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Monotreme hair structure and protein distribution are similar to other mammals, but their inner root sheath cornifies differently, suggesting a unique evolution from reptile skin.

Some hair protein genes evolved early and were adapted for use in hair follicles.

Two patients with the same genetic mutation had both blistering skin and easily pulled out hair.

SP1 promotes and KROX20 inhibits hair cell growth by affecting the CUX1 gene.

Rac1 is essential for proper hair structure and color.

Genetic defects and UV radiation cause skin damage and aging.

Mice without the vitamin D receptor have bone issues and other health problems, suggesting vitamin D is important for preventing various diseases in humans.

Certain genes and pathways are linked to the production of finer and denser wool in Hetian sheep.

Estrogen therapy helped regrow hair in a bald man.

People with pattern hair loss have higher polyamine levels in the top of their head compared to the back.

Specialized ribosomes affect aging in human skin cells.

A woman's hair turned gray and fell out after starting a cancer drug called imatinib mesylate.

The document concludes that Loose Anagen Hair Syndrome is a benign condition where hair is thin and easily pulled out, often improving with age.

Researchers found genes linked to feather growth speed in Shouguang chickens, highlighting two genes that might explain differences in feathering.

FGF9 helps hair follicles grow in small-tailed Han sheep by affecting cell growth and certain signaling pathways.

DNA methylation controls lncRNA2919, which negatively affects hair growth.

New hair follicles could be created to treat hair loss.

Exosomes could be key in treating skin conditions and healing wounds.

Finasteride may cause lasting sexual and mental health issues, and genetic screening could help prevent them.

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

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

The Gsdma3 gene is essential for normal hair development in mice.

Keratin 17 is linked to various diseases, including cancer and skin conditions, and may be a target for diagnosis and treatment.

Some cells may slow melanoma growth, a protein could affect skin pigmentation, a gene-silencing method might treat hair defects, skin bacteria changes likely result from eczema, and a defensin protein could help treat multiple sclerosis.

A gene mutation causes early keratinocyte maturation leading to hair loss in Olmsted syndrome.

The study concluded that PKP1 is essential for skin integrity and hair growth, and its dysfunction causes the symptoms of ectodermal dysplasia/skin fragility syndrome.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

A girl with a rare skin condition improved after one month of treatment with acitretin.

Trichothiodystrophy hair is structurally abnormal with protein and organization issues.

VEGF helps squamous cell carcinoma grow in ways beyond just blood vessel formation.