Search

everythinglearnresearchcommunity

for

Search:↓

Certain gene variations in the Vitamin D receptor may increase the risk of chronic hair loss.

Women with hair loss have more androgen receptors in certain hair follicles.

Feathers are useful for researching growth, regeneration, and the effects of treatments like chemotherapy on hair loss.

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

Longer TA repeats in the SRD5A2 gene may increase acne risk in Chinese people.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

5α reductase type 2 enzyme mutation and oxidative stress may increase androgenetic alopecia risk in Egyptians.

Some human genetic markers work for genetic studies in pig-tailed and stump-tailed macaques, which can help in their conservation.

WNT10B is linked to cancer development and affects survival and disease progression in various cancers.

Certain gene variations in AKT2 are more common in women with PCOS and are linked to higher levels of specific hormones and symptoms.

Men, especially older ones with health issues like prostate cancer, may have worse COVID-19 outcomes and could benefit from therapies targeting male hormones.

Australian court ruled that Bickfords did not infringe on Monster Energy's trade mark because Monster was not sold or known in Australia at the time.

Stress and alcohol affect brain chemicals differently in rats, mice, and humans, influenced by genetic differences.

Proper control of β-catenin activity is crucial for development and preventing diseases like cancer.

Men generally have more severe COVID-19 cases and higher death rates than women due to biological differences.

The conclusion is that individual differences in COVID-19 severity are influenced by factors like age, sex, race, and genetics, which are important for personalized medicine.

Despite progress in treatment, the exact cause of Alopecia areata is still unknown.

Some treatments work for common baldness, but there's less evidence for other hair loss types, and more research is needed.

Two siblings both had a rare case of alopecia areata at the same time.

RXRα is crucial for proper immune response and links diet to immune function.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

VPS13C variants are linked to more severe REM sleep disorder and faster progression to Parkinson's disease.

Genetic factors, skin barrier, immune function, and obesity influence risk of fungal skin infections.

PCOS involves immune and genetic factors, with key roles for T cells and specific genes.

Blocking IL-17a can improve age-related smell loss in mice.

Activating Kras in mouse skin causes excess skin and hair loss.

Reduced EGFR signaling delays hair cycle and reduces fat growth, but hair development remains normal.

The fuzzy gene is crucial for controlling hair growth cycles.

KRT71 gene variants may influence camel hair shape but don't fully explain it.

The KRTAP36-1 gene affects wool quality in Chinese Tan lambs.