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Vitamin E affects liver metabolism, enhancing stress resistance, reducing blood clotting, and altering hormone processing.

A certain genetic variation in the IL1A gene may lower the risk of a hair loss condition in Chinese people.

Human leukocytes and beard hair follicle cells have internal daily clocks, and PER1 and PER3 genes may indicate individual circadian rhythms.

Scientists made stem cells that can grow hair by adding three specific factors to them.

MOF controls key genes for skin development by regulating mitochondrial and ciliary functions.

Hair loss in Androgenetic alopecia (AGA) is due to altered cell sensitivity to hormones, not increased hormone levels. Hair growth periods shorten over time, causing hair to become thinner and shorter. This is linked to miscommunication between cell pathways in hair follicles. There's also a change in gene expression related to blood vessels and cell growth in balding hair follicles. The exact molecular causes of AGA are still unclear.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

The peach gene pCTG134 helps control the interaction between auxin and ethylene hormones during fruit ripening.

ATP-dependent chromatin-remodeling complexes are crucial for gene regulation, cell differentiation, and organ development in mammals.

A gene variation is linked to hair thickness in Asians.

Advancements in nanoformulations for CRISPR-Cas9 genome editing can respond to specific triggers for controlled gene editing, showing promise in treating incurable diseases, but challenges like precision and system design complexity still need to be addressed.

Higher miR-34a levels and the A variant of the MIR-34A gene are linked to increased risk and severity of alopecia areata.

An individual's morning or evening preference can predict changes in their body clock gene expression.

Liposomes show promise for delivering CRISPR for gene editing but face challenges like delivery efficiency and safety concerns.

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

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

The article concludes that better understanding gene regulation related to seasonal changes can offer insights into the mechanisms of seasonal timing in mammals.

SOX9 helps determine stem cell roles by interacting with DNA and proteins that control gene activity.

JAK inhibitors may help treat Alopecia Areata but need careful monitoring due to side effects.

Different human traits like skin color and hair type vary between populations due to genetic adaptations to the environment.

Six new genetic regions linked to early hair loss also connect to Parkinson's disease and prostate cancer, possibly leading to new treatments.

Researchers found 63 genes linked to male-pattern baldness, which could help in understanding its biology and developing new treatments.

New targeted therapies for hair loss from alopecia areata show promise, with personalized treatment expected in the future.

CRISPR/Cas9 gene-editing shows promise for improving sheep and goat breeding but faces challenges with efficiency and accuracy.

New method uses hair follicle cells to estimate human body clock phase, potentially improving sleep disorder diagnosis.

Researchers found four genes that could help diagnose severe alopecia areata early.

DNA changes in tetraploid wheat improve root growth and nitrogen use.

Exosomes from dermal papilla cells help hair growth by making hair follicle stem cells multiply and change.

Vitamin A may influence hair loss conditions like alopecia, but more research is needed to understand how.

CD2 might be a new treatment target for patchy alopecia areata.