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Astilbin can potentially calm overactive immune responses, like in Type 1 Diabetes, by suppressing certain cell activities and reducing inflammation.

DHEA affects multiple receptors and may help with metabolic issues, but its safety and effectiveness in humans are unclear.

HOXC13 is essential for hair and nail development by regulating Foxn1.

Four patients with a type of rickets and hair loss had different mutations in their vitamin D receptor gene, causing it to not work properly.

Aloe vera fermentation helps heal burns faster by reducing inflammation and changing gut bacteria.

Researchers found a specific immune receptor in patients that causes severe skin reactions to a drug.

DNA profiling in forensics has improved, but predicting physical traits and ancestry from DNA has limitations and requires ethical consideration.

The timing of when the gene Bmal1 is active affects aging and survival, with its absence during development, not adulthood, leading to premature aging.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

Human hair follicles can make and process prostaglandins, which may affect hair growth.

Certain microRNAs are more common in balding areas and might be involved in male pattern baldness.

AIRE-deficient rats developed severe autoimmune disease similar to APECED, useful for testing treatments.

lncRNA2919 slows down rabbit hair growth by stopping cell growth and causing cell death.

Annexin A2 isoform 2 helps dermal papillae cells grow, affecting hair growth.

A boy with toxic shock syndrome had severe heart rhythm problems but recovered with treatment.

Gene differences may affect baldness treatment response in Korean men.

Short telomeres contribute to aging and cancer, and while telomerase can delay aging, it may also promote cancer.

FP-1 is a key protein in rat hair growth, active only during the growth phase.

Longer GGN repeats in the androgen receptor gene are linked to polycystic ovary syndrome.

CDP is crucial for lung and hair follicle cell development.

A WNT10A gene mutation leads to ectodermal dysplasia by disrupting cell growth and differentiation.

TCDD speeds up skin barrier formation by increasing certain gene expressions.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

Genetic screening is crucial for accurately diagnosing APS-1 due to its varied symptoms.

Brg1 is crucial for hair growth and skin repair by maintaining stem cells and promoting regeneration.

Vitamin D3 analogs can promote hair growth in mice genetically prone to hair loss.

Oncogenic K-ras causes rapid cancerous changes in the mouth's lining.

AGD1's PH domain is essential for its role in root hair growth and polarity.

Dynamic, light touch is sensed through a common mechanism involving Piezo2 channels in sensory axons.

NAC1 controls certain enzymes that reduce root hair growth in Arabidopsis.