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Genetic defects in testosterone production can cause hormonal and developmental disorders, and more research is needed to understand androgen regulation and develop safer treatments.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Shorter PSADT after prostate surgery is linked to higher risk of death.

LPA3 is crucial for embryo implantation and links LPA to prostaglandin signaling.

Hairless protein is crucial for healthy skin and hair, and its malfunction can cause hair loss.

Oncogenic K-ras causes rapid cancerous changes in the mouth's lining.

Inhalation therapy may repair and protect elastin in the lungs of COPD patients.

Wnt-10b is important for keeping mouse skin cells healthy for hair growth.

The conclusion is that many small genetic variations influence claw disorders in cows, and using genomic selection could help reduce these disorders.

Sons of mothers with polycystic ovary syndrome (PCOS) have a higher risk of obesity and insulin resistance, possibly due to certain genes and factors passed down from their mothers.

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

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

The document concludes that managing Dunnigan-Type Familial Partial Lipodystrophy involves treating associated health issues and using medications like metformin and leptin replacement.

Sostdc1 controls the size and number of hair and mammary gland structures.

Metabolism plays a key role in determining stem cell fate.

Frizzled 3 and Frizzled 6 together control the orientation of mouse hair follicles.

The workshop discussed the role of a protein called calreticulin in health and disease, its potential as a treatment target, and its possible use as a disease marker.

Lower SMAD2/3 activation predicts more severe skin cancer.

PCOS causes infertility mainly due to hormonal imbalances, insulin resistance, and chronic inflammation.

Hair microscopy is a simple and cost-effective method to help diagnose systemic diseases in children.

T-regulatory cells are important for skin health and can affect hair growth and reduce skin inflammation.

Some women with PCOS have rare genetic variants linked to the condition.

Certain skin proteins can form anchoring structures without the protein AMACO.

Genetic risk for PCOS can affect children's growth, metabolism, and development from early life into adulthood.

The Hedgehog signaling pathway is important for skin and hair growth and can lead to cancer if it doesn't work right.

Notch signaling is essential for healthy skin and hair follicle maintenance.

Disrupting β-catenin signaling in certain cells causes anorectal malformations.

Sex hormones like estrogen and testosterone may affect COVID-19 severity differently in men and women, potentially influencing prevention and treatment strategies.

New genetic mutations linked to rare skin disorders were found in three newborns.

Hedgehog signaling in certain cells is crucial for hair growth during wound healing.