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A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

Chemokine signaling is important for hair development.

The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.

Post-finasteride patients show changes in gut bacteria, possibly causing various symptoms.

Ranitidine and finasteride lower TMAO levels, reducing heart and kidney damage by changing gut bacteria.

Disrupting the FGF5 gene in rabbits leads to longer hair by extending the hair growth phase.

SLFC can improve scalp health and reduce sensitive scalp symptoms.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

The gene Prss53 affects hair shape and bone development in rabbits.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

Increasing mir-302 turns human hair cells into stem cells by changing gene regulation and demethylation.

Fat cells in the skin help start healing and form important repair cells after injury.

MicroRNA-302 helps improve the conversion of body cells into stem cells by blocking NR2F2.

Different PIN proteins affect plant root hair growth by changing how auxin is transported.

A new gene mutation causes female pseudohermaphroditism due to glucocorticoid resistance.

Certain bacteria and fungi are linked to healthy scalps and dandruff, suggesting that the scalp's microbial balance affects its health.

Finasteride treatment in male rats causes long-lasting effects on depression-like behavior, brain cell growth, inflammation, and gut bacteria composition.

Two specific hair keratin genes are active during hair growth and decline as hair transitions to rest.

Immune cells help regulate hair growth, and better understanding this can improve hair loss treatments.

Ancient Chinese goats evolved cashmere-producing traits due to selective breeding, particularly in genes affecting hair growth.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

A specific DNA region is crucial for Foxn1 gene expression in thymus cells but not in hair follicles.

The osteopontin gene is active in a specific part of rat hair follicles during a certain hair growth phase and might affect hair cycle and diseases.

A mutation in the Adam10 gene causes freckle-like spots on Hairless mice.

Melatonin treatment increases a specific RNA in goat cells that boosts cashmere growth.

Hsc70 protein may influence hair growth by responding to androgens.

New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.