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The document suggests treating individuals with nonclassic congenital adrenal hyperplasia who show symptoms, especially those related to excess male hormones.

The document explains different types of hair loss, their causes, and treatments, and suggests future research areas.

Human enzymes can detoxify harmful substances but might also increase their cancer risk.

Obesity changes androgen levels in women with PCOS, leading to higher testosterone relative to androstenedione.

Acne is a common skin condition linked to diet, hormones, and genetics, and early treatment can prevent scarring.

The transgene likely activated an oncogene or interrupted a tumor suppressor gene, causing melanoma in mice.

The document concludes that more research is needed to better understand and treat primary cicatricial alopecias, and suggests a possible reclassification based on molecular pathways.

Men with severe hair loss may have a higher risk of heart disease.

Kennedy's disease leads to muscle weakness and sensory issues, has no cure but manageable symptoms, and future treatments look promising.

People with myotonic dystrophy type 1 have a higher chance of getting skin tumors, including melanoma.

The research concluded that selection significantly shaped the genetic variation of the X chromosome, with certain regions affected by past selective events.

Blocking certain immune signals can reduce skin damage from radiation therapy.

The study found that Keratosis Pilaris Atrophicans is a genetic skin condition that starts in childhood, involves inflammation and scarring, and current treatments are only somewhat effective.

No clear link between specific gene and hair loss in Mexican brothers.

Environmental factors like smoking, UV exposure, and poor diet contribute to hair loss and graying, and lifestyle changes can help manage it.

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

Lichen planus pigmentosus causes dark skin patches and is treated by avoiding triggers and using anti-inflammatory medications.

Low-coverage sequencing is a cost-effective way to identify genes related to wool traits in rabbits.

Some women with PCOS have rare genetic variants linked to the condition.

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

Genes related to keratin, skin cell differentiation, and immune functions are key in hedgehog skin and spine development.

The study suggests that a specific gene variation and higher gene activity are linked to increased baldness in Egyptian men.

Researchers found a genetic region that influences the number of coat layers in dogs.

Bald thigh syndrome in sighthounds is caused by structural defects in hair shafts due to downregulated genes and proteins.

Alopecia areata, a type of hair loss, is likely an autoimmune disease with a genetic link, but its exact cause is still unknown.

Genetic mutation and carcinogen treatment are both needed for skin cancer to develop in these specific mice.

Scarless healing is complex and influenced by genetics and environment, while better understanding could improve scar treatment.

The research identified key proteins that affect wool fiber thickness in Angora rabbits.

The conclusion is that obesity should be managed with a slow, balanced approach to diet and exercise, with medication and surgery as additional options, and education and access to care are important.

In vivo lineage labelling is better than in vitro methods for identifying and understanding stem cells.