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Mouse profilaggrin helps in skin cell differentiation and may be involved in calcium signaling.

Certain gene mutations can weaken the skin barrier and, when combined with environmental factors, lead to eczema and severe itching.

The conclusion is that androgenetic alopecia and senescent alopecia have unique gene changes, suggesting different causes and potential treatments for these hair loss types.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

A complex X chromosome rearrangement can increase the risk of multiple autoimmune diseases.

Recognizing oral symptoms can help diagnose and treat blood and nutritional diseases early.

SCD1 is crucial for skin health and overall energy balance.

Some skin conditions may increase the risk of heart disease, but are not yet included in cardiovascular prevention guidelines.

Stopping S100A3 activity slows down hair growth in mice.

Certain DNA variants can predict straight hair in Europeans but are not highly specific.

Mother and son diagnosed with a rare genetic hair loss condition with no effective treatment.

Hoxc13 gene affects wool length in Gansu alpine fine-wool sheep.

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.

Some hair loss disorders are caused by genetic mutations affecting hair growth.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

Mutations in the KRT85 gene cause hair and nail problems.

PPARγ is essential for maintaining healthy skin, controlling inflammation, and ensuring proper skin barrier function.

Disrupting the Flcn gene in mice causes early kidney cysts and tumors, which can be treated with rapamycin.

Researchers mapped and categorized specific keratin-associated protein genes on human chromosome 21q22.1.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

Hair loss gene found on chromosome 3q26.

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

A gene called HDAC9 might be a new factor in male-pattern baldness.

The gene for slick hair in Senepol cattle is located on chromosome 20 and may involve the SRD5A2 gene.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

A mutation in mice causes hair loss and immune problems.

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

The document concludes that the human keratin gene cluster is complex, with a need for updated naming to reflect over 50 functional genes important for hair and skin biology.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.