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Beta-sitosterol has potential health benefits but needs more research to fully understand its effects and improve its use in treatments.

Loss of sebaceous glands and inflammation may contribute to the development of scarring alopecia.

Nanomaterials in biomedicine can improve treatments but may have risks like toxicity, needing more safety research.

Cheonggukjang may help prevent and manage various diseases and improve overall health, but its odor and safety concerns need addressing.

Liposomes show promise in cancer treatment by delivering drugs with less toxicity and improved effectiveness.

Sex hormones, especially estradiol, can change chicken feather shapes and colors.

Environmental factors like diet and vitamin levels, especially Vitamin D, can affect autoimmune diseases differently, with lifestyle changes potentially improving outcomes.

The document concludes that hair follicles have a complex environment and our understanding of it is growing, but there are limitations when applying animal study findings to humans.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

Current treatments for hair loss from chemotherapy are limited, but new methods are being researched.

Alopecia areata is a reversible, autoimmune-related hair loss that can have significant emotional impact and uncertain treatment effectiveness.

Certain genetic variations in the FST gene are linked to better wool quality in Chinese Merino sheep.

Hair color is not a risk factor for developing alopecia areata.

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

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

A girl with a rare genetic condition affecting hair and nails also developed a common type of hair loss, suggesting a possible genetic link.

Adult mouse skin contains stem cells that can create new hair, skin, and oil glands.

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

iPSCs can help treat genetic skin disorders by creating healthy skin cells from a small biopsy.

Skin aging reflects overall body aging and can indicate internal health conditions.

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

Androgens affect hair growth and shedding, with genetic and non-genetic factors influencing baldness.

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

Birt–Hogg–Dubé syndrome is a rare genetic condition causing skin lesions, lung cysts, and a higher chance of kidney cancer.

The CUBIC protocol allows detailed 3D visualization of proteins in mouse skin biopsies.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

Hairlessness in mammals is due to complex genetic changes in both genes and regulatory regions.

The balance between cell renewal and differentiation controls the growth of cancerous cells in mouse skin.

TRPV3 could be a target for treating pain, skin disorders, and hair problems, but more research is needed to create effective drugs.

Scientists successfully created mouse hair proteins in the lab, which are stable and similar to natural hair.