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Men are more likely to get infectious skin diseases, while women are more prone to autoimmune and pigment-related skin conditions, influenced by biological and environmental factors.

Certain DNA variants can predict straight hair in Europeans but are not highly specific.

Patients with GATA2 deficiency show early skin symptoms that help diagnose the condition.

Genes linked to fibrosis are more active in people with central centrifugal cicatricial alopecia.

The meeting focused on understanding, diagnosing, and finding treatments for irreversible hair loss diseases.

The conclusion is that primary scarring alopecia is a complex condition that requires early and accurate diagnosis for effective treatment.

Hair follicle regeneration may slow tumor growth.

Deleting the Far2 gene in mice causes sebaceous gland issues and patchy hair loss.

The conclusion is that a thorough approach is needed to diagnose and manage hyperandrogenism in teenage girls, recognizing its major psychological and health effects.

Haplogroup X found in Altaian population supports Amerindian origin.

Two siblings both had a rare case of alopecia areata at the same time.

Most children with a common hemochromatosis genotype had elevated iron levels but no severe symptoms.

Nutrease powder, a high-protein, low-carb supplement, can help manage Polycystic Ovary Syndrome symptoms, regulate periods, improve ovulation, and restore fertility.

Certain miRNAs might be involved in a hair loss condition called frontal fibrosing alopecia and could possibly help in its diagnosis.

Some chemicals can permanently or temporarily remove color from skin and hair, which can be distressing and is not well-regulated in cosmetics.

Topical treatments led to hair regrowth in a man with linear morphea.

Testosterone significantly affects urination differences between male and female mice.

Fat-related cells are important for initiating hair growth.

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.

The research found that PCOS has common genetic factors regardless of how it is diagnosed and is linked to metabolic and reproductive issues.

Increasing mir-302 turns human hair cells into stem cells by changing gene regulation and demethylation.

Human skin makes sexual hormones that affect hair growth, skin health, and healing; too much can cause acne and hair loss, while treatments can manage these conditions.

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 research shows that a gene called Wnt3 affects hair growth and structure, causing short hair and balding when overactive.

The Rotterdam Study updated its design and objectives in 2012, providing insights into various diseases in the elderly, including skin cancer, bone health, liver disease, neurological and psychiatric conditions, and respiratory issues.

Creating stronger blockers for skin enzymes might lead to better treatment for conditions like acne and excessive hair growth.

The Rotterdam Study aims to understand various diseases in older adults.

Lactate production is important for activating hair growth stem cells.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.