Search

everythinglearnresearchcommunity

for

Search:↓

Scientists have created a new hair loss treatment using ultrasound to deliver gene-editing particles, which resulted in up to 90% hair regrowth in mice.

Drug repositioning is becoming more targeted and efficient with new technologies, offering personalized treatment options and growing interest in the field.

Mutations in certain receptors can cause diseases and offer new treatment options.

Blocking the FGF5 gene in sheep leads to more fine wool and active hair follicles due to changes in certain cell signaling pathways.

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

A specific protein in chicken embryos links early skin layers to feather development.

Forensic medicine is crucial for justice and needs continuous innovation and technology integration.

Immune cells are essential for early hair and skin development and healing.

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

Mutations in the NR3C1 gene cause a rare condition that affects hormone signaling and can lead to various symptoms, with dexamethasone as a treatment option.

Ichthyosis with confetti is a genetic skin disorder with consistent ectodermal malformations and various KRT10 gene mutations.

Forensic DNA Phenotyping accurately predicts physical traits and is used in investigations, but needs more diverse population data for confirmation.

A mutation in the IKZF1 gene causes immune system overactivity, linked to autoimmune diseases like lupus.

Congenital Adrenal Hyperplasia is a rare inherited disease causing hormone imbalances, affecting growth, fertility, and heart health, diagnosed through blood tests and treated with medication and lifestyle changes.

The TRPV3 gene variant may cause the long-haired suri alpaca coat.

Finasteride may cause lasting sexual and mental health issues, and genetic screening could help prevent them.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

Using CRISPR for gene editing in the body is promising but needs better delivery methods to be more efficient and specific.

Mutations in the androgen receptor gene cause Androgen Insensitivity Syndrome, affecting sexual development.

Mice with LSS deficiency showed hair loss and cataracts, similar to humans, and can help in understanding and treating this condition.

A patient with Werner syndrome showed a range of aging-like symptoms and metabolic issues, underscoring the need for early detection and treatment.

Molecular diagnostics help identify genetic defects causing endocrine diseases, improving diagnosis and treatment options.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

A new mouse mutation causes skin and hair defects due to a gene change.

Hair follicle bumps with stem cells might contribute to permanent hair loss by getting disconnected due to scarring.

Aging mice have slower hair regeneration due to changes in signal balance, but the environment, not stem cell loss, controls this, suggesting treatments could focus on environmental factors.

Hair restoration surgery can have complications; success depends on patient education, careful planning, and proper execution.

Male hair loss is caused by inactive hair follicle stem cells.

Smad1 and Smad5 are essential for hair follicle development and stem cell sleepiness.

A mutation in the Soat1 gene causes hair structure defects and other health issues in AKR/J mice.