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Hair growth is controlled by specific gene clusters and proteins, and cysteine affects hair gene expression in sheep.

Finasteride reduces Tourette syndrome symptoms, but results may be limited due to potential biases.

The conclusion is that androgen receptor gene polymorphism might be a marker for polycystic ovary syndrome, but more research is needed.

Longer CAG repeat lengths in the androgen receptor gene are linked to higher testosterone levels in women with PCOS.

Surface Plasmon Resonance is a useful tool for studying protein interactions and has potential for future technological advancements.

Basal cell carcinomas have much higher levels of Vitamin D3 receptors compared to healthy skin.

Kennedy's disease leads to muscle weakness without a cure, but exercise and managing symptoms may help patients live a normal lifespan.

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

Hormones during pregnancy and lactation keep skin stem cells inactive, preventing hair growth.

Finger length ratios are not linked to the number of specific gene repeats affecting testosterone sensitivity.

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

Finasteride may help reduce symptoms in male Tourette syndrome patients.

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

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

A male with aromatase deficiency improved bone health with estradiol treatment.

Non-coding RNAs play key roles in the hair growth cycle of Angora rabbits.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

Stress and alcohol affect brain chemicals differently in rats, mice, and humans, influenced by genetic differences.

ALA-PDT is effective and safe for chronic X-ray dermatitis, providing complete or partial remission.

New treatments for immune disorders caused by FOXN1 deficiency are promising.

Dutasteride makes alcohol less sedating and may lead to less drinking in men.

APS-1 in Italy shows diverse AIRE mutations and various autoimmune issues.

The document describes a woman with familial Parkinson's disease due to a genetic mutation, showing severe symptoms and poor response to treatment, and suggests finasteride may help reduce symptoms in Tourette syndrome.

Certain defective glucocorticoid receptor mutants move faster inside cell nuclei and work less effectively.

Mutations in the WNT10A gene can cause skin, hair, teeth, and other disorders, and may also affect other areas like kidney and cancer, with potential for targeted treatments.

Recent genetic insights show that low-renin hypertension includes a range from essential hypertension to secondary or familial forms, affecting diagnosis and treatment.

Hair disorders are caused by a complex mix of biology, genetics, hormones, and environmental factors, affecting hair growth and leading to conditions like alopecia.

The document concludes that careful design of genetic fate mapping experiments is crucial for accurate cell lineage tracing in mice.

WNT10A mutations cause varied symptoms in patients with odonto-onycho-dermal dysplasia.

A gene deletion causes the "hairless" trait in Iffa Credo rats.