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Certain genetic variants in ERN1, TACR3, and SPPL2C are linked to when Alzheimer's disease starts.

Rare genetic variants in 125 genes are linked to male-pattern hair loss.

Hair pattern in androgenetic alopecia overlaps with scalp and bone demarcations, with distinct gene profiles affecting susceptibility.

Hair follicles are complex, dynamic mini-organs that help us understand cell growth, death, migration, and differentiation, as well as tissue regeneration and tumor biology.

Different types of long-lasting stem cells are responsible for the growth and upkeep of the mammary gland.

Changing the environment around stem cells could help tissue repair, but it's hard to be precise and avoid side effects.

Alopecia Areata is an autoimmune condition causing hair loss with no cure and treatments that often don't work well.

The Rotterdam Study updated findings on elderly health, focusing on heart disease, genetics, lifestyle effects, and disease understanding.

The skin's layers protect, sense, and regulate the body's internal balance, but can be prone to cancer.

The secretome from mesenchymal stem cells is a promising treatment that may repair tissue and avoid side effects of stem cell transplantation.

Future hair loss treatments should aim to extend hair growth, reactivate resting follicles, reverse shrinkage, and possibly create new follicles, with gene therapy showing promise.

Insulin resistance and obesity are key factors in the development and worsening of polycystic ovary syndrome, and lifestyle changes are important for managing it.

Women look young for their age due to larger lips, less sun damage, and genes that prevent gray hair and wrinkles.

Early diagnosis and individualized treatment improve outcomes for Congenital Adrenal Hyperplasia.

AGA more common in men, Koreans have lower rates and unique patterns.

Alopecia areata is an autoimmune disease causing patchy hair loss, often with other autoimmune disorders, but its exact causes are unknown.

A genetic defect in vitamin D receptors causes severe rickets and hair loss in children, but some heal as they age.

Methotrexate is a key, cost-effective drug for skin conditions, but requires careful monitoring for side effects.

Isotretinoin's effects and side effects, like birth defects and depression, might be due to it causing cell death in various cells.

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

New genetic discoveries may lead to better treatments for alopecia areata.

Hair loss gene found on chromosome 3q26.

Genetic differences between young and old Tan sheep explain why their fleece changes from curly to straight as they age.

Keratins are important for skin cell health and their problems can cause diseases.

New methods to improve the healing abilities of mesenchymal stem cells for disease treatment are promising but need more research.

Genetically modified plants could be an important source of omega-3 fats to meet global needs.

The document concludes that recognizing and properly diagnosing lipodystrophy syndromes is crucial for effective management and treatment.

Noggin gene inactivation causes skeletal defects in mice, varying by genetic background.

Effective management of children's hair loss involves accurate diagnosis, various treatments, and supportive care.

Human enzymes can detoxify harmful substances but might also increase their cancer risk.