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Mutations in the NR3C1 gene cause a rare condition that affects hormone signaling and can lead to various symptoms, with dexamethasone as a treatment option.

LIPH mutations in Japan cause varying degrees of hair loss and woolly hair.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

The genes KRT25 and SP6 affect curly hair in horses, with KRT25 also causing hair loss. If both genes are mutated, the horse gets curly hair and hair loss. KRT25 can hide the effect of SP6.

Scientists successfully edited a goat's genes to grow more and longer cashmere hair.

Female pattern hair loss has multiple causes and treatments, with new therapies showing promise.

A vitamin D receptor mutation causes rickets and affects immune responses.

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

Researchers identified a new variant of the FGF5 gene in sheep that affects hair length.

Epidermolytic ichthyosis can be inherited in a semidominant way with mild symptoms in carriers.

Melatonin affects gene expression in goat hair follicles, potentially increasing cashmere production.

Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.

LGR5 is a common marker of hair follicle stem cells in different animals and is important for hair growth and regeneration.

The research found genes that change during cashmere goat hair growth and could help determine the best time to harvest cashmere.

UV exposure reduces Lgr6+ stem cells in mouse skin and they don't significantly contribute to skin cancer development.

Overexpression of HDGF in melanocytes does not cause cancer.

AE can have varied symptoms and genetic causes, but zinc therapy helps.

A specific gene mutation causes long hair in Angora rabbits.

Certain microRNAs are important for sheep hair follicle development and could help improve wool quality.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

White blood cells and their traps can slow down the process of new hair growth after a wound.

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

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.

Scientists found new genetic areas that affect how rice root hairs grow and develop.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

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

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

Mutations in specific llama genes may affect fiber quality for textiles.