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The length of CAG repeats in the androgen receptor gene is linked to ovarian reserve but does not affect how the ovaries respond to stimulation.

Transplant success has improved with better immunosuppressive drugs and donor matching.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

Finasteride treats enlarged prostate and hair loss, but may cause side effects in some patients.

DHT's role in hair loss is important, but measuring its level for diagnosis is questionable.

Skin symptoms can indicate endocrine disorders and have various treatments.

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.

Researchers found genes and genetic variants linked to sheep wool and skin wrinkles.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

Mild essential fatty acid deficiency can cause health issues and is worsened by low-fat diets.

Certain mutations in the H6PD gene cause Cortisone Reductase Deficiency by affecting hormone production.

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

Animals that change color with the seasons mainly do so in response to daylight changes, but climate change is causing camouflage problems that may require evolutionary changes.

The study concluded that immune cells attacking hair follicles cause hair loss in alopecia, with genetics and environment also playing a role, and highlighted the potential of certain treatments.

The document concludes that while some organisms can regenerate body parts, mammals generally cannot, and cancer progression is complex, involving mutations rather than a strict stem cell hierarchy.

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

Most adrenal cortex tumors are benign and non-secreting, but proper diagnosis and treatment are important due to the rare possibility of cancer.

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.

Caffeine improves hair growth, thickness, and reduces shedding.

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

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

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

Mirex seems to promote a unique group of skin cells different from those affected by another tumor promoter, TPA.

The study suggests that motor neurons created from stem cells of patients with spinal and bulbar muscular atrophy show signs of the disease, including changes in protein levels and cell functions.

Scientists turned mouse stem cells into skin cells that can grow into skin layers and structures.

Parthenolide promotes hair growth in mice and may influence pathways related to male pattern baldness.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

Inactive hair follicle stem cells help prevent skin cancer.