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

RNA can be extracted from horsehair roots for analysis.

Crossbreeding improves goat fiber quality, and specific genes affect hair traits and color.

A genetic variant in the androgen receptor gene increases heart disease risk in women but not in men.

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

Pigs without the Hairless gene showed skin and thymus changes, useful for studying human hair disorders.

A specific RNA modification in cashmere goats helps activate hair growth-related stem cells.

The document concludes that specific hair and blood vessel abnormalities in infants with seizures and developmental issues may indicate Menkes disease, which lacks a cure and is often fatal by age 3.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

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

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

Activating β-catenin in mammary cells leads to changes that cause early-stage abnormal growths similar to skin structures.

The baby’s hair loss was due to a rare genetic condition, not treatable by usual methods.

Different forms of FGF5 either promote or inhibit hair growth.

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

Scientists made a mouse that shows how a specific protein in the skin changes and affects hair growth and shape.

Personalized thiopurine dosing based on NUDT15 genotyping can improve long-term outcomes for ulcerative colitis and Crohn's disease patients.

Hutchinson-Gilford Progeria Syndrome causes rapid aging from a genetic mutation, with no cure but ongoing research into potential treatments.

Certain genetic variations in IL-16 may increase the risk of alopecia areata.

MOF controls skin development by regulating genes for mitochondria and cilia.

The document concludes that the development of certain tumors is influenced by genetic background and that a specific gene modification can lead to tumor regression and reduced growth.

Certain gene variations are linked to a higher risk of severe acne, suggesting a genetic influence on the condition.

Adverse events in lung cancer treatments increase fear, anxiety, and depression, with newer therapies causing fewer side effects.

Lichen Planopilaris is a hair loss condition best treated early with various medications, including hydroxychloroquine, to prevent permanent baldness.

The conclusion is that adult males with muscle weakness and hormonal imbalances should be tested for Kennedy's disease.

Lower adrenal hormone levels may cause hair loss in postmenopausal women, certain patterns help diagnose nail cancer, and a gene variant linked to higher skin cancer risk in kidney transplant patients suggests monitoring folate levels.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

A new TP63 mutation was found in a baby with EEC syndrome, showing the need for TREC testing to check for immune issues.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.