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A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

ICAM-1 helps regulate hair growth cycles and skin remodeling.

Sulforaphane from broccoli may help treat certain cancers, hormone issues, and hair loss.

Bmpr2 and Acvr2a receptors are crucial for hair retention and color.

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

Cantú syndrome is caused by mutations in the ABCC9 gene.

Low oxygen areas help maintain and protect blood stem cells by using a simple sugar breakdown process for energy and managing their activity levels.

Men are more likely to get infectious skin diseases, while women are more prone to autoimmune and pigment-related skin conditions, influenced by biological and environmental factors.

A specific RNA modification in cashmere goats helps activate hair growth-related stem cells.

Non-coding RNAs could help detect and treat radiation damage.

Prolactin contributes to hair loss by promoting hair follicle shrinkage and cell death.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

Prolactin affects hair growth cycles and can cause early hair follicle regression.

Researchers found a genetic region that influences the number of coat layers in dogs.

Prolactin affects when mice shed and grow hair.

Prolactin affects when mice shed and grow hair.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

Dutasteride, usually used for prostate issues and hair loss, could potentially treat Amyotrophic Lateral Sclerosis (ALS) due to its neuroprotective, antioxidant, and anti-inflammatory properties, but more testing is needed.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

Allergic reactions to blood thinners are rare but can be serious, requiring careful management and alternative treatments.

Genetic defects in testosterone production can cause hormonal and developmental disorders, and more research is needed to understand androgen regulation and develop safer treatments.

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

The document concludes that early diagnosis and treatment of Congenital Adrenal Hyperplasia are crucial for preventing serious health issues and improving patient outcomes.

The new anti-acne treatment HA-P5 effectively reduces acne by targeting two key receptors and avoids an enzyme that can hinder treatment.

A new gel containing minoxidil can treat hair loss effectively, potentially reducing side effects and improving treatment.

New genes and pathways are important for testosterone production and male sexual development.

Certain defective glucocorticoid receptor mutants move faster inside cell nuclei and work less effectively.

The R343H mutation in the VDR gene causes vitamin D-resistant rickets with alopecia by impairing specific gene activity.

Patient-derived melanocytes can potentially treat vitiligo by restoring skin pigmentation.

Human skin can be reconnected to nerves using stem cells, which may help with skin health and healing.