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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.

A specific group of skin stem cells was found to help maintain hair follicle cells.

Sox2 controls hair color by affecting pigment production in hair follicles.

Androgens like testosterone may help treat traumatic brain injury by reducing mitochondrial stress and inflammation.

Sex hormones' effects on COVID-19 are unclear and more research is needed to understand their potential as treatment.

Autophagy prevents early aging and maintains lipid and pheromone balance in mouse glands.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

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

PCOS causes infertility mainly due to hormonal imbalances, insulin resistance, and chronic inflammation.

ATP-sensitive K+ channel subunits, particularly Sur2A, play a significant role in various cancers.

Keratin protein production in cells is controlled by a complex system that changes with cell type, health, and conditions like injury or cancer.

The protein STAT3 slows down cell growth by blocking the FST gene, which affects hair development in sheep.

Polycystic ovary syndrome and iron overload share similar symptoms and can be potentially treated with blood removal, diet changes, and probiotics.

Some women with PCOS have rare genetic variants linked to the condition.

PRP helps skin heal, possibly through special cells called telocytes.

CRABP2 helps increase the growth of cells important for hair growth by activating a specific growth pathway.

Certain genetic markers linked to wool quality in Rambouillet sheep were identified, which can guide better breeding choices.

The Msx2 gene affects feather development in Hungarian white geese and a specific gene variation could indicate feather quality.

Prdm1 is necessary for early whisker development in mice but not for other hair, and its absence changes nerve and brain patterns related to whiskers.

FGF12 is important for hair growth and could be targeted for hair loss treatment.

Certain genes related to sulfur metabolism are more active during the growth phase of Cashmere goat wool, and melatonin might help this process.

Fewer GGC sequences in the androgen receptor gene improve finasteride treatment for hair loss.

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

Editing the FGF5 gene in sheep increases fine wool growth.

FGF5 spliceosomes inhibit rabbit hair growth by affecting gene expression.

Excessive blue light harms eye cells and disrupts sleep patterns.

Three specific genetic variants cause severe skin issues in children with EBS, highlighting the need for early genetic screening.

Meis2 is essential for touch sensation and proper nerve connection to touch receptors in certain skin areas of mice.

Natural compounds from Chinese herbs may safely promote hair growth and treat common hair loss.

The KRT84 gene is linked to better wool quality in Gansu Alpine Fine-wool sheep.