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Isoallopregnanolone may be a safe and effective treatment for reducing tics in a mouse model of Tourette syndrome.

Removing myelin protein zero-like 3 in mice leads to better metabolism and resistance to obesity.

Researchers developed a way to study human body clocks using hair tissue, which works similarly in both healthy and dementia patients.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

iPSCs help understand and treat neurodevelopmental disorders.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

A peptide from hair follicle stem cells can boost hair growth.

NIPT can help detect potential maternal cancer, and GIPXplore can identify immune diseases in pregnancies.

Harlequin mutant mice have hair loss due to low AIF protein levels and retroviral element activity.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

Pantaneiro sheep have more genetic diversity than Texel sheep, with potential for future research in Brazilian farming.

Newborn screening and gene therapy are expected to improve outcomes for Omenn syndrome patients.

Low-dose radiation therapy may improve brain function in some Alzheimer's patients and is generally well-tolerated.

Most 46XX CAH patients have female identity, but a few identify as male and may need treatment and surgery.

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

ARWH is a rare hair disorder with no cure, but potential treatments include minoxidil and other therapies.

Adrenal disorders often cause high blood pressure in young people.

Removing Sprouty genes in mice causes various hormone-related issues but does not increase cancer risk by one year of age.

HDAC6 helps keep ovarian follicles dormant, extending female fertility.

Vimentin is crucial for wound healing, cell growth, and managing immune responses.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

Chrousos Syndrome is caused by mutations that make the body less sensitive to glucocorticoids, leading to various symptoms and requiring high-dose treatment.

HNG may help prevent the negative effects of chemotherapy on sperm production and white blood cell counts.

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

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

Certain gene variants may contribute to high androgen levels in women with polycystic ovary syndrome.

Mice can correct hair follicle orientation without certain genes, but proper overall alignment needs those genes.

Some growth factors, while important for normal body functions, can cause diseases when not regulated properly.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.