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Loss of a specific protein in skin cells causes symptoms similar to psoriasis.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

Macrophage iron release is crucial for hair growth and wound healing.

Keratin proteins are essential for keeping the cells in the human colon healthy and stable.

Melanoma's complexity requires personalized treatments due to key genetic mutations and tumor-initiating cells.

Rapamycin reduces age-related hearing cell loss in mice, but acarbose does not.

The 2015 Hair Research Congress concluded that stem cells, maraviroc, and simvastatin could potentially treat Alopecia Areata, topical minoxidil, finasteride, and steroids could treat Frontal Fibrosing Alopecia, and PTGDR2 antagonists could also treat alopecia. They also found that low-level light therapy could help with hair loss, a robotic device could assist in hair extraction, and nutrition could aid hair growth. They suggested that Alopecia Areata is an inflammatory disorder, not a single disease, indicating a need for personalized treatments.

Alopecia areata is an autoimmune condition causing hair loss, influenced by genetics, stress, and diet, and may be prevented by a high soy oil diet.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

Certain gene patterns in breast cancer are linked to how active hormone receptors are and could affect patient survival.

Genetic variations in hair keratin proteins exist but don't significantly affect hair structure.

The document concludes that significant investment in agricultural innovation is necessary to achieve global food security and nutrition.

KCNQ potassium channels help control the sensitivity of touch receptors in the skin.

FPHL is a common, age-related, genetic hair loss with unclear causes and limited treatment options.

Lichen Planus is a less common condition affecting skin and mucous membranes, with various types and associated risk factors, challenging to diagnose, significantly impacts life quality, and may have a risk of cancerous changes in oral lesions.

The Rotterdam Study aims to understand various diseases in older adults.

Different types of skin cells have unique genetic markers that affect how likely they are to spread cancer.

New treatments for Alopecia Areata show promise but need to be more effective and affordable.

Mice with enhanced regeneration abilities may help develop new regenerative medicine therapies.

With careful management, people with congenital adrenal hyperplasia can have successful pregnancies and become parents.

Changes in testosterone and estrogen receptor genes can affect how men age, influencing body fat, hair patterns, and possibly leading to skin disorders.

Vav2 and Vav3 proteins help control skin stem cell numbers and activity in both healthy and cancerous cells.

Lupus is a complex disease that requires personalized treatment because it varies greatly between individuals.

Genetic screening for NUDT15 polymorphisms is crucial for patients taking azathioprine, especially in Asians.

The Wnt/β-catenin pathway is important for body functions and diseases, and targeting it may treat conditions like cancer, but with safety challenges.

GALT5 and GALT2 are important for plant growth and development because they help with protein glycosylation.

Cyclic nucleotide-gated channels are crucial for proper root hair growth and calcium balance in plants.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

Foxn1 gene regulation is crucial for thymus development but not for hair growth.