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Finasteride may help reduce tic severity in male Tourette syndrome patients.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in patients with Tourette syndrome.

Finasteride may help reduce symptoms in male Tourette syndrome patients.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

The meeting highlighted the importance of genetic testing and multidisciplinary approaches in pediatric dermatology.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

Wild African goats have genetic adaptations for surviving harsh desert conditions.

Organoids help study and treat genetic diseases, offering personalized medicine and therapy testing.

Hidradenitis suppurativa might be a type of autoinflammatory skin disease.

Pangolins have lost some skin-related genes, but kept others, showing complex skin evolution.

The study concluded that specific proteins are necessary to maintain the structure that holds epithelial cells tightly together.

A boy with a new NR5A1 gene mutation has a sex development disorder without affecting his adrenal glands.

An American Bully with a genetic skin condition improved significantly with specific topical treatments.

Researchers found an RNA transcript that might help control a growth factor linked to tumor development.

The genes KRT25 and SP6 affect curly hair in horses, with KRT25 also causing hair loss. If both genes are mutated, the horse gets curly hair and hair loss. KRT25 can hide the effect of SP6.

Scientists are still unsure what triggers the immune system to attack hair follicles in Alopecia areata.

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

Melatonin receptors in hair follicles help regulate hair growth and could treat hair loss.

The document concludes that understanding sulfation biology is crucial for creating treatments due to its importance in biological functions and disease.

Chicken feather gene mutation helps understand human hair disorders.

Enzymes are classified into six types and are essential for many biological processes, with only a few targeted by drugs.

Certain genetic variations in OCT1 may improve insulin sensitivity with metformin in women with PCOS.

Kir6.1 mutations in Cantú syndrome increase channel sensitivity and hyperpolarization, while SUR2B mutations do not.

The document concludes that more research is needed to reduce frequent hospital visits, addiction medicine education improves with specific training, early breast cancer surgery findings are emerging, nipple smears are not very accurate, surgery for older melanoma patients doesn't extend life, a genetic condition in infants can often be treated with one drug, doctors are inconsistent with blood clot medication, a certain gene may protect against cell damage, muscle gene overexpression affects many other genes, and some mitochondrial genes are less active in mice with tumors.

African American men with prostate cancer have more androgen receptor mutations, which may lead to more aggressive cancer compared to Caucasian American men.

CD98hc's role in skin health decreases with age.

The document concludes that various signaling pathways and genetic factors are crucial for chicken feather development, affecting poultry quality.

The JAK/STAT pathway is important in cell processes and disease, and JAK inhibitors are promising for treating related conditions.

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

Combining genetic and physical trait analysis improves diagnosis accuracy for monogenic diabetes.