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A gene variant increases the risk of a type of hair loss by affecting hair protein production.

Researchers found WNT10A to be a key gene in developing goat hair follicles.

The UD-PrOZA program successfully diagnosed 18% of adult patients with rare diseases, often using genetic testing.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

Blocking YAP/TAZ could be a new way to treat skin cancer.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Genes and epigenetic changes are important in the development of Polycystic Ovary Syndrome.

Researchers made a mouse model with curly hair and hair loss by editing a gene.

SGK3 is essential for proper hair growth and health.

Dermatologists diagnose and manage melanoma more effectively than general practitioners.

Genes play a significant role in male-pattern baldness, and understanding them could lead to new treatments and insights into related health issues.

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

Mice treatments didn't grow hair, a patient treatment may affect immune response, and people with hair loss often feel anxious or depressed.

The vitamin D receptor is crucial for bone health and affects various body systems, with mutations potentially leading to disease.

The document concludes that insulin resistance is key in PCOS development and early treatment is crucial to prevent complications.

BAY 43-9006 helps control kidney cancer growth but doesn't significantly increase overall survival.

The Rotterdam Study aims to understand various diseases in older adults.

Mutations in the PADI3 gene are linked to a higher risk of scarring hair loss in women of African descent.

Mice studies show that Protein Phosphatase 2A is crucial for cell growth, development, and disease prevention.

The document concludes that recognizing and properly diagnosing lipodystrophy syndromes is crucial for effective management and treatment.

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

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

Hair diversity is influenced by complex genetics and environmental factors, requiring more research for practical solutions.

FGF5s can block the effects of FGF5, which may help control hair growth in cashmere goats.

Parathyroid hormones are important for hair growth, but their use in treating hair loss from chemotherapy is still uncertain.

Certain genetic variants increase the risk of resistance to hormone therapy in prostate cancer patients.

Genetic variations affect dutasteride treatment response for male pattern hair loss.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

Tandem repeats significantly influence hair color, especially darker shades, across different ancestries.