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

Blocking a specific enzyme can reduce the negative impact of stress hormones on hair growth cells.

African American women have a higher risk of preterm delivery than Caucasian women, and inflammatory stimuli affect gene expression in cells related to PCOS, showing a heightened inflammatory state in women with PCOS.

The balance between androgen receptor and p53 is crucial for sebaceous gland differentiation.

Pigs without the Hairless gene showed skin and thymus changes, useful for studying human hair disorders.

A certain genetic variation in the IL1A gene may lower the risk of a hair loss condition in Chinese people.

Drosha and Dicer are essential for hair follicle health and preventing DNA damage in skin cells.

The document concludes that scalp health is influenced by complex factors affecting sebaceous glands, including hormones, aging, and various substances.

The EDAR gene greatly affects hair thickness in Asian populations.

Congenital Adrenal Hyperplasia is a rare inherited disease causing hormone imbalances, affecting growth, fertility, and heart health, diagnosed through blood tests and treated with medication and lifestyle changes.

New research suggests that skin cell renewal may not require a special type of cell previously thought to be essential.

The review found no clear link between vitamin D receptor gene variations and polycystic ovary syndrome.

New tools show that in fish, NPY increases feeding and somatostatin decreases it.

A gene called HDAC9 might be a new factor in male-pattern baldness.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

Boys with less severe EDA mutations in XLHED have milder symptoms and better sweat and hair production.

Oxidative stress is a key factor in the development of Polycystic Ovary Syndrome, and weight management can improve symptoms.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

Eating fewer calories improves the ability of stem cells to repair and renew the body in various tissues.

Testing for CAG repeat polymorphism in the androgen receptor gene is not currently recommended for managing hypogonadism.

The document concludes that accurate diagnosis and treatment are crucial in dermatology, and it presents various findings on skin conditions and treatments.

Genetic data can predict male-pattern baldness with moderate accuracy, especially for early-onset cases in some European men.

Longer GGN repeats in the androgen receptor gene are linked to polycystic ovary syndrome.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

Genetics play a role in acne, but how exactly they contribute is not fully understood.

Altered retinoid metabolism in cicatricial alopecia suggests a balanced vitamin A diet may prevent the condition.

The L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.

In Singapore, most skin reactions to drugs were in females and Chinese, often caused by painkillers, antibiotics, and some other drugs, with serious cases linked to genetics.

Mice without certain skin enzymes have faster hair growth and bigger eye glands.

Certain gene patterns in breast cancer are linked to how active hormone receptors are and could affect patient survival.