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Scientists found a gene in mice that causes early hearing loss.

Rapamycin reduces age-related hearing cell loss in mice, but acarbose does not.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

Mutations in the PTPRQ gene cause significant balance issues in mice due to hair bundle defects in the inner ear.

Surface Plasmon Resonance is a useful tool for studying protein interactions and has potential for future technological advancements.

Blocking adenosine A2B receptor may prevent or treat hearing loss.

Recent selection on immune response genes was identified across seven ethnicities.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Using CD123 to detect certain immune cells helps diagnose a type of hair loss condition.

A deletion in the CDH3 gene causes a rare disorder with short hair and vision loss.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Three characteristics of plasmacytoid dendritic cells help tell apart lupus-related hair loss from LPP.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

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

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

The research found that a specific gene mutation causes fewer hair follicles and disrupted hair growth cycles, leading to thin and short hair in people with Hypotrichosis with Juvenile Macular Dystrophy.

P-cadherin is important for hair growth and health, and its problems can cause hair and skin disorders.

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

Combining skin tissue pathology with genetics has greatly improved the diagnosis and understanding of certain skin diseases.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

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

Different types of resting melanocyte stem cells have unique characteristics and vary in their potential to become other cells.

The study found a link between the severity of Lichen Planopilaris seen by doctors and the details seen under a microscope, and created a new way to measure this severity.

P-cadherin is crucial for hair follicle pigmentation but not skin pigmentation.

Plasmacytoid dendritic cells are a key factor in causing hair loss in alopecia areata and could help differentiate it from other hair loss conditions.

A woman's hair loss worsened after starting hepatitis C treatment due to immune changes in her hair follicles.

Higher minoxidil dose helps hair growth in non-responders without side effects.

Chemotherapy and radiation therapy cause skin and hair damage by altering gene expression and signaling pathways.