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The TRPV3 gene variant may cause the long-haired suri alpaca coat.

Postpartum depression is linked to changes in brain chemicals, inflammation, stress, and certain genes, and can potentially be identified by markers like specific steroids, serotonin levels, and vitamin D levels.

A woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.

The machine learning model accurately predicts Systemic Lupus Erythematosus in Omani patients.

Hair growth serums A and C can affect hair growth genes and pathways, suggesting potential for personalized hair loss treatments.

The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.

Certain immune-related proteins are higher in people with alopecia and their healthy relatives, hinting at a genetic link.

The research suggests that Tourette syndrome is linked to both brain signaling and immune system pathways.

A new MBTPS2 gene variant disrupts fat metabolism and collagen production, causing Osteogenesis imperfecta.

Skin reactions to drugs are common and can be deadly, usually requiring stopping the drug and may be better prevented with genetic testing in the future.

Some blood-thinning medications can increase the risk of bleeding, and certain factors like genetics and other health conditions affect their safety and effectiveness.

Researchers found that certain RNA circles in the brain are linked to disease risk, but their exact role in disease is still unknown.

Karl E. Weick recommended focusing on everyday events and smaller organizations to improve organizational theory.

Karl E. Weick suggested focusing on everyday events and smaller groups to improve organizational theory and urged the inclusion of nonobvious aspects for better explanations.

PCOS is a common hormonal disorder in women that can be managed with lifestyle changes and various medications.

Mitochondrial dysfunction links metabolic syndrome and inflammatory skin diseases, suggesting targeted therapies and lifestyle changes.

There are still challenges in diagnosing and treating chronic skin diseases, but there is hope for future improvements.

Enzymes are classified into six types and are essential for many biological processes, with only a few targeted by drugs.

Hair follicle development in cashmere goats involves dynamic changes in proteins and metabolites, with key roles for oxytocin, MAPK, and Ca2+ pathways.

Forensic DNA Phenotyping can help predict physical traits from crime scene DNA to identify suspects.

Dermoscopy is useful for tracking alopecia areata treatment, with yellow dots and new vellus hairs being good indicators of hair regrowth.

Hormones and genetics play key roles in male and female baldness, which can affect mental health and may be linked to other health issues.

The 25Up study collected extensive data on mental disorders and related factors in Australian twins and siblings to investigate the genetics of psychiatric illnesses.

Women with PCOS often have skin problems like excessive hair, acne, hair loss, and dark patches, which can be treated with hormonal and non-hormonal therapies.

PCOS is a complex condition with major health impacts, needing more research for better diagnosis and treatment.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

The number of dermatologists in the US increased from 1995 to 2011, but they were unevenly distributed, mainly in urban areas, and areas with higher income and education levels.

The PIP5K1A gene helps cashmere growth in goats by promoting cell proliferation, and melatonin boosts its expression.

Hair follicles in mutant mice self-organize into ordered patterns within a week.

OCIAD2 and DCN genes affect hair growth in goats by having opposite effects on a growth signaling pathway and inhibiting each other.