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Researchers found that certain RNA circles in the brain are linked to disease risk, but their exact role in disease is still unknown.

Blocking the ATX-LPA pathway may improve insulin sensitivity and mitochondrial function in obesity.

The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.

Mice without certain skin enzymes have faster hair growth and bigger eye glands.

Activin A and follistatin control when hair cells develop in mouse ears.

Rapamycin reduces age-related hearing cell loss in mice, but acarbose does not.

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.

EGFR helps control how hair grows and forms without needing p53 protein.

The KRTAP21-1 gene affects wool yield and can help improve wool production.

Removing the VDR gene in skin cells reduces their growth and affects hair-related genes.

Distinct β-catenin patterns are linked to cell growth, not cell death, in lung cancer.

Cathepsin L is essential for normal hair growth and development.

Blocking BMP signaling causes hair loss and disrupts hair growth cycles.

The document concludes that careful design of genetic fate mapping experiments is crucial for accurate cell lineage tracing in mice.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

ROR-alpha may increase the growth of certain breast cancer cells by boosting aromatase, which could affect breast cancer prognosis.

Chemotherapy significantly lowers Inhibin A levels in breast cancer patients.

The absence of functional sebaceous glands causes hair follicle destruction and scarring alopecia.

Biotin and biotinidase are essential to prevent health issues, and deficiencies require lifelong supplementation.

KCNQ potassium channels help control the sensitivity of touch receptors in the skin.

Androgens can cause hair growth in some areas but hair loss on the scalp.

A gene mutation causes woolly hair in a Syrian patient.

A new gene mutation may allow some piebaldism patients to regain skin color in white patches.

Stem cells help remove dead cells to keep tissues healthy by balancing cell replacement and clearance.

TRM21 helps control flavonoid production and root hair growth in Arabidopsis thaliana.

MOF controls skin development by regulating genes for mitochondria and cilia.

Methylated gene parts may cause finasteride-resistance in some enlarged prostate patients.

AGD1 is important for root hair development in Arabidopsis, working with phosphoinositide signaling and the actin cytoskeleton.

Researchers found 44 proteins that change during different hair growth stages and may be important for hair follicle function.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.