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

Finger length ratios are not linked to the number of specific gene repeats affecting testosterone sensitivity.

The review found no clear link between vitamin D receptor gene variations and polycystic ovary syndrome.

Runx1 controls fat-related genes important for normal and cancer cell growth, affecting skin and hair cell behavior.

The 25Up study collected extensive data on mental disorders and related factors in Australian twins and siblings to investigate the genetics of psychiatric illnesses.

Patients with myotonic dystrophy often have skin problems that suggest early aging and vitamin D issues, and the severity of these problems is linked to their genetic condition and vitamin D levels.

Environmental factors like diet and vitamin levels, especially Vitamin D, can affect autoimmune diseases differently, with lifestyle changes potentially improving outcomes.

Certain genetic changes in the KAP22-1 gene are linked to better wool quality in Egyptian sheep.

African American women have a higher risk of preterm delivery than Caucasian women, and inflammatory stimuli affect gene expression in cells related to PCOS, showing a heightened inflammatory state in women with PCOS.

The Rotterdam Study found risk factors for elderly diseases, links between lifestyle and genetics with health conditions, and aimed to explore new areas like DNA methylation and sensory input effects on brain function.

Certain microRNAs are linked to various skin diseases and could be used to diagnose and treat these conditions.

HPV16 oncogenes disrupt the normal activity of hair follicle stem cells.

Low-coverage sequencing is a cost-effective way to find genetic factors affecting rabbit wool traits.

Genetic factors and diet significantly increase the risk of male pattern baldness.

A gene mutation in Lama3 is linked to a common type of hair loss.

Different genes cause Female Pattern Hair Loss compared to male hair loss, and treatments vary, but more research is needed to understand it fully.

Researchers found genes and microRNAs that control curly fleece in Chinese Tan sheep.

A specific gene variation is linked to a higher risk of polycystic ovary syndrome in Caucasian women.

Autism's genetics are linked with early age of puberty and less hair loss, but not with hormone levels or polycystic ovary syndrome.

Certain genes related to sulfur metabolism are more active during the growth phase of Cashmere goat wool, and melatonin might help this process.

Women with PCOS have distinct retinal changes compared to healthy women.

Genes related to calcium signaling and lipid metabolism are important for curly hair in Mangalitza pigs.

Leptin-deficient mice, used as a model for Type 2 Diabetes, have delayed wound healing due to impaired contraction and other dysfunctional cellular responses.

The we/we wal/wal mice have defects in hair growth and skin layer formation, causing hair loss, useful for understanding alopecia.

The conclusion is that PCOS is caused by ovarian sensitivity to hormones and disrupted hormone control, possibly due to ovarian factors, and more research is needed.

Aromatase gene variation may increase female hair loss risk.

Finasteride and dutasteride are effective for long-term treatment of enlarged prostates but have sexual side effects and a risk of high-grade prostate cancer.

Certain gene variations increase male hair loss risk, influenced by hormone levels.

Normal hair density and diameter ratios were established to help diagnose adult hair loss.

MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.