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Scientists found a new gene in a bacterium that can modify an immunosuppressant drug, potentially helping to treat hair loss.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

KIF18B is important for correctly positioning cell division machinery in skin cells, affecting hair follicle development.

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

The document concludes that there is a need for more research and regulation in dermatology, covering topics like latex allergy in children, the use of botulinum toxin, and treatments for skin conditions.

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

Catalytic antibodies are early indicators and active participants in the development of systemic lupus erythematosus.

OR2AT4 helps reduce aging and cell damage in human skin cells.

A second domain of high sulfur KAP genes on chromosome 21q23 is crucial for hair structure.

Most hair follicle stem cells do not protect their DNA by dividing it unevenly.

A mutation in mice causes hair loss and immune problems.

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

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

A new type of hereditary hair loss in a Chinese family is linked to chromosome 2p25.1–2p23.2.

New genes linked to male pattern baldness were found on chromosome 20p11.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

Certain genetic markers on chromosome 20 are linked to hair loss in the Han Chinese from Yunnan.

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

Loss of the Y chromosome and UTY gene activity increases cancer risk in men.

Certain genes and X chromosome patterns may significantly contribute to the development of hair loss.

Certain gene variations and irregular X chromosome activity may contribute to hair loss in women who can have children.

A 36-year-old person with a female appearance but male chromosomes was diagnosed with a rare enzyme deficiency affecting sexual development.

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.

Keratosis Follicularis Spinulosa Decalvans is a rare genetic disorder causing skin and hair issues, often inherited through the X chromosome.

Alopecia areata involves both innate and adaptive immunity, with specific genes linked to the disease.

Common variants in the Trichohyalin gene are linked to straight hair in Europeans.

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

The hr gene is crucial for skin and hair health, with mutations causing hair disorders.