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Lipase H is important for hair follicle function and shaping hair fibers.

Women with nonclassical congenital adrenal hyperplasia may have a higher risk of fertility issues and miscarriages, and should get genetic counseling.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

Genetic testing is crucial for diagnosing congenital atrichia, a rare condition causing irreversible hair loss.

The conclusions are: fecal short-chain fatty acids may help prevent cancer, fiber intake can reduce obesity, weight loss is hard for obese people, low BMI cancer patients are more prone to chemotherapy side effects, intermittent fasting benefits gut health, cherry laurel has health benefits in rats, certain gene variations can increase stress in hair loss patients, fecal acids can affect blood sugar levels, cold agglutinin can affect blood test results in autoimmune patients, and people with Crohn's disease have higher levels of a certain chemical in their blood.

A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

Primary cilia affect the size and oil production of eye glands but not the oil's makeup.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

Mutations in the FOXN1 gene cause severe immune issues but don't affect hair and nails.

Patients with certain FoxN1 gene mutations have severe immune issues but normal skin and hair.

The meeting highlighted the genetic basis of female pattern hair loss and various skin health insights.

The workshop highlighted the genetic links and psychological impacts of hair loss and skin disorders.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

A 37-year-old male with severe skin and internal issues has a rare inherited skin condition called dystrophic epidermolysis bullosa.

The document concludes that patient outcomes for Congenital Adrenal Hyperplasia are often not ideal because of poor management and a need for better diagnosis and treatment methods.

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

The CAP1 gene helps control ammonium levels and is necessary for the proper growth of root hairs in Arabidopsis.

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

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

The conclusion suggests that prostate cancer should be classified by castration status and that new therapies targeting androgen receptor signaling show promise.

Some congenital hair disorders improve in childhood or with treatments like minoxidil and retinoids, while others like Netherton syndrome and trichothiodystrophy have a poor prognosis.

A specific gene variant is linked to a higher risk of hair loss from chemotherapy in breast cancer patients.

A specific gene mutation causes congenital hair loss.

Genes linked to fibrosis are more active in people with central centrifugal cicatricial alopecia.

Inhibiting AP1 in mice skin causes structural changes and weakens the skin barrier.

A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

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

Certain genes are more active in baby scalp cells and can help grow hair when added to adult mouse skin cells.

The ACE1 gene variant doesn't affect long-COVID symptoms.

Different ACE2 gene versions may affect COVID-19 impact based on age and suggest some hair loss drugs could be potential treatments.