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Researchers created a model to understand heart aging, highlighting key genes and pathways, and suggesting miR-208a as a potential heart attack biomarker.

High levels of testosterone and anti-Müllerian hormone before pregnancy are linked to a higher risk of newborns needing intensive care.

A20 protein is crucial for normal skin and hair development.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

WNT7A gene expression is higher in early stages of androgenetic alopecia, showing the role of WNT pathway, apoptosis, and inflammation in the disorder.

SA linked to mitochondrial issues and oxidative stress, while AGA involves disrupted hair growth genes.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

The research identified genes and pathways important for sheep wool growth and shedding.

Researchers identified genes and proteins that may influence wool thickness in sheep.

The research provides a gene-based framework for hair biology, highlighting the Hippo pathway's importance and suggesting links between hair disorders, cancer pathways, and the immune system.

Young women in West Bengal, India, with PCOS often have estrogen resistance, leptin receptor issues, folate deficiency, T2DM, and acanthosis, commonly linked to obesity.

SH-MSCs gel can effectively treat alopecia by increasing IL-10 and decreasing TNF-α gene expression.

Involucrin gene expression is controlled by specific proteins and signaling pathways.

Hidradenitis suppurativa is caused by genetic factors, inflammation, bacteria, hormones, and lifestyle factors like obesity and smoking.

Estrogens generally inhibit hair growth and improve skin quality, but their exact effects on hair follicles are complex and not fully understood.

Melanoma's complexity requires personalized treatments due to key genetic mutations and tumor-initiating cells.

Certain genes are linked to the quality of cashmere in goats.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

The congress highlighted new gene therapy techniques and cell transplantation methods for treating diseases.

The meeting highlighted the genetic basis of female pattern hair loss and various skin health insights.

Different types of skin cells have unique genetic markers that affect how likely they are to spread cancer.

Acne is caused by genetics, diet, hormones, and bacteria, with treatments not yet curative.

Hair diversity is influenced by complex genetics and environmental factors, requiring more research for practical solutions.

The research found that the gene activity in mouse skin stem cells changes significantly as they age.

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

Men with early balding showed higher levels of certain genes linked to hair loss and possibly prostate cancer.

Deleting the Far2 gene in mice causes sebaceous gland issues and patchy hair loss.

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.

Cholesterol sulfate buildup due to a genetic mutation disrupts the skin barrier, leading to the scaling skin seen in X-linked ichthyosis.