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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.

Genes and hormones cause hair loss, with four genes contributing equally.

Measuring reproductive hormones in brown bear hair could help identify their sex and reproductive state, but better collection methods or lab techniques are needed.

New treatments for male hair loss show promise but need more research for safety and effectiveness.

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

A gene mutation causes woolly hair in a Syrian patient.

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

Deleting the Trf1 protein in mice is safe and may help prevent cancer without major side effects.

Pangolins have lost some skin-related genes, but kept others, leading to their unique scales and skin features.

Pangolins have lost some skin-related genes, but kept others, showing complex skin evolution.

PCOS is a major cause of infertility in women of childbearing age.

The analysis aims to identify the most effective and safest treatments for alopecia areata.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

Early diagnosis and genetic evaluation of ADULT syndrome are crucial to reduce stress and medical costs.

Three specific genetic variants cause severe skin issues in children with EBS, highlighting the need for early genetic screening.

Tandem repeats significantly influence hair color, especially darker shades, across different ancestries.

Comprehensive screening for infections is crucial before starting JAK inhibitors in alopecia areata patients.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

Metatrials could improve clinical research in nephrology by speeding up data collection and overcoming challenges like patient recruitment.

The man has a genetic skin condition called pachyonychia congenita.

People with pattern hair loss have higher polyamine levels in the top of their head compared to the back.

Genetically repaired stem cells may treat certain genetic diseases, Th17 cells are key in fighting systemic fungal infections, hair loss in AGA is due to progenitor cell loss, and α-synuclein transfer might contribute to Parkinson's disease progression.

Understanding where cancer cells come from helps create better prevention and treatment methods.

Colorectal cancer development involves both genetic changes and epigenetic alterations like DNA methylation and microRNA changes.

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.

Fibrodysplasia ossificans progressiva is a rare genetic disorder that causes extra bone growth and symptoms of premature aging.

Keratosis pilaris is often linked to genetic mutations and causes skin and hair abnormalities, regardless of those mutations.

Thiopurines help treat IBD but require genetic testing to avoid side effects.

No link found between specific genes and female pattern hair loss.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.