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Removing the ATR gene in adult mice causes rapid aging and stem cell loss.

Quick treatment of hair disorders in teenage girls is important because of the emotional effects.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

The document concludes that Cutaneous Lupus Erythematosus has different forms, is influenced by genetic and environmental factors, and can be treated with various medications, but more targeted therapies are needed.

The document explains how the male reproductive system works, its role in making testosterone, and how conditions like obesity can disrupt it, leading to low testosterone and fertility issues.

New genes and pathways are important for testosterone production and male sexual development.

Researchers developed a way to study human body clocks using hair tissue, which works similarly in both healthy and dementia patients.

Oncogenic K-ras causes rapid cancerous changes in the mouth's lining.

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

Deleting MED1 in skin cells causes hair loss and skin changes.

A woman with acromegaloidism and normal growth hormone levels had a rare X-Tetrasomy, suggesting a need to study X-chromosome genes for their role in growth and facial development.

The document is a detailed guide on skin conditions and treatments for dermatologists.

The follicular unit extraction method for hair transplants is a technique with benefits and drawbacks.

Stopping forehead irritation and using hydrocortisone helped a man's skin, Martinique has lower melanoma rates, a man had an allergy to a specific antifungal, another had unexplained cysts, certain drugs can cause skin reactions without always being interrelated, a link between Fanconi anemia and a skin condition was suggested, high levels of a certain protein may play a role in a type of psoriasis, and there's a need to study the connection between scalp pain and hair loss.

Men with a certain type of hair loss often use facial moisturizers, and a specific antibiotic treatment may help another hair condition.

The scraggly mutation causes hair loss and skin defects in mice.

Acute leukemias with the Philadelphia chromosome may be biphenotypic, and identifying this is important for proper treatment.

Frontal Fibrosing Alopecia is a hair loss condition mainly affecting postmenopausal women, with unclear causes and various clinical patterns.

A 12-year-old boy with a rare genetic condition has progressive hair loss with no effective treatment.

The Lanceolate hair-J mutation in mice mimics human hair disorders like Netherton's syndrome.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

A gene mutation in mice causes permanent hair loss and skin issues.

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

Hair problems can be caused by genetics or the environment, and treatment should focus on the cause and reducing hair damage.

Mutant mice help researchers understand hair growth and related genetic factors.

Over half of the children had abnormal hair under a microscope, with many having genetic hair conditions.

Early diagnosis and tailored treatments are crucial for managing ichthyosis syndromes with hair abnormalities.

Skin abnormalities can indicate immunodeficiency due to shared origins with the immune system.

Trichoscopy is a quick and easy way to diagnose most genetic hair problems without invasive methods.