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Certain genetic variations are linked to higher liver enzyme levels in patients treated for chronic hepatitis C with specific drugs.

Molecular diagnostics help identify genetic defects causing endocrine diseases, improving diagnosis and treatment options.

Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

Combining genetic and physical trait analysis improves diagnosis accuracy for monogenic diabetes.

The study developed a 3D model that closely imitates remaining ovarian cancer after treatment and identified a potential drug targeting resistant cancer cells.

A genetic mutation linked to longer life and less disease was found in the Amish, and a drug is being developed to replicate these benefits.

Some people with the skin color loss condition, vitiligo, also develop the skin inflammation condition, lichen planus, possibly due to local trauma, sun damage, or genetic factors.

Rare genetic variants in 125 genes are linked to male-pattern hair loss.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

Certain genetic variations in the AR and ERβ genes can affect androgen levels in women.

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 71 genetic regions linked to male pattern baldness, which account for 38% of its genetic risk.

New genetic discoveries in alopecia areata could lead to better treatments.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

Trichilemmal carcinoma shares genetic changes with other skin cancers, suggesting similar causes and potential treatments.

The conclusion is that hair loss from CCCA may be genetic and not solely caused by hair grooming practices.

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.

Researchers found a genetic region that influences the number of coat layers in dogs.

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

Researchers found two new genetic variants linked to Alzheimer's disease.

Researchers found genes and genetic variants linked to sheep wool and skin wrinkles.

Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

Researchers created a genetic library from a cashmere goat's skin and found new genes linked to hair growth.

Certain genetic variations in the A2M gene are linked to better milk quality in Murrah buffaloes.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

The most different genetic segment between Africans and East Asians is the EDA2R/AR region, with two main types influenced by population changes and natural selection, and linked to baldness.

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

Men with high genetic risk for Polycystic Ovary Syndrome (PCOS) have increased chances of obesity, type 2 diabetes, heart disease, and hair loss, showing PCOS risk factors can affect both genders.

A new genetic model may improve treatment and diagnosis for certain inherited skin diseases.