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Certain gene variations may increase the risk of hair loss in Egyptians.

The study suggests certain ACE gene variations are more common in women with PCOS and may be linked to increased insulin resistance.

Certain gene mutations are linked to wool quality in sheep and could help in breeding for better wool.

Different ACE2 gene versions may affect COVID-19 impact based on age and suggest some hair loss drugs could be potential treatments.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

The AUTS2 gene is linked to neurological disorders and may affect human brain development and cognition.

Nonclassic congenital adrenal hyperplasia is a genetic disorder causing hormone imbalances, affecting fertility and requiring personalized treatment.

Patients with myotonic dystrophy often have skin problems that suggest early aging and vitamin D issues, and the severity of these problems is linked to their genetic condition and vitamin D levels.

YAP and TAZ proteins are necessary for the development of two types of skin cancer.

Certain gene variations in the Vitamin D Receptor are linked to higher risk of female hair loss.

The enzyme 25 Hydroxyvitamin D 1 α-Hydroxylase is essential for healthy skin and recovery after skin damage.

Alopecia areata is likely caused by a combination of genetic factors and immune system dysfunction, and may represent different diseases with various causes.

Hairless gene not strongly linked to baldness.

Beige and leaden pigment genes act within melanocytes, affecting pigment patterns.

A genetic variant in the androgen receptor gene increases heart disease risk in women but not in men.

Longer TA repeats in the SRD5A2 gene may increase acne risk in Chinese people.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

Certain genes influence immunoglobulin levels in Chinese Holstein cows, which can improve calf health.

Selective breeding can enhance immunity in dairy cattle.

Mice without the vitamin D receptor have bone issues and other health problems, suggesting vitamin D is important for preventing various diseases in humans.

The Rotterdam Study investigates diseases in older adults and has produced many research findings.

The vitamin D receptor is crucial for bone health and affects various body systems, with mutations potentially leading to disease.

Male hormones may play a role in the development of heart disease, and more research is needed to understand their effects.

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

The study found that in Latin America, ancestry varies by location, influences physical traits, and affects how people perceive their own heritage.

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.

TRPA1 is crucial for mechanical sensitivity in skin sensory neurons.

Removing part of the vitamin D receptor stops vitamin D from working properly.

The Rotterdam Study aims to understand disease causes in the elderly and has found new risk factors and genetic influences on various conditions.

Exposure to too much androgen before birth might cause polycystic ovary syndrome later in life.