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Women who had bariatric surgery risk nutritional deficiencies causing skin issues during pregnancy and breastfeeding.

Taxol damages hair growth cells, causing hair loss.

Mutations in Plcd1 and Plcd3 together cause severe hair loss in mice.

BMP4-related anomalies can cause a wide range of eye, brain, and hand/foot problems, and new cases show this variability.

OCIAD2 and DCN genes affect hair growth in goats by having opposite effects on a growth signaling pathway and inhibiting each other.

The document concludes that periocular hair disorders have various causes and treatments, and proper evaluation by specialists is important for management and prognosis.

Testosterone is crucial for development, growth, and various body functions in mammals.

Most hair loss in children is caused by a few common conditions and is easy to diagnose, but rare types require careful evaluation.

Indian Gooseberry has potential for cancer prevention and treatment and promotes hair growth.

Three siblings with a genetic form of rickets showed different symptoms of the disease.

The review highlights the importance of stem cells in hair health and suggests new treatment strategies for hair loss conditions.

Inhibiting ALOX12 can help hair cuticle maturation by increasing S100A3 citrullination.

PNKP is essential for keeping adult mouse progenitor cells healthy and growing normally.

The document describes various skin conditions, their features, and treatments but lacks detailed study size information.

Gray hair can potentially be reversed, leading to new treatments.

Certain long non-coding RNAs are important for the growth of hair follicles in Inner Mongolian cashmere goats.

Minoxidil does not work to inhibit lysyl hydroxylases in newborn mouse lungs.

A girl with Denys-Drash syndrome was misdiagnosed due to biotin affecting her hormone test results.

Differences in gene expression and methylation patterns found in AGA patients suggest potential targets for future treatments.

Pharmacy-sold shampoos tend to have fewer allergens compared to those sold in other stores.

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.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

Genetics, stress, and health issues can cause early hair greying, which affects self-esteem, and there's no cure, only hair dye.

The congress highlighted new gene therapy techniques and cell transplantation methods for treating diseases.

Most adrenal cortex tumors are benign and non-secreting, but proper diagnosis and treatment are important due to the rare possibility of cancer.

Early treatment of acne is crucial to prevent scarring and psychological effects.

Certain genetic variants linked to immune response increase the risk of alopecia areata in Taiwanese people.

Keratin gene expression helps understand different types of skin cells and their development, and should be used carefully as biological markers.

Father's finasteride use may affect son's fertility and testicular function.

Adequate vitamin D might lower, and high hair chromium might increase DNA damage in obese women.