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Rare genetic variants in five specific genes are linked to male-pattern hair loss but only account for a small part of the risk.

A girl with a rare genetic condition affecting hair and nails also developed a common type of hair loss, suggesting a possible genetic link.

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

The gene Foxn1 is important for hair growth, and understanding it may lead to new alopecia treatments.

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.

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 Rotterdam Study found risk factors for elderly diseases, links between lifestyle and genetics with health conditions, and aimed to explore new areas like DNA methylation and sensory input effects on brain function.

Stem cell niches are crucial for regulating stem cell behavior and tissue health, and their decline can impact aging and cancer.

Alopecia areata is an autoimmune condition causing hair loss, influenced by genetics, stress, and diet, and may be prevented by a high soy oil diet.

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.

The document concludes that more research is needed to better understand and treat primary cicatricial alopecias, and suggests a possible reclassification based on molecular pathways.

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

A new gene, JMJD1C, may affect testosterone levels in men.

Aromatase gene variation may increase female hair loss risk.

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.

Cancer development is like natural selection, involving mutated cells and environmental factors.

Hair loss gene found on chromosome 3q26.

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

The document explains different types of hair loss, their causes, and treatments, and suggests future research areas.

DNA variants can predict male pattern baldness, with higher risk scores increasing baldness likelihood.