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

Albumin and prednisone improved symptoms in a woman with Cronkhite-Canada syndrome, revealing potential genetic causes.

Hairless mammals have genetic changes in both their protein-coding and regulatory sequences related to hair.

Cantú syndrome is caused by mutations in the ABCC9 gene.

Both gene and non-gene areas of DNA evolved to make some mammals hairless.

Hairlessness in mammals is due to complex genetic changes in both genes and regulatory regions.

Msx and Dlx genes are crucial for development, controlling cell behaviors like growth and differentiation through their roles as gene regulators.

Diphenyl cresyl phosphate has low toxicity but can harm the liver, kidneys, adrenal glands, and testicles at high doses.

Standardized procedures are crucial for collecting and preparing biological samples to ensure accurate clinical metabolomics results.

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

The Asiatic lion has very low genetic diversity and unique genetic traits, highlighting the need for its conservation.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

MILL molecules are unique immune proteins in mice that don't need TAP to appear on cell surfaces.

Alopecia areata is likely an autoimmune disease with unclear triggers, involving various immune cells and molecules, and currently has no cure.

Researchers found 15 new genetic links to skin traits in Japanese women.

Researchers found 71 genetic regions linked to male pattern baldness, which account for 38% of its genetic risk.

Researchers found a gene mutation responsible for a rare hair loss condition.

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

Shift work disrupts the body's natural clock, leading to health problems.

Enzymes called PADIs play a key role in hair growth and loss.

Alopecia areata is an incurable autoimmune condition causing hair loss, with research aiming for better treatments.

Many infertile women with PCOS in Central Vietnam have metabolic or insulin resistance syndrome, with obesity and older age increasing the risk.

The safety and effectiveness of gender-affirming treatments for children are uncertain, with potential long-term risks like infertility.

The document concludes that new methods improve the accuracy of diagnosing scalp alopecia and challenges the old way of classifying it.

The most common hair loss type at specialist clinics is androgenetic alopecia, especially in younger men, followed by alopecia areata and telogen effluvium, with differences seen across regions.

The conclusion is that accurate diagnosis of different types of hair loss requires careful examination of tissue samples and understanding of clinical symptoms.

New techniques have enhanced our understanding of how stem cells function and the role of mutations in aging tissues, which may influence future cancer therapies.

Insulin resistance contributes to hormone imbalances in many women with polycystic ovary syndrome.

Yellow dots and short vellus hairs are key signs for diagnosing alopecia areata using trichoscopy.

The article concludes that early diagnosis and lifestyle changes can prevent complications from high uric acid levels.