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The conclusion is that genetic differences affect how the cochlea heals after hair cell loss, which may challenge the creation of hearing loss treatments.

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

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

A new genetic mutation in the TRPV3 gene causes Olmsted-like syndrome in a Mongolian family.

Mouse models help understand alopecia areata and find treatments.

The study found that genetic differences related to hair growth and other traits help cashmere goats adapt to high-altitude environments.

Three siblings with a genetic form of rickets showed different symptoms of the disease.

The document concludes that various findings in rheumatology offer insights into disease severity, treatment responses, and potential risks in medication, with some limitations due to unspecified participant numbers.

Scientists found new genetic areas that affect how rice root hairs grow and develop.

The meeting presented new findings on hair stem cells, pigmentation, genetics, and modern hair treatment techniques.

A specific genetic marker is linked to male pattern baldness in Han Chinese men.

The QuantAnts machines can find cancer markers and create CRISPR targets for them.

A specific genetic deletion in goats affects cashmere yield and thickness.

The document highlights advancements and findings in dermatology, including AI use, disease prevention, treatment efficacy, and the impact of conditions on patients' lives.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

Blocking IL-1 could help treat some hair loss conditions; alopecia affects liver detox systems; spironolactone is better than finasteride for female hair growth; focusing on the catagen hair phase could lead to new alopecia treatments.

The document concludes that understanding genetic mutations in the PI3K-AKT-mTOR pathway can lead to better diagnosis and treatment for certain genetic skin disorders.

A patient with a larger than usual genetic mutation had a broader range of symptoms for a muscle disease.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

Blood tests can help understand the genetic differences in people with alopecia areata, including how severe it is and if it's inherited.

Boxer dogs may have a genetic skin condition that worsens seasonally and can be treated with certain medications.

Alopecia areata involves complex immune and genetic factors, with potential treatment targets identified, but more research is needed.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

Two patients with the same genetic mutation had both blistering skin and easily pulled out hair.

Men with thinner hair from genetic hair loss may be more likely to have an enlarged prostate.

The document summarizes skin and immune system disease findings, especially related to AIDS, from the 1980s.

Hair count is important to distinguish between genetic hair thinning (Androgenetic Alopecia) and hair thinning caused by disrupted hair growth (Chronic Telogen Effluvium).

A mother's diet at conception can cause lasting genetic changes in her child.

Giving a special protein to dogs with a certain genetic disease improved their symptoms but didn't help with hair growth.

Certain mouse strains develop a skin condition similar to a human hair loss disease due to genetic defects.