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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.

New findings explain how genetic changes, body clocks, and certain molecules affect tissue response to stress hormones.

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

The conclusion is that genetic changes in the glucocorticoid receptor can lead to conditions affecting stress response, immunity, and metabolism, requiring personalized treatment.

New method finds genetic links between Type 2 Diabetes and Prostate Cancer not seen before.

Epidermolysis bullosa is a genetic disease causing fragile skin and blisters in both animals and humans.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

Some families have a genetic condition where they are born with irregular scalp defects.

Nellore cattle have genetic variations linked to their adaptation to tropical environments.

The conclusion suggests that PCOS may persist due to genetic traits that, while harmful for female fertility, could have provided survival and reproductive benefits to males.

A rare genetic skin condition usually affecting males was found in a 9-year-old girl.

CAH is a genetic disorder affecting cortisol production and causing hormonal imbalances, with treatment and diagnosis varying by form and symptoms.

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

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

Antiandrogen therapy helps treat genetic hair loss.

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

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

Monilethrix is a rare genetic hair disorder that's hard to treat.

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

The study found genetic differences related to hair development that may explain hair loss in a patient with Trichorhinophalangeal syndrome type I.

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

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.

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

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

Recent findings suggest that genetic factors, immune system issues, and skin cell defects might contribute to the development of hidradenitis suppurativa.

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

A certain genetic variation is linked to a higher risk of polycystic ovarian syndrome.

Monilethrix is a genetic hair disorder causing fragile, beaded hair with no effective treatment.

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.