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An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

CRISPR/Cas9 has improved precision and control but still faces clinical challenges.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

Hair loss in women often doesn't follow a pattern, isn't linked to age, may be genetic, and can be related to thyroid issues or other health factors.

Genes related to pigmentation, body rhythms, and behavior change during hares' seasonal coat color transition, with a common genetic mechanism in two hare species.

Scientists developed a method to grow human fetal skin and digits in a lab for 3-4 weeks, which could help study skin features and understand genetic interactions in tissue formation.

Skin reactions to drugs are common and can be deadly, usually requiring stopping the drug and may be better prevented with genetic testing in the future.

The document concludes that new treatments for hair loss may involve a combination of cosmetics, clinical methods, and genetic approaches.

Dermatologists give better information on pathology forms, hypersensitivity vasculitis is a common skin issue, misdiagnoses can occur, and various skin conditions are linked to loss of elastin or genetic factors.

The April 2014 issue of "Fertility and Sterility" discussed various reproductive health topics, including hormone therapy benefits, sperm and genetic factors in male infertility, and the link between PCOS and diabetes.

Researchers found new hair and nail genes, how hair reacts to UV, differences in white and pigmented hair growth, nerve changes in alopecia, treatments for baldness and alopecia, a toenail condition linked to a genetic disorder, and that nail fungus is more common in people with psoriasis.

Different skin stem cells help heal wounds, with hair follicle cells becoming more important over time.

Genetics affect early female hair loss, severity depends on duration, and low ferritin levels not significant.

Methotrexate effectively treated a 2-year-old's generalized pustular psoriasis without side effects.

About 15% of adolescent girls in a region of India have Polycystic Ovarian Syndrome, which is more common in those born by cesarean, with wisdom teeth, or with central obesity.

Male and female hair loss have different genetic causes.

The conclusion suggests that early signs of hidradenitis suppurativa may start in the hair follicle, with genetic and immune factors playing a role, highlighting the need for more research on the hair follicle's immune system.

The book is a valuable guide for hair restoration surgeons.

Alopecia areata in infants may be more common than previously thought.

Six genetic conditions are often linked to complete scalp hair loss in children.

Keratins are important for skin cell health and their problems can cause diseases.

Kids with early graying hair often have low levels of calcium, ferritin, and vitamin D3.

DNA phenotyping helps predict physical traits from DNA with varying accuracy and requires careful ethical and legal handling.

New hair loss treatments may include topical medications, injections, and improved transplant methods.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

People with Mucopolysaccharidoses often have skin problems like thick skin and extra hair, and recognizing these can help diagnose and treat the condition early.

Two gene variations, rs6493497 and rs7176005, may be linked to female hair loss in Chinese people.

The study found that a specific genetic variation in the TNFα gene is significantly linked to Alopecia Areata in the Jordanian Arab population.

Genetic mutations that disrupt homocysteine breakdown lead to increased damage in mouse hair keratin.

Hair diameter and curvature are mostly determined by genetics.