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Hairless mammals evolved quickly in both gene and non-gene areas related to skin and hair.

The conclusion is that obesity should be managed with a slow, balanced approach to diet and exercise, with medication and surgery as additional options, and education and access to care are important.

In vivo lineage labelling is better than in vitro methods for identifying and understanding stem cells.

Different types of long-lasting stem cells are responsible for the growth and upkeep of the mammary gland.

Scarring alopecias are complex hair loss disorders that require early treatment to prevent permanent hair loss.

Certain gene variations increase male hair loss risk, influenced by hormone levels.

The UD-PrOZA program successfully diagnosed 18% of adult patients with rare diseases, often using genetic testing.

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.

Changes in the HR gene have influenced hair growth and may lead to hair loss conditions in humans.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

Certain immune cells are linked to non-scarring hair loss, suggesting potential for immune-targeted treatments.

Rare genetic variants in five specific genes are linked to male-pattern hair loss but only account for a small part of the risk.

Plant extracts may help prevent or reverse hair graying.

People with Major Depressive Disorder have a higher chance of getting Alopecia Areata, and vice versa; antidepressants may lower this risk.

A Saudi individual initially identified as a girl had a genetic disorder affecting gender development.

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

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

Mutations in the RBPJ gene cause Adams-Oliver Syndrome.

The conclusion is that teeth, hair, and claws have similar stem cell niches, which are important for growth and repair, and more research is needed on their regulation and potential markers.

Hair follicle stem cells are key for hair and skin regeneration, can be reprogrammed, and have potential therapeutic uses, but also carry a risk of cancer.

A family was found with both Trichorhinophalangeal syndrome and Loose Anagen Syndrome, suggesting a genetic connection.

Genetic mutations can affect female sexual development, requiring personalized medical care.

The study found that a specific genetic variation in the TNFα gene is significantly linked to Alopecia Areata in the Jordanian Arab population.

Kennedy's disease leads to muscle weakness without a cure, but exercise and managing symptoms may help patients live a normal lifespan.

People with Inflammatory Bowel Disease often lose hair due to stress, medication side effects, or lack of nutrients, and treatment depends on the specific cause.

Ancient Chinese goats evolved cashmere-producing traits due to selective breeding, particularly in genes affecting hair growth.

Researchers developed reliable models to predict how well certain compounds bind to androgen receptors, emphasizing the importance of atomic electronegativity.

Extracellular vesicles show promise for wound healing, but more research is needed to improve their stability and production.

The research found specific genes that may cause longer hair in Tianzhu White Yak.

Male pattern hair loss is genetic and influenced by hormones, with treatments like minoxidil and surgery available.