KRTAP6-2 gene in goats can lead to thinner cashmere fibers.

The study concludes that regulating apoptosis could lead to new treatments for various skin and hair conditions.

Female cuckoo color differences are linked to their unique genes and help avoid male harassment.

The SOSTDC1 gene is crucial for determining sheep wool type.

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.

New CRISPR/Cas9 variants and nanotechnology-based delivery methods are improving cancer treatment, but choosing the best variant and overcoming certain limitations remain challenges.

The Msx2 gene affects feather development in Hungarian white geese and a specific gene variation could indicate feather quality.

Prdm1 is necessary for early whisker development in mice but not for other hair, and its absence changes nerve and brain patterns related to whiskers.

Vitamin D Receptor is crucial for hair follicle shrinkage and cell death, affecting hair growth.

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

The document concludes that more research is needed to reduce frequent hospital visits, addiction medicine education improves with specific training, early breast cancer surgery findings are emerging, nipple smears are not very accurate, surgery for older melanoma patients doesn't extend life, a genetic condition in infants can often be treated with one drug, doctors are inconsistent with blood clot medication, a certain gene may protect against cell damage, muscle gene overexpression affects many other genes, and some mitochondrial genes are less active in mice with tumors.

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

Afro-textured hair needs personalized care due to its unique genetic traits.

Docetaxel often causes hair loss, with limited effective treatments and no cure for permanent hair loss.

A new tool can analyze hair to detect changes due to hormones, genetics, and aging.

Activating TLR9 helps heal wounds and regrow hair by using specific immune cells.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

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

Editing the FGF5 gene in sheep increases fine wool growth.

Bimatoprost helps with hair growth and eye conditions but can be costly and have side effects.