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Hair follicle sampling is a practical method for measuring biomarkers in children with and without Fragile X syndrome.

The document concludes that insulin resistance is key in PCOS development and early treatment is crucial to prevent complications.

Ancient Chinese goats evolved cashmere-producing traits due to selective breeding, particularly in genes affecting hair growth.

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

Harlequin mutant mice have hair loss due to low AIF protein levels and retroviral element activity.

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

Testosterone significantly affects sexual desire in both men and women, but its impact on women is more complex and influenced by psychological factors.

New treatments for prostate cancer and BPH show promise, including novel compounds that target hormone synthesis and response.

Diagnosing sex development disorders requires combining medical history, physical exams, imaging, lab tests, and genetic data.

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

Selective breeding can enhance immunity in dairy cattle.

Hair loss from Alopecia Areata is caused by both genes and environment, with several treatments available but challenges in cost and relapse remain.

Certain gene variations and irregular X chromosome activity may contribute to hair loss in women who can have children.

Dermatologists give better information on pathology forms, hypersensitivity vasculitis is a common skin issue, misdiagnoses can occur, and various skin conditions are linked to loss of elastin or genetic factors.

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

Hair follicle sampling is a feasible method to measure FMRP and FMR1 mRNA levels in children.

Protoporphyrin IX is useful in cancer treatment but can cause health problems if not properly regulated.

Skin abnormalities can indicate immunodeficiency due to shared origins with the immune system.

Different types of long-lasting stem cells are responsible for the growth and upkeep of the mammary gland.

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

The conclusion is that many small genetic variations influence claw disorders in cows, and using genomic selection could help reduce these disorders.

G allele of AR Stul polymorphism linked to higher hair loss risk, especially in white people.

Ancient DNA blocks are still present in human genomes, possibly due to advantages they provide.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

Androgen is important in controlling stem cell differentiation, reducing fat development, and increasing lean mass.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

New treatments for male hair loss show promise but need more research for safety and effectiveness.

Women with hair loss have more androgen receptors in certain hair follicles.

Early-onset baldness is linked to genetics, lifestyle, and can indicate higher risk for heart and metabolic diseases, and affects mental health.

Changes to the Foxp3 protein affect how well regulatory T cells can control the immune system, which could help treat immune diseases and cancer.