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Over half of the children had abnormal hair under a microscope, with many having genetic hair conditions.

A specific genetic deletion in goats affects cashmere yield and thickness.

Dutasteride effectively treats benign prostatic obstruction, improves urinary flow, reduces prostate size, and may prevent prostate cancer, but can cause sexual side effects.

BAF200 is essential for proper heart and coronary artery formation.

TGFα gene mutation in mice causes abnormal skin, wavy hair, curly whiskers, and sometimes eye inflammation.

The 14-3-3σ gene is essential for preventing hair loss.

The CD4 protein may play a role in the behavior of certain skin cells, affecting their growth, movement, and differentiation.

A mouse gene mutation increases the risk of skin cancer.

Mutations in NIPAL4 cause skin issues by disrupting lipid layers, but some improvement is seen with topical treatment.

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.

The we/we wal/wal mice have defects in hair growth and skin layer formation, causing hair loss, useful for understanding alopecia.

A specific mutation known for causing cancer is also found to cause a skin condition in a young girl.

TSC2 is crucial for proper hair follicle development and patterning.

Mice lacking the PPARγ gene in their fat cells had almost no fat tissue, severe metabolic problems, and abnormal development of other fat-related tissues.

Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.

FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

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.

Removing anthrax toxin receptor 1 in pigs prevents Senecavirus A infection and causes a rare disease similar to GAPO syndrome.

Women with non-classical congenital adrenal hyperplasia have higher levels of certain steroids, which can be reduced by treatment.

WWOX deficiency in mice causes skin and fat tissue problems due to disrupted cell survival signals.

A new therapy for a skin blistering condition has not been developed yet.

Genomic profiling for myeloid cancers can find important inherited mutations, but it's challenging when these mutations aren't related to the patient's symptoms.

mEphA1 receptor tyrosine kinase is important for skin and hair development and may play a role in certain diseases.

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

Hair follicles are complex, dynamic mini-organs that help us understand cell growth, death, migration, and differentiation, as well as tissue regeneration and tumor biology.

The document concludes that understanding how the skin's immune system and inflammation work is complex and requires more research to improve treatments for skin diseases.

YAP and TAZ are crucial for skin cell growth and repair.

The Rotterdam Study updated its design and objectives in 2012, providing insights into various diseases in the elderly, including skin cancer, bone health, liver disease, neurological and psychiatric conditions, and respiratory issues.

AGA causes hair loss by shrinking hair follicles due to DHT binding, and can be treated with finasteride and minoxidil.